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Combined Registry for the clinical use of mechanical ventricular assist pumps and the total artificial heart: first official report--1986.
6(2)
68-70
The Journal of heart transplantation
[ { "affiliation": "", "forename": "W E", "identifier": "", "initials": "WE", "lastname": "Pae" }, { "affiliation": "", "forename": "W S", "identifier": "", "initials": "WS", "lastname": "Pierce" } ]
1987
3305831
D001243:Assisted Circulation / Q000009:adverse effects; D005260:Female; D016027:Heart Transplantation; D006354:Heart, Artificial / Q000009:adverse effects; D006353:Heart-Assist Devices / Q000009:adverse effects; D006801:Humans; D008297:Male; D009026:Mortality; D012042:Registries
D016428:Journal Article
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.079509Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Recovery of heart function following 24 hours preservation and ectopic transplantation.
5(4)
298-303
We examined the capacity of hearts injured during 24 hours of preservation to recover function over 96 hours when placed in an ectopic transplant configuration. Standard Langendorff techniques employing an intraventricular balloon and fixed perfusion pressure of 80 mm Hg were used to measure parameters of myocardial function, including maximal systolic pressure, left ventricular end diastolic pressure, and left ventricular balloon volume. Hearts preserved for 24 hours and held ischemic for 1 hour at room temperature exhibited significantly depressed contractility (maximal systolic pressure decreased by 26%) and diastolic compliance (left ventricular balloon volume decreased by 61%). During 96 hours in the ectopic transplant configuration, 24-hour preserved hearts recovered 52% of the lost diastolic compliance. These data demonstrate that 24-hour preserved and transplanted hearts recovered function over 96 hours.
The Journal of heart transplantation
[ { "affiliation": "", "forename": "J M", "identifier": "", "initials": "JM", "lastname": "Burt" }, { "affiliation": "", "forename": "D F", "identifier": "", "initials": "DF", "lastname": "Larson" }, { "affiliation": "", "forename": "J G", "identifier": "", "initials": "JG", "lastname": "Copeland" } ]
1986
3305821
D000818:Animals; D001794:Blood Pressure; D006321:Heart / Q000502:physiology; D016027:Heart Transplantation; D009200:Myocardial Contraction; D009926:Organ Preservation / Q000379:methods; D011817:Rabbits; D013318:Stroke Volume; D013997:Time Factors; D014184:Transplantation, Homologous / Q000379:methods
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D013487:Research Support, U.S. Gov't, P.H.S.
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[ { "agency": "NHLBI NIH HHS", "country": "United States", "grant_acronym": "HL", "grant_id": "HL31008" } ]
"2024-08-13T08:46:10.080248Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Combined transplantation of heart and liver from two different donors in a patient with familial type IIa hypercholesterolemia.
5(4)
327-9
A 12-year-old child with terminal ischemic heart disease as a result of homozygotous familial type IIa hypercholesterolemia received an orthotopic heart transplant and, 21 days later, an orthotopic liver transplant. Six months after heart transplantation, the patient is asymptomatic and evidences normal liver function and cholesterol levels; there are no signs of heart rejection. To our knowledge, this is the first instance of two-step heart-liver transplantation with organs from different donors.
The Journal of heart transplantation
[ { "affiliation": "", "forename": "D", "identifier": "", "initials": "D", "lastname": "Figuera" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Ardaiz" }, { "affiliation": "", "forename": "V", "identifier": "", "initials": "V", "lastname": "Martín-Júdez" }, { "affiliation": "", "forename": "L A", "identifier": "", "initials": "LA", "lastname": "Pulpón" }, { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Pradas" }, { "affiliation": "", "forename": "V", "identifier": "", "initials": "V", "lastname": "Cuervas-Mons" }, { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Burgos" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Arcas" }, { "affiliation": "", "forename": "F", "identifier": "", "initials": "F", "lastname": "Pardo" }, { "affiliation": "", "forename": "J A", "identifier": "", "initials": "JA", "lastname": "Cienfuegos" } ]
1986
3305826
D002648:Child; D003327:Coronary Disease / Q000209:etiology / Q000601:surgery*; D006085:Graft Survival / Q000187:drug effects; D016027:Heart Transplantation; D006801:Humans; D006938:Hyperlipoproteinemia Type II / Q000150:complications*; D007166:Immunosuppressive Agents / Q000627:therapeutic use; D016031:Liver Transplantation; D008297:Male; D014019:Tissue Donors
D002363:Case Reports; D016428:Journal Article
D007166:Immunosuppressive Agents
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.082324Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Inhibitory and cidal antimicrobial actions of electrically generated silver ions.
45(9)
779-84
One promising alternative to antibiotics in the treatment of localized infections is the generation of antimicrobial silver ions by the use of low intensity direct current from a pure silver anode implanted at the site of an infection. This study investigates the in vitro bacteriostatic and bactericidal properties of this system on a variety of organisms.
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
[ { "affiliation": "", "forename": "R E", "identifier": "", "initials": "RE", "lastname": "Hall" }, { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Bender" }, { "affiliation": "", "forename": "R E", "identifier": "", "initials": "RE", "lastname": "Marquis" } ]
1987-09
3305838
D000190:Actinomyces / Q000187:drug effects; D000900:Anti-Bacterial Agents; D001419:Bacteria / Q000187:drug effects*; D001441:Bacteroides fragilis / Q000187:drug effects; D003470:Culture Media; D004563:Electrochemistry; D004567:Electrodes, Implanted; D004926:Escherichia coli / Q000187:drug effects; D012834:Silver / Q000494:pharmacology* / Q000633:toxicity; D013211:Staphylococcus aureus / Q000187:drug effects; D013997:Time Factors; D014678:Veillonella / Q000187:drug effects
D016428:Journal Article
D000900:Anti-Bacterial Agents; D003470:Culture Media; D012834:Silver
10.1016/0278-2391(87)90202-3
[]
false
eng
J Oral Maxillofac Surg
8206428
0278-2391
United States
[]
"2024-08-13T08:46:10.083232Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The Registry of the International Society for Heart Transplantation: fourth official report--1987.
6(2)
63-7
The Journal of heart transplantation
[ { "affiliation": "", "forename": "M P", "identifier": "", "initials": "MP", "lastname": "Kaye" } ]
1987
3305830
D000293:Adolescent; D000328:Adult; D002648:Child; D002675:Child, Preschool; D016027:Heart Transplantation; D006801:Humans; D007166:Immunosuppressive Agents / Q000627:therapeutic use; D007223:Infant; D007231:Infant, Newborn; D007256:Information Systems; D007391:International Cooperation; D008875:Middle Aged; D012042:Registries; D012955:Societies, Medical; D013530:Surgical Wound Infection / Q000401:mortality; D013997:Time Factors; D014481:United States
D016428:Journal Article
D007166:Immunosuppressive Agents
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.084311Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Antithymocyte gamma globulin, low-dosage cyclosporine, and tapering steroids as an immunosuppressive regimen to avoid early kidney failure in heart transplantation.
6(2)
79-83
Cyclosporine is a powerful immunosuppressive agent that unfortunately has significant renal toxicity. Two risk factors associated with a high incidence of kidney failure in patients receiving cyclosporine have been described in the literature. In an effort to decrease the possibility of renal toxicity with the use of cyclosporine, we use low-dosage cyclosporine, antithymocyte gamma globulin, and tapering dosages of steroids as an immunosuppressive regimen. Twenty-one patients had orthotopic heart transplants from January 1985 to January 1986. Sixteen of 21 patients or 70% had at least one high risk factor for kidney failure. There were no episodes of acute kidney failure, and the blood urea nitrogen and creatinine levels that were recorded over an average of 8.5 months per patient did not increase significantly from preoperative values. Seventeen of 21 or 81% of the patients are alive and functioning fully. The incidence of rejection per patient was 0.9, and there were no biopsy-proven severe rejections. One patient died at 5 months; the autopsy showed generalized moderate rejection. There were 0.24 episodes of infection per patient, with one patient who died from Pneumocystis pneumonia. With this immunosuppression protocol, early postoperative kidney dysfunction was avoided. The incidences of rejection and infection were within acceptable range, and the quality of life in the 17 survivors is excellent.
The Journal of heart transplantation
[ { "affiliation": "", "forename": "G M", "identifier": "", "initials": "GM", "lastname": "Deeb" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Kolff" }, { "affiliation": "", "forename": "J B", "identifier": "", "initials": "JB", "lastname": "McClurken" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Dunn" }, { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Balsara" }, { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Ochs" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Badellino" }, { "affiliation": "", "forename": "T", "identifier": "", "initials": "T", "lastname": "Hollander" }, { "affiliation": "", "forename": "C", "identifier": "", "initials": "C", "lastname": "Eldridge" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Clancey" } ]
1987
3305833
D058186:Acute Kidney Injury / Q000517:prevention & control*; D000293:Adolescent; D000328:Adult; D000961:Antilymphocyte Serum / Q000627:therapeutic use*; D001806:Blood Urea Nitrogen; D002648:Child; D002675:Child, Preschool; D003404:Creatinine / Q000097:blood; D003524:Cyclosporins / Q000008:administration & dosage* / Q000097:blood / Q000627:therapeutic use; D004334:Drug Administration Schedule; D005260:Female; D006084:Graft Rejection; D016027:Heart Transplantation; D006801:Humans; D007165:Immunosuppression Therapy; D008297:Male; D008875:Middle Aged; D011183:Postoperative Complications; D013256:Steroids / Q000008:administration & dosage*; D013601:T-Lymphocytes / Q000276:immunology
D016428:Journal Article
D000961:Antilymphocyte Serum; D003524:Cyclosporins; D013256:Steroids; D003404:Creatinine
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.085408Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Painless swelling of the anterior maxillary gingiva.
45(9)
785-8
Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons
[ { "affiliation": "", "forename": "A R", "identifier": "", "initials": "AR", "lastname": "Gould" }, { "affiliation": "", "forename": "B", "identifier": "", "initials": "B", "lastname": "Alpert" } ]
1987-09
3305839
D000328:Adult; D003937:Diagnosis, Differential; D005260:Female; D005887:Gingival Neoplasms / Q000473:pathology*; D006801:Humans; D008223:Lymphoma / Q000473:pathology; D016403:Lymphoma, Large B-Cell, Diffuse / Q000473:pathology; D008228:Lymphoma, Non-Hodgkin / Q000473:pathology*; D009808:Odontogenic Tumors / Q000473:pathology
D002363:Case Reports; D016428:Journal Article
10.1016/0278-2391(87)90203-5
[]
false
eng
J Oral Maxillofac Surg
8206428
0278-2391
United States
[]
"2024-08-13T08:46:10.086382Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Resistance to horizontal forces of dowel and amalgam-core restorations: a comparative study.
14(4)
337-44
Four designs of amalgam-core anchorage were compared in a laboratory study for the inability to withstand the horizontal component of occlusal force. Amalgam cores were constructed for extracted teeth with either composite resin-cemented Dentatus dowels, or with Para-post or Flexi-post dowels cemented with phosphate cement. All the posts were of comparable length and diameter. These anchorage designs were compared with each other and to a self-threading (TMS) pin-retained amalgam core, by application of horizontal force and recording forces causing failure. Flexi-post-retained amalgam cores failed at a mean force of 36.5 (+/- 8.5) kg while Dentatus-retained and Para-post-retained cores failed at 41.7 (+/- 8.0) kg and 46.6 (+/- 11.4) kg, respectively. TMS-retained cores resisted forces up to a mean force of 53.5 (+/- 4.5) kg. Patterns of failure varied widely among these groups. Composite resin-cemented Dentatus dowels were retained in the tooth in nine out of ten samples, while none of the ten Flexi-post dowels and only one of the ten Para-post dowels did so. Tooth fracture on failure occurred in seven out of ten Flexi-post-retained cores, while only three out of ten of the Para-post-retained cores and none of the Dentatus dowel-retained cores presented this unrepairable type of failure. Possible reasons for these differences are discussed.
Journal of oral rehabilitation
[ { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Gordon" }, { "affiliation": "", "forename": "Z", "identifier": "", "initials": "Z", "lastname": "Metzger" } ]
1987-07
3305840
D001732:Bite Force; D003442:Crowns; D003723:Dental Amalgam; D003766:Dental Occlusion; D003779:Denture Design; D003781:Denture Retention; D004868:Equipment Failure; D006801:Humans; D011176:Post and Core Technique; D013314:Stress, Mechanical
D003160:Comparative Study; D016428:Journal Article
D003723:Dental Amalgam
10.1111/j.1365-2842.1987.tb00727.x
[]
false
eng
J Oral Rehabil
0433604
0305-182X
England
[]
"2024-08-13T08:46:10.088223Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Treatment times for adhesive bridges.
14(4)
371-7
The aim of this study was to collect information about the mean working time needed to accomplish the clinical procedures in applying an adhesive bridge, and to gain an insight into the factors that influence the working time. The study was carried out as part of a clinical trial. One hundred and fifty-one patients needing one adhesive bridge were selected for this study and divided between five operators. Clinical procedures were carried out following a written protocol. The statistical method consisted of an ANOVA after log-transformation of the working times. The total mean working time needed to accomplish the clinical procedures for adhesive bridges was 60.7 min (s.d. +/- 16.5 min). The mean working time increased by 30% where the abutment teeth were restored with class II or class III restorations. No influence was found related to: type of bridge (i.e. macromechanical versus micromechanical), type of luting resin and location of the bridge. A significant effect on the working times was found for: operator, tooth preparation and occlusal adjustments. With increasing experience of the operator the median working time decreased by up to 35%. The data from this study are considered as useful basic information for efficient planning in the dental practice and for a further cost-benefit analysis.
Journal of oral rehabilitation
[ { "affiliation": "", "forename": "N H", "identifier": "", "initials": "NH", "lastname": "Creugers" }, { "affiliation": "", "forename": "M A", "identifier": "", "initials": "MA", "lastname": "van't Hof" } ]
1987-07
3305841
D001840:Dental Bonding / Q000379:methods*; D003737:Dental Cavity Preparation / Q000379:methods*; D003767:Dental Occlusion, Balanced; D003779:Denture Design; D003830:Denture, Partial, Fixed; D006801:Humans; D013997:Time Factors
D016428:Journal Article
10.1111/j.1365-2842.1987.tb00731.x
[]
false
eng
J Oral Rehabil
0433604
0305-182X
England
[]
"2024-08-13T08:46:10.088994Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A study of the occlusal plane orientation in complete denture construction.
14(4)
399-404
A cephalometric study was conducted on eighteen dentulous subjects and fifty-six complete denture wearers to determine the location of the natural and artificial occlusal planes as related to Camper's plane. The results indicated that both the natural and artificial occlusal planes were not parallel to Camper's plane. However, the final anteroposterior inclination of the artificial occlusal plane in complete dentures was almost the same as the inclination of the natural occlusal plane.
Journal of oral rehabilitation
[ { "affiliation": "", "forename": "H C", "identifier": "", "initials": "HC", "lastname": "Karkazis" }, { "affiliation": "", "forename": "G L", "identifier": "", "initials": "GL", "lastname": "Polyzois" } ]
1987-07
3305842
D002508:Cephalometry / Q000379:methods*; D003766:Dental Occlusion; D003779:Denture Design; D003824:Denture, Complete; D005260:Female; D006801:Humans; D007575:Jaw, Edentulous / Q000473:pathology; D008297:Male
D003160:Comparative Study; D016428:Journal Article
10.1111/j.1365-2842.1987.tb00735.x
[]
false
eng
J Oral Rehabil
0433604
0305-182X
England
[]
"2024-08-13T08:46:10.089747Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Experimental vascularized bone grafts: histopathologic correlations with postoperative bone scan: the risk of false-positive results.
5(3)
311-9
A positive bone scan in an experimental model of bilateral ulna diaphyseal bone grafts demonstrated early bone repair in both vascularized and nonvascularized orthotopic ulna autografts. A positive bone scan did not correlate with the perfusion of the vascularized and nonvascularized grafts as measured by microangiograms done 1 week postoperatively. In this model, if the bone scan is intended to monitor the circulatory status and viability of the bone graft, it must be done earlier than 1 week postoperative prior to the onset of creeping repair in both vascularized and nonvascular ulna autografts.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society
[ { "affiliation": "", "forename": "J W", "identifier": "", "initials": "JW", "lastname": "Shaffer" }, { "affiliation": "", "forename": "G A", "identifier": "", "initials": "GA", "lastname": "Field" }, { "affiliation": "", "forename": "R G", "identifier": "", "initials": "RG", "lastname": "Wilber" }, { "affiliation": "", "forename": "V M", "identifier": "", "initials": "VM", "lastname": "Goldberg" } ]
1987
3305843
D000818:Animals; D016025:Bone Transplantation; D001842:Bone and Bones / Q000000981:diagnostic imaging / Q000473:pathology; D004285:Dogs; D005189:False Positive Reactions; D006652:Histological Techniques; D008852:Microradiography; D011184:Postoperative Period; D011877:Radionuclide Imaging; D014182:Transplantation, Autologous; D014457:Ulna / Q000637:transplantation
D003160:Comparative Study; D016428:Journal Article; D013486:Research Support, U.S. Gov't, Non-P.H.S.
10.1002/jor.1100050302
[]
false
eng
J Orthop Res
8404726
0736-0266
United States
[]
"2024-08-13T08:46:10.090662Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The effect of proximally and fully porous-coated canine hip stem design on bone modeling.
5(3)
393-408
Porous coated canine femoral hip replacement implants were evaluated for biological fixation by bone ingrowth and the effect of the extent of porous coating on bone modeling. The Co-Cr alloy implants were either fully porous coated or coated only on the proximal 40% of the stem. Two implants of each type were studied 9, 16, and 36 months after surgery. Implant fixation and bone modeling were assessed radiographically throughout the implant periods and histologically after the test animals were killed. All 12 implants appeared stably fixed within the femur and were bone-ingrown in the porous region. Radiographic features such as proximal medial and anterior cortical thinning, proximal cancellous bone hypertrophy, and new endosteal bone formation near the stem tip were noted within the first postoperative year, with no appreciable change thereafter. The extent of proximal cortical thinning varied from virtually none to as much as 40%, being more prominent with the proximally coated implants at 16 months and with the fully coated implants at 36 months. Of consistent note was cancellous hypertrophy at the junction of porous and smooth implant surfaces with proximally coated implants and new endosteal bone formation and ingrowth at the stem tip of fully coated implants. These results indicate that the proximally porous-coated implant design causes increased proximal stress transfer, but this does not necessarily preclude proximal cortical resorption.
Journal of orthopaedic research : official publication of the Orthopaedic Research Society
[ { "affiliation": "", "forename": "J D", "identifier": "", "initials": "JD", "lastname": "Bobyn" }, { "affiliation": "", "forename": "R M", "identifier": "", "initials": "RM", "lastname": "Pilliar" }, { "affiliation": "", "forename": "A G", "identifier": "", "initials": "AG", "lastname": "Binnington" }, { "affiliation": "", "forename": "J A", "identifier": "", "initials": "JA", "lastname": "Szivek" } ]
1987
3305844
D000222:Adaptation, Physiological; D000818:Animals; D004285:Dogs; D005269:Femur / Q000033:anatomy & histology / Q000000981:diagnostic imaging / Q000502:physiology*; D005500:Follow-Up Studies; D006622:Hip Prosthesis / Q000009:adverse effects; D006652:Histological Techniques; D011859:Radiography; D012107:Research Design; D013997:Time Factors
D003160:Comparative Study; D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
10.1002/jor.1100050312
[]
false
eng
87310882
J Orthop Res
8404726
0736-0266
United States
[]
"2024-08-13T08:46:10.091504Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Use of the monoclonal antibody WR17, identifying the CD37 gp40-45 Kd antigen complex, in the diagnosis of B-lymphoid malignancy.
152(1)
13-21
The distribution of the gp40-45 Kd antigen bound by the WR17 monoclonal antibody of IgG2 subclass in normal lymphoid tissue was characterized by immunohistochemistry and immunofluorescence staining with flow cytometric analysis. The predominant staining pattern observed was characteristic of an anti-pan-B-lymphocyte reagent. Weak reactions were observed by immunofluorescence staining of viable cell suspensions with all neutrophils and T-lymphocytes in some normal donors. In tissue sections, B-lymphocytes were stained and no cross reactions were observed with T-lymphocytes, although macrophages stained in some sections. A range of T- and B-cell malignancies were stained with WR17 and the reactivity compared to that observed with other monoclonal antibodies in the CD19, CD21 and CD22 clusters. All B-non-Hodgkin's lymphomas, B-chronic lymphocytic, prolymphocytic and hairy cell leukaemia cells examined were stained by WR17 in indirect immunofluorescence assays, whilst the T-cell tumours were negative. The same pattern was observed in cryostat sections of malignant tissue and in addition some tissue macrophages expressed the CD37 antigen cytoplasmically. Intra-tumour heterogeneity of staining was observed with all the monoclonal antibodies tested, although overall WR17 consistently stained B-cell tumours even when expression of the CD19 pan-B-lymphocyte antigen could not be detected with some monoclonals. Monoclonal antibodies, such as WR17, within the CD37 cluster and binding to the gp 40-45 Kd molecule, bind to mature B-lymphocytes and identify the majority of B-cell malignancies.
The Journal of pathology
[ { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Moore" }, { "affiliation": "", "forename": "S A", "identifier": "", "initials": "SA", "lastname": "Cooper" }, { "affiliation": "", "forename": "D B", "identifier": "", "initials": "DB", "lastname": "Jones" } ]
1987-05
3305845
D000911:Antibodies, Monoclonal; D001402:B-Lymphocytes / Q000276:immunology*; D005455:Fluorescent Antibody Technique; D006801:Humans; D007124:Immunoenzyme Techniques; D007938:Leukemia / Q000175:diagnosis*; D007943:Leukemia, Hairy Cell / Q000175:diagnosis; D007945:Leukemia, Lymphoid / Q000175:diagnosis; D008228:Lymphoma, Non-Hodgkin / Q000175:diagnosis*
D016428:Journal Article
D000911:Antibodies, Monoclonal
10.1002/path.1711520103
[]
false
eng
J Pathol
0204634
0022-3417
England
[]
"2024-08-13T08:46:10.093487Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Early, aggressive open lung biopsy in heart transplant recipients.
6(2)
96-9
Fourteen open lung biopsies were done in 13 patients out of a total of 63 heart transplant recipients. All of the patients were receiving cyclosporine and azathioprine (Imuran) and had received prophylactic antithymocyte globulin or murine antihuman mature T cell (OKT3). Eight of the patients were receiving steroids, and five of the patients had been weaned off steroids. A fever of greater than 38.5 degrees C was present in all 13 patients. Hypoxia, defined as PO2 less than 60 on room air, was present in 11 of the 13 patients. One patient had to be intubated before surgery for respiratory failure. The chest x-ray film most often revealed bilateral interstitial infiltrates. The operative approach was by a small anterior thoracotomy in 12 patients and a posterolateral thoracotomy in two patients. A definitive diagnosis was made in 11 of the 14 open lung biopsies: three patients had Legionella, one had cytomegalovirus (CMV), one had a Pseudomonas infection, three had Pneumocystis, one patient had CMV and Pneumocystis, one patient had a pulmonary infarct, and one patient had a pulmonary infarct and CMV. Specific therapy was instituted in all these patients. In the three patients in whom no specific diagnosis was made, therapy was also changed and the use of antibiotics discontinued. There was no mortality in this group. Morbidity was minimal. No patient had excessive bleeding, and none of the patients required the transfusion of blood or blood products. Three patients required mechanical ventilatory support for longer than 24 hours.(ABSTRACT TRUNCATED AT 250 WORDS)
The Journal of heart transplantation
[ { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Miller" }, { "affiliation": "", "forename": "N A", "identifier": "", "initials": "NA", "lastname": "Burton" }, { "affiliation": "", "forename": "S V", "identifier": "", "initials": "SV", "lastname": "Karwande" }, { "affiliation": "", "forename": "K W", "identifier": "", "initials": "KW", "lastname": "Jones" }, { "affiliation": "", "forename": "D B", "identifier": "", "initials": "DB", "lastname": "Doty" }, { "affiliation": "", "forename": "W A", "identifier": "", "initials": "WA", "lastname": "Gay" } ]
1987
3305835
D000328:Adult; D001706:Biopsy / Q000379:methods*; D005260:Female; D016027:Heart Transplantation; D006801:Humans; D007165:Immunosuppression Therapy; D008168:Lung / Q000473:pathology*; D008171:Lung Diseases / Q000175:diagnosis* / Q000000981:diagnostic imaging; D008297:Male; D008875:Middle Aged; D009894:Opportunistic Infections / Q000175:diagnosis* / Q000000981:diagnostic imaging; D013902:Radiography, Thoracic
D016428:Journal Article
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.094422Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Use of cyclosporine and ketoconazole without nephrotoxicity in two heart transplant recipients.
6(2)
84-9
A cyclosporine-ketoconazole drug interaction was first described in 1981. It has been suggested that the two drugs should not be used concomitantly because of the danger of severe nephrotoxicity. Two reported cases indicate that cyclosporine and ketoconazole can be safely coadministered, provided that the dosage of cyclosporine is reduced appropriately. Two patients were initially given 8 mg/kg/day of cyclosporine at the time of heart transplantation, and the dosage was tapered to meet appropriate blood levels (250 to 350 ng/ml by whole blood high-performance liquid chromatography). During ketoconazole therapy (400 mg daily for 4 weeks), patient 1 received 80 to 100 mg/day of cyclosporine, which is equal to approximately 1 mg/kg/day, and patient 2 received between 40 and 80 mg/day of cyclosporine, which is equivalent to 0.4 to 0.8 mg/kg/day. Neither patient exhibited a creatinine value above 1.4 mg/dl while on combined therapy, and there were no problems with allograft rejection. Both patients had inappropriately high cyclosporine blood levels even with this marked reduction in dosage (patient 1, 520 to 1310 ng/ml and patient 2, 320 to 600 ng/ml). Thus it appears that cyclosporine and ketoconazole can be administered together safely, provided that there is an appropriate reduction in the dosage of cyclosporine; this results in the maintenance of adequate immunosuppression without development of nephrotoxicity.
The Journal of heart transplantation
[ { "affiliation": "", "forename": "T J", "identifier": "", "initials": "TJ", "lastname": "Schroeder" }, { "affiliation": "", "forename": "D B", "identifier": "", "initials": "DB", "lastname": "Melvin" }, { "affiliation": "", "forename": "C W", "identifier": "", "initials": "CW", "lastname": "Clardy" }, { "affiliation": "", "forename": "N K", "identifier": "", "initials": "NK", "lastname": "Wadhwa" }, { "affiliation": "", "forename": "S A", "identifier": "", "initials": "SA", "lastname": "Myre" }, { "affiliation": "", "forename": "J M", "identifier": "", "initials": "JM", "lastname": "Reising" }, { "affiliation": "", "forename": "R K", "identifier": "", "initials": "RK", "lastname": "Wolf" }, { "affiliation": "", "forename": "J A", "identifier": "", "initials": "JA", "lastname": "Collins" }, { "affiliation": "", "forename": "A J", "identifier": "", "initials": "AJ", "lastname": "Pesce" }, { "affiliation": "", "forename": "M R", "identifier": "", "initials": "MR", "lastname": "First" } ]
1987
3305834
D003524:Cyclosporins / Q000627:therapeutic use*; D004359:Drug Therapy, Combination; D016027:Heart Transplantation; D006801:Humans; D007654:Ketoconazole / Q000627:therapeutic use*; D007668:Kidney / Q000187:drug effects*; D008297:Male; D008875:Middle Aged
D002363:Case Reports; D016428:Journal Article
D003524:Cyclosporins; D007654:Ketoconazole
[]
false
eng
J Heart Transplant
8604172
0887-2570
United States
[]
"2024-08-13T08:46:10.095483Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Pathogenicity of HIV in lymphatic organs of patients with AIDS.
152(1)
31-5
HIV antigens were searched for in the thymus, lymph nodes, bone marrow, and spleen of AIDS patients, by means of immunofluorescence technique. Human IgG against HIV and monoclonal antibodies against viral gag P24 protein yielded strong cytoplasmic fluorescence of cells in sections of the thymus, lymph nodes and spleen. Some cells containing HIV antigens were morphologically multinucleated giant cells. They reacted with monoclonal antibodies against helper/inducer T-cells (OKT4+), and were complexed with antibody or with complement as demonstrated by double-staining immunofluorescence technique. A large number of inflammatory cells infiltrated the thymus in areas containing cells expressing HIV antigens. These studies demonstrated an association of HIV virus with cytopathic and immunopathogenic reactions in lymphatic organs of AIDS patients, and are consistent with previous results, as well as indicative of a primary aetiologic role for the virus.
The Journal of pathology
[ { "affiliation": "", "forename": "D D", "identifier": "", "initials": "DD", "lastname": "Pekovic" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Gornitsky" }, { "affiliation": "", "forename": "D", "identifier": "", "initials": "D", "lastname": "Ajdukovic" }, { "affiliation": "", "forename": "J M", "identifier": "", "initials": "JM", "lastname": "Dupuy" }, { "affiliation": "", "forename": "J P", "identifier": "", "initials": "JP", "lastname": "Chausseau" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Michaud" }, { "affiliation": "", "forename": "N", "identifier": "", "initials": "N", "lastname": "Lapointe" }, { "affiliation": "", "forename": "N", "identifier": "", "initials": "N", "lastname": "Gilmore" }, { "affiliation": "", "forename": "C", "identifier": "", "initials": "C", "lastname": "Tsoukas" }, { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Zwadlo" } ]
1987-05
3305846
D000163:Acquired Immunodeficiency Syndrome / Q000276:immunology* / Q000473:pathology; D000914:Antibodies, Viral / Q000032:analysis*; D000956:Antigens, Viral / Q000032:analysis; D001853:Bone Marrow / Q000276:immunology; D005455:Fluorescent Antibody Technique; D006678:HIV / Q000276:immunology*; D006801:Humans; D007074:Immunoglobulin G / Q000032:analysis; D008221:Lymphoid Tissue / Q000276:immunology* / Q000473:pathology
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
D000914:Antibodies, Viral; D000956:Antigens, Viral; D007074:Immunoglobulin G
10.1002/path.1711520105
[]
false
eng
J Pathol
0204634
0022-3417
England
[]
"2024-08-13T08:46:10.096732Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Endotoxin induced hepatic necrosis in rats on an alcohol diet.
152(1)
47-53
The role of endotoxin in the pathogenesis of progressive liver disease is receiving increasing attention, but remains controversial. Similarly, although alcoholic hepatitis is now recognized as the transitional link between alcoholic fatty liver and advanced alcoholic liver disease, the aetiology of liver cell necrosis in alcoholic hepatitis is not known. Rats fed a nutritionally adequate liquid alcohol diet according to the formula of Lieber and DeCarli developed fatty livers. Littermates fed an identical diet and challenged with small IV doses (1 microgram/g body weight) of E. coli lipopolysaccharide endotoxin (LPS) developed focal necrotizing hepatitis. Control littermates fed an identical calorie balanced but alcohol free diet and challenged with identical doses of LPS did not develop any liver lesions. The hepatocyte necrosis with associated inflammatory changes induced by LPS in fatty livers has some features of early human alcoholic hepatitis and suggests that progressive alcohol induced damage may be multifactorial in origin.
The Journal of pathology
[ { "affiliation": "", "forename": "B S", "identifier": "", "initials": "BS", "lastname": "Bhagwandeen" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Apte" }, { "affiliation": "", "forename": "L", "identifier": "", "initials": "L", "lastname": "Manwarring" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Dickeson" } ]
1987-05
3305847
D000818:Animals; D001219:Aspartate Aminotransferases / Q000378:metabolism; D056486:Chemical and Drug Induced Liver Injury / Q000209:etiology; D004032:Diet; D004357:Drug Synergism; D004731:Endotoxins / Q000633:toxicity*; D004926:Escherichia coli; D000431:Ethanol / Q000008:administration & dosage / Q000633:toxicity*; D005235:Fatty Liver, Alcoholic / Q000209:etiology; D006519:Hepatitis, Alcoholic / Q000209:etiology; D008070:Lipopolysaccharides / Q000633:toxicity*; D008099:Liver / Q000201:enzymology / Q000473:pathology; D008107:Liver Diseases / Q000209:etiology* / Q000473:pathology; D008297:Male; D009336:Necrosis; D009504:Neutrophils; D051381:Rats; D011919:Rats, Inbred Strains
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
D004731:Endotoxins; D008070:Lipopolysaccharides; D000431:Ethanol; D001219:Aspartate Aminotransferases
10.1002/path.1711520107
[]
false
eng
J Pathol
0204634
0022-3417
England
[]
"2024-08-13T08:46:10.097948Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Cerebral ventricular dilation in congenital myotonic dystrophy.
111(3)
372-6
Ultrasonography or computed tomography scanning of the brain was performed in 10 infants with congenital myotonic dystrophy between the age of 1 day and 2 months, and showed intracranial abnormalities in all. Ventricular dilation was diagnosed in eight (80%), subarachnoid hemorrhage in one, and white matter infarcts in one. The common finding of ventricular dilation is probably related to developmental brain abnormality dating back to fetal life, because it was already present in three infants scanned on the first day of life. Neonatal asphyxia was present in seven infants, associated with intraventricular hemorrhage in two. The relationship between these changes and mental retardation, which is a common feature in this disease, is unclear.
The Journal of pediatrics
[ { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Regev" }, { "affiliation": "", "forename": "L S", "identifier": "", "initials": "LS", "lastname": "de Vries" }, { "affiliation": "", "forename": "J Z", "identifier": "", "initials": "JZ", "lastname": "Heckmatt" }, { "affiliation": "", "forename": "V", "identifier": "", "initials": "V", "lastname": "Dubowitz" } ]
1987-09
3305848
D002552:Cerebral Ventricles / Q000002:abnormalities*; D004108:Dilatation, Pathologic / Q000473:pathology; D006801:Humans; D007223:Infant; D007231:Infant, Newborn; D009223:Myotonic Dystrophy / Q000151:congenital* / Q000473:pathology; D013345:Subarachnoid Hemorrhage / Q000473:pathology; D014057:Tomography, X-Ray Computed; D014463:Ultrasonography
D016428:Journal Article
10.1016/s0022-3476(87)80456-0
[]
false
eng
J Pediatr
0375410
0022-3476
United States
[]
"2024-08-13T08:46:10.099913Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Association of supernumerary nipples with renal anomalies.
111(3)
412-3
The Journal of pediatrics
[ { "affiliation": "", "forename": "V", "identifier": "", "initials": "V", "lastname": "Meggyessy" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Méhes" } ]
1987-09
3305849
D000015:Abnormalities, Multiple / Q000175:diagnosis*; D001940:Breast / Q000002:abnormalities*; D002648:Child; D005260:Female; D006801:Humans; D007668:Kidney / Q000002:abnormalities*; D008297:Male; D009558:Nipples / Q000002:abnormalities*; D014463:Ultrasonography
D016428:Journal Article
10.1016/s0022-3476(87)80468-7
[]
false
eng
J Pediatr
0375410
0022-3476
United States
[]
"2024-08-13T08:46:10.100679Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Oral theophylline and diuretics improve pulmonary mechanics in infants with bronchopulmonary dysplasia.
111(3)
439-44
We studied the effects of orally administered theophylline and diuretics (chlorothiazide and spironolactone) on pulmonary mechanics in 16 infants with bronchopulmonary dysplasia. Their gestational age (mean +/- SD) was 28.5 +/- 3.4 weeks, and postnatal age at the time of study 19.5 +/- 10.7 weeks. The infants were randomized to two groups. Group 1 received successively placebo, theophylline, and theophylline plus diuretics; Group 2 received theophylline, placebo, and placebo plus diuretics on successive 4-day periods. Pulmonary function was measured before beginning the study (baseline) and at the end of each 4-day period. No significant changes in pulmonary function were noted after treatment with placebo. After treatment with theophylline, dynamic compliance (Cdyn) increased from baseline (mean +/- SD) 0.075 +/- 0.017 to 0.091 +/- 0.028 mL/cm H2O/cm (P less than 0.01), airway resistance (Raw) decreased from 67.19 +/- 36.71 to 41.44 +/- 22.50 cm H2O/L/sec (P less than 0.001), maximal expiratory flow at functional residual capacity (VmaxFRC) increased from 0.261 +/- 0.240 to 0.357 +/- 0.299 thoracic gas volume (TGV)/sec (P less than 0.01), and time constant decreased from 0.312 +/- 0.224 to 0.275 +/- 0.247 sec (P less than 0.02). After treatment with combined placebo and diuretics, Cdyn increased to 0.103 +/- 0.023 mL/cm H2O/cm (P less than 0.05), Raw decreased to 31.76 +/- 24.90 cm H2O/L/sec (P less than 0.001), VmaxFRC increased to 0.638 +/- 0.595 TGV/sec (P less than 0.02), and time constant decreased to 0.180 +/- 0.141 sec (P less than 0.05). After treatment with combined theophylline and diuretics, Cdyn increased to 0.118 +/- 0.017 mL/cm H2O/cm (P less than 0.001), Raw decreased to 35.98 +/- 25.85 cm H2O/L/sec (P less than 0.02), VmaxFRC increased to 0.479 +/- 0.377 TGV/sec (P less than 0.02), and time constant decreased to 0.180 +/- 0.137 sec (P less than 0.01). We conclude that theophylline and diuretics have additive effects on the improvement of pulmonary function in infants with bronchopulmonary dysplasia.
The Journal of pediatrics
[ { "affiliation": "", "forename": "L C", "identifier": "", "initials": "LC", "lastname": "Kao" }, { "affiliation": "", "forename": "D J", "identifier": "", "initials": "DJ", "lastname": "Durand" }, { "affiliation": "", "forename": "B L", "identifier": "", "initials": "BL", "lastname": "Phillips" }, { "affiliation": "", "forename": "B G", "identifier": "", "initials": "BG", "lastname": "Nickerson" } ]
1987-09
3305850
D000284:Administration, Oral; D001997:Bronchopulmonary Dysplasia / Q000188:drug therapy*; D002740:Chlorothiazide / Q000627:therapeutic use*; D002986:Clinical Trials as Topic; D004311:Double-Blind Method; D004359:Drug Therapy, Combination; D006801:Humans; D007223:Infant; D007231:Infant, Newborn; D008168:Lung / Q000187:drug effects*; D008176:Lung Volume Measurements; D012123:Pulmonary Ventilation / Q000187:drug effects; D011897:Random Allocation; D013148:Spironolactone / Q000627:therapeutic use*; D013806:Theophylline / Q000627:therapeutic use*
D016430:Clinical Trial; D003160:Comparative Study; D016428:Journal Article; D016449:Randomized Controlled Trial; D013485:Research Support, Non-U.S. Gov't
D013148:Spironolactone; D002740:Chlorothiazide; D013806:Theophylline
10.1016/s0022-3476(87)80476-6
[]
false
eng
J Pediatr
0375410
0022-3476
United States
[]
"2024-08-13T08:46:10.101724Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Effects of theophylline on learning and behavior: reason for concern or concern without reason?
111(3)
471-4
The Journal of pediatrics
[ { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Weinberger" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Lindgren" }, { "affiliation": "", "forename": "B", "identifier": "", "initials": "B", "lastname": "Bender" }, { "affiliation": "", "forename": "J A", "identifier": "", "initials": "JA", "lastname": "Lerner" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Szefler" } ]
1987-09
3305851
D001249:Asthma / Q000188:drug therapy*; D002648:Child; D002652:Child Behavior / Q000187:drug effects*; D002653:Child Behavior Disorders / Q000139:chemically induced; D003863:Depression / Q000139:chemically induced; D006801:Humans; D007858:Learning / Q000187:drug effects*; D007859:Learning Disabilities / Q000139:chemically induced; D013806:Theophylline / Q000009:adverse effects* / Q000627:therapeutic use
D016428:Journal Article; D016454:Review
D013806:Theophylline
10.1016/s0022-3476(87)80483-3
[]
false
eng
J Pediatr
0375410
0022-3476
United States
[]
"2024-08-13T08:46:10.102757Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Macrophage function in patients with American cutaneous leishmaniasis: in vitro cytotoxicity and interleukin-1 production.
73(4)
769-73
Monocyte-derived blood macrophages of untreated patients with Leishmania braziliensis or Leishmania mexicana amazonensis infections show anomalies in their nonspecific immune functions. Their ability to kill HeLa cells or to produce interleukin-1 in vitro in response to lipopolysaccharide plus Candida albicans is lower than controls indicating that acquired or innate macrophage deficiencies may be involved in the course of the disease.
The Journal of parasitology
[ { "affiliation": "", "forename": "P R", "identifier": "", "initials": "PR", "lastname": "Ridel" }, { "affiliation": "", "forename": "J P", "identifier": "", "initials": "JP", "lastname": "Dedet" }, { "affiliation": "", "forename": "P", "identifier": "", "initials": "P", "lastname": "Esterre" } ]
1987-08
3305852
D000293:Adolescent; D000328:Adult; D002176:Candida albicans / Q000276:immunology; D003602:Cytotoxicity, Immunologic; D015232:Dinoprostone; D006367:HeLa Cells; D006801:Humans; D007375:Interleukin-1 / Q000096:biosynthesis*; D007892:Leishmania braziliensis; D007894:Leishmania mexicana; D007896:Leishmaniasis / Q000276:immunology*; D008070:Lipopolysaccharides / Q000276:immunology; D008213:Lymphocyte Activation; D008264:Macrophages / Q000276:immunology*; D011458:Prostaglandins E / Q000096:biosynthesis; D013601:T-Lymphocytes / Q000276:immunology
D016428:Journal Article
D007375:Interleukin-1; D008070:Lipopolysaccharides; D011458:Prostaglandins E; D015232:Dinoprostone
[]
false
eng
J Parasitol
7803124
0022-3395
United States
[]
"2024-08-13T08:46:10.103747Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Cyclosporin-A-induced gingival enlargement. A case report.
58(7)
475-80
Cyclosporin-A (CsA)-induced gingival enlargement has been reported in a small number of cases but may involve up to one third of all patients taking CsA. The present study reports a case of CsA-induced gingival enlargement during suppressive therapy for myasthenia gravis. Gingival tissues were examined histologically, histochemically, and immunohistologically. The basic tissue response seemed to be a dental plaque- and trauma-induced fibroblastic response characterized by large aggregations of plasma cells, macrophages and helper T lymphocytes. The reactive areas rapidly matured into noninflamed fibrocytic tissue. The suppressive effect of CsA appears responsible for removal of sectors of the normal immune response and, in combination with an elevated number of macrophages, may be instrumental in initiating a fibrous hyperplastic response.
Journal of periodontology
[ { "affiliation": "", "forename": "N W", "identifier": "", "initials": "NW", "lastname": "Savage" }, { "affiliation": "", "forename": "G J", "identifier": "", "initials": "GJ", "lastname": "Seymour" }, { "affiliation": "", "forename": "M F", "identifier": "", "initials": "MF", "lastname": "Robinson" } ]
1987-07
3305854
D000328:Adult; D003524:Cyclosporins / Q000009:adverse effects*; D005881:Gingiva / Q000473:pathology; D005885:Gingival Hyperplasia / Q000139:chemically induced* / Q000473:pathology; D006651:Histocytochemistry; D006801:Humans; D007158:Immunologic Techniques; D008297:Male; D009157:Myasthenia Gravis / Q000188:drug therapy
D002363:Case Reports; D016428:Journal Article
D003524:Cyclosporins
10.1902/jop.1987.58.7.475
[]
false
eng
J Periodontol
8000345
0022-3492
United States
[]
"2024-08-13T08:46:10.105743Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A survey of Bancroftian filariasis in the Dominican Republic.
73(4)
839-40
The Journal of parasitology
[ { "affiliation": "", "forename": "A L", "identifier": "", "initials": "AL", "lastname": "Vincent" }, { "affiliation": "", "forename": "A", "identifier": "", "initials": "A", "lastname": "Gonzalvo" }, { "affiliation": "", "forename": "B C", "identifier": "", "initials": "BC", "lastname": "Cowell" }, { "affiliation": "", "forename": "J K", "identifier": "", "initials": "JK", "lastname": "Nayar" }, { "affiliation": "", "forename": "L", "identifier": "", "initials": "L", "lastname": "Uribe" } ]
1987-08
3305853
D000293:Adolescent; D000328:Adult; D000330:Aedes / Q000469:parasitology; D000368:Aged; D000818:Animals; D002648:Child; D003465:Culex / Q000469:parasitology; D004293:Dominican Republic; D004605:Elephantiasis, Filarial / Q000453:epidemiology*; D005260:Female; D006801:Humans; D007303:Insect Vectors / Q000469:parasitology; D008209:Lymphedema / Q000453:epidemiology*; D008297:Male; D008875:Middle Aged; D014958:Wuchereria bancrofti / Q000302:isolation & purification
D016428:Journal Article
[]
false
eng
J Parasitol
7803124
0022-3395
United States
[]
"2024-08-13T08:46:10.106696Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Ultrastructural and immunocytochemical characterization of polymorphonuclear leukocytes from gingival crevice in man.
58(7)
493-7
Polymorphonuclear leukocytes from the gingival crevicular fluid (CF-PMNs) of patients with generalized severe periodontitis were examined using electron microscopy and immunocytochemical techniques. CF-PMNs were found to contain numerous phagocytic vacuoles. This suggests that CF-PMNs actively phagocytized various substances from the environment. Immunocytochemical staining with FITC-conjugated IgG, IgM, and IgA reagents and TRITC-conjugated C3 reagent was applied to CF-PMNs as well as peripheral blood PMNs incubated with cell-free crevicular fluid. The cytoplasm of PMNs exhibited numerous granular foci of immunofluorescence. This finding suggests that these proteins were acquired from the environment by PMNs. The coincidental appearances of immunoglobulins and C3 in a single cell were considered to be immune complexes phagocytized by CF-PMNs in generalized severe periodontitis.
Journal of periodontology
[ { "affiliation": "", "forename": "I", "identifier": "", "initials": "I", "lastname": "Saito" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Komiyama" }, { "affiliation": "", "forename": "I", "identifier": "", "initials": "I", "lastname": "Moro" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Akachi" }, { "affiliation": "", "forename": "N", "identifier": "", "initials": "N", "lastname": "Shiomi" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Ito" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Murai" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Umemura" } ]
1987-07
3305855
D000328:Adult; D002452:Cell Count; D003165:Complement System Proteins / Q000032:analysis; D005883:Gingival Crevicular Fluid / Q000276:immunology*; D005891:Gingivitis / Q000276:immunology*; D006801:Humans; D007136:Immunoglobulins / Q000032:analysis*; D008875:Middle Aged; D009504:Neutrophils / Q000276:immunology / Q000648:ultrastructure*; D010518:Periodontitis / Q000276:immunology / Q000473:pathology*
D016428:Journal Article
D007136:Immunoglobulins; D003165:Complement System Proteins
10.1902/jop.1987.58.7.493
[]
false
eng
J Periodontol
8000345
0022-3492
United States
[]
"2024-08-13T08:46:10.107841Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Tissue localization of Actinobacillus actinomycetemcomitans in human periodontitis. I. Light, immunofluorescence and electron microscopic studies.
58(8)
529-39
Invasion of periodontal tissues by different bacterial morphotypes has been reported in human periodontitis; however, limited information is available as to prevalence, localization and the bacterial species involved. The present study determined prevalence and gingival localization of Actinobacillus (Haemophilus) actinomycetemcomitans in periodontal lesions of juvenile periodontitis patients. Thirty-five gingival biopsies were obtained from 12 juvenile periodontitis patients at the time of periodontal therapy. One additional control biopsy was obtained from each of two adult periodontally healthy subjects, one adult periodontitis patient and one periodontally healthy monkey (Macaca fosibolius). The biopsies were carefully processed to avoid mechanical introduction of bacteria into the tissues and were examined using light and electron microscopy. Rabbit antisera specific for the three A. actinomycetemcomitans serotypes were used for immunofluorescence microscopic localization of A. actinomycetemcomitans antigens in the gingival sections. Immunofluorescence microscopy showed A. actinomycetemcomitans specific antigens in the gingival tissues of 11 of the 12 juvenile patients examined. None of the control specimens showed evidence of A. actinomycetemcomitans antigens in the gingival connective tissue. One specimen from a periodontally healthy subject and the monkey biopsy, however, showed A. actinomycetemcomitans antigens in bacterial plaque on the surface of the crevicular epithelium. Transmission electron microscopic examination showed microcolonies of small gram-negative rods in the connective tissue, as well as single bacterial cells between collagen fibers and in areas of cell debris. In addition to these extracellular bacterial cells, evidence of bacterial cells was also found within gingival connective tissue phagocytic cells. The data from the present study suggest that the gingival tissue in juvenile periodontitis lesions harbors A. actinomycetemcomitans.
Journal of periodontology
[ { "affiliation": "", "forename": "L A", "identifier": "", "initials": "LA", "lastname": "Christersson" }, { "affiliation": "", "forename": "B", "identifier": "", "initials": "B", "lastname": "Albini" }, { "affiliation": "", "forename": "J J", "identifier": "", "initials": "JJ", "lastname": "Zambon" }, { "affiliation": "", "forename": "U M", "identifier": "", "initials": "UM", "lastname": "Wikesjö" }, { "affiliation": "", "forename": "R J", "identifier": "", "initials": "RJ", "lastname": "Genco" } ]
1987-08
3305856
D000188:Actinobacillus / Q000648:ultrastructure*; D000293:Adolescent; D000328:Adult; D010520:Aggressive Periodontitis / Q000382:microbiology* / Q000473:pathology / Q000628:therapy; D002648:Child; D003773:Dental Plaque / Q000382:microbiology; D005260:Female; D005455:Fluorescent Antibody Technique; D005881:Gingiva / Q000382:microbiology*; D006801:Humans; D008297:Male; D008875:Middle Aged; D010510:Periodontal Diseases / Q000382:microbiology*
D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S.
10.1902/jop.1987.58.8.529
[]
false
eng
J Periodontol
8000345
0022-3492
United States
[ { "agency": "NIDCR NIH HHS", "country": "United States", "grant_acronym": "DE", "grant_id": "DE04898" } ]
"2024-08-13T08:46:10.108790Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Tissue localization of Actinobacillus actinomycetemcomitans in human periodontitis. II. Correlation between immunofluorescence and culture techniques.
58(8)
540-5
Recent immunohistological studies have suggested that Actinobacillus actinomycetemcomitans is present in the gingival tissues in juvenile periodontitis lesions. The present study examined tissue bound A. actinomycetemcomitans by bacterial culture and immunohistological demonstration of antigen in tissue. A total of 14 periodontitis lesions were examined. Eleven biopsies were obtained from gingiva adjacent to A. actinomycetemcomitans infected pockets, while the remaining three control biopsies were obtained from gingiva adjacent to pockets where subgingival A. actinomycetemcomitans infection could not be detected. Each biopsy was hemisected, one half was used for immunofluorescence microscopic examination while the other half was processed for culture of A. actinomycetemcomitans. The latter section was surface-disinfected, repeatedly washed and then minced to release bacteria from within the tissues. Aliquots from the serial washings and the minced tissue suspension were cultured on medium selective for A. actinomycetemcomitans. Surface disinfection and serial washings gradually decreased cultivable A. actinomycetemcomitans in the washings aliquots. Following tissue disruption, an increase in colony-forming units of A. actinomycetemcomitans was seen from eight of the 11 test biopsies. This bacterium could not be detected in washings or minced tissue suspensions from the control biopsies obtained from lesions in which subgingival A. actinomycetemcomitans was previously not detected. A positive correlation was seen between the presence of A. actinomycetemcomitans antigens in the gingival biopsies and; (1) A. actinomycetemcomitans colony-forming units released from the minced tissues (r = 0.90, p = 0.000), as well as; (2) the colony-forming units from the periodontal pocket (r = 0.62, P = 0.017).(ABSTRACT TRUNCATED AT 250 WORDS)
Journal of periodontology
[ { "affiliation": "", "forename": "L A", "identifier": "", "initials": "LA", "lastname": "Christersson" }, { "affiliation": "", "forename": "U M", "identifier": "", "initials": "UM", "lastname": "Wikesjö" }, { "affiliation": "", "forename": "B", "identifier": "", "initials": "B", "lastname": "Albini" }, { "affiliation": "", "forename": "J J", "identifier": "", "initials": "JJ", "lastname": "Zambon" }, { "affiliation": "", "forename": "R J", "identifier": "", "initials": "RJ", "lastname": "Genco" } ]
1987-08
3305857
D000188:Actinobacillus / Q000276:immunology / Q000302:isolation & purification*; D000328:Adult; D010520:Aggressive Periodontitis / Q000382:microbiology*; D000942:Antigens, Bacterial / Q000032:analysis; D001431:Bacteriological Techniques; D005260:Female; D005455:Fluorescent Antibody Technique; D005881:Gingiva / Q000382:microbiology*; D006801:Humans; D008297:Male; D010510:Periodontal Diseases / Q000382:microbiology*
D003160:Comparative Study; D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S.
D000942:Antigens, Bacterial
10.1902/jop.1987.58.8.540
[]
false
eng
J Periodontol
8000345
0022-3492
United States
[ { "agency": "NIDCR NIH HHS", "country": "United States", "grant_acronym": "DE", "grant_id": "DE04898" } ]
"2024-08-13T08:46:10.109990Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Alteration in gastric mucosal acid protease activity induced by necrotizing agents and prevention by prostaglandin E2.
10(3)
128-34
Tissue levels of two gastric mucosal acid proteases, pepsinogen and cathepsin D-like acid proteinase, were determined in rat gastric mucosa damaged by various necrotizing agents and the protective effects of prostaglandins against these biological alterations were investigated. Gastric mucosal damage by each necrotizing agent used was associated with a marked decrease in tissue level of cathepsin D-like acid proteinase. Particularly, ethanol ingestion caused its significant reduction parallel to the production of gastric lesions in a time-dependent manner. On the other hand, mucosal pepsinogen level increased markedly only in ethanol-damaged gastric mucosa, indicating that this change was mediated by a different mechanism from that for cathepsin D-like enzyme. In rats pretreated with prostaglandin E2 and prostaglandin inducers before ethanol administration, these biological alterations of two enzymes were effectively prevented as were gastric lesions. However, ethanol ingestion caused these changes to occur to the same degree in both the necrotic and non-necrotic areas of glandular mucosa. It was considered that cathepsin D-like acid proteinase was released from damaged gastric mucosa through a direct action on cellular membrane different from vasoconstrictor and platelet aggregating actions mediated by arachidonic acid metabolites.
Journal of pharmacobio-dynamics
[ { "affiliation": "", "forename": "N", "identifier": "", "initials": "N", "lastname": "Muto" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Yamamoto" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Tani" } ]
1987-03
3305858
D000818:Animals; D016282:Aspartic Acid Endopeptidases; D002402:Cathepsin D / Q000032:analysis; D002852:Chromatography, Ion Exchange; D015232:Dinoprostone; D010450:Endopeptidases / Q000032:analysis*; D000431:Ethanol / Q000633:toxicity; D005753:Gastric Mucosa / Q000187:drug effects* / Q000201:enzymology / Q000473:pathology; D008297:Male; D009336:Necrosis; D010435:Pepsinogens / Q000032:analysis; D011458:Prostaglandins E / Q000494:pharmacology*; D051381:Rats; D011919:Rats, Inbred Strains
D016428:Journal Article
D010435:Pepsinogens; D011458:Prostaglandins E; D000431:Ethanol; D010450:Endopeptidases; D016282:Aspartic Acid Endopeptidases; D002402:Cathepsin D; D015232:Dinoprostone
10.1248/bpb1978.10.128
[]
false
eng
J Pharmacobiodyn
7901854
0386-846X
Japan
[]
"2024-08-13T08:46:10.111957Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Variances in pharmacokinetic parameters due to assay methods for beta-methyldigoxin.
10(5)
209-14
A digoxin radioimmunoassay (RIA) or fluorescence polarization immunoassay (FPIA) kit is frequently used in routine therapeutic drug monitoring (TDM) of beta-methyldigoxin (MD) by applying a calibration curve made using the corresponding digoxin calibrators. The variances in the plasma levels (61 samples) and pharmacokinetics (5 patients) due to these two different assay methods for MD were examined in our patients with congestive heart failure. Although the plasma levels of MD measured by these methods were well correlated (r = 0.956, p less than 0.001) to each other over a wide range, RIA showed significantly lower values (p less than 0.01) in the subtherapeutic range (less than 0.80 ng/ml), but significantly higher values (p less than 0.002) in the therapeutic and toxic ranges (0.80-2.00 and 2.00 less than ng/ml), respectively than FPIA. This trend occurred with increasing concentrations. When MD samples, spiked in normal human plasma, were analyzed by these methods, RIA showed almost true MD values and gave larger values than FPIA with a mean ratio of FPIA to RIA of 0.83. In contrast, normal plasma samples, each spiked with a MD metabolite such as digoxigenin-bisdigitoxide or digoxigenin-monodigitoxide, showed higher values by 10 to 22% in FPIA. These observations are in good agreement with the findings obtained in a pharmacokinetic study that RIA gave significantly higher levels than FPIA, only in the early stage after MD administration, resulting in a smaller total volume of distribution and a larger beta value in the elimination phase, as compared with FPIA.(ABSTRACT TRUNCATED AT 250 WORDS)
Journal of pharmacobio-dynamics
[ { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Goto" }, { "affiliation": "", "forename": "A", "identifier": "", "initials": "A", "lastname": "Suzuki" }, { "affiliation": "", "forename": "T", "identifier": "", "initials": "T", "lastname": "Terashima" }, { "affiliation": "", "forename": "I", "identifier": "", "initials": "I", "lastname": "Johno" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Kitazawa" } ]
1987-05
3305859
D000328:Adult; D000368:Aged; D000918:Antibody Specificity; D003429:Cross Reactions; D004077:Digoxin / Q000031:analogs & derivatives*; D005260:Female; D005454:Fluorescence Polarization; D005455:Fluorescent Antibody Technique; D006333:Heart Failure / Q000188:drug therapy / Q000378:metabolism; D006801:Humans; D007700:Kinetics; D008297:Male; D008520:Medigoxin / Q000032:analysis / Q000378:metabolism* / Q000627:therapeutic use; D008875:Middle Aged; D011863:Radioimmunoassay
D016428:Journal Article
D004077:Digoxin; D008520:Medigoxin
10.1248/bpb1978.10.209
[]
false
eng
J Pharmacobiodyn
7901854
0386-846X
Japan
[]
"2024-08-13T08:46:10.112913Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Regulation of L-carnitine metabolism in Escherichia coli.
27(3)
131-7
The metabolization of L-carnitine was studied using whole cells of Escherichia coli 044 K74. It showed features of an epigenetical control. L-carnitine and crotonobetaine were able to induce the carnitine-reducing system. Oxygen and nitrate as electron acceptors, gamma-butyrobetaine as final product of carnitine transformation in E. coli as well as glucose repress the carnitine metabolization. Other betaines and structurally related compounds did not show any effect neither as inductors nor as repressors.
Journal of basic microbiology
[ { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Jung" }, { "affiliation": "", "forename": "H", "identifier": "", "initials": "H", "lastname": "Jung" }, { "affiliation": "", "forename": "H P", "identifier": "", "initials": "HP", "lastname": "Kleber" } ]
1987
3305860
D000332:Aerobiosis; D000693:Anaerobiosis; D002331:Carnitine / Q000378:metabolism*; D003470:Culture Media; D004926:Escherichia coli / Q000378:metabolism*; D007700:Kinetics
D016428:Journal Article
D003470:Culture Media; D002331:Carnitine
10.1002/jobm.3620270303
[]
false
eng
J Basic Microbiol
8503885
0233-111X
Germany
[]
"2024-08-13T08:46:10.113856Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Celebrating 75 years of APMA 1912-1987.
77(8)
385-470
Journal of the American Podiatric Medical Association
[]
1987-08
3305863
D049673:History, 20th Century; D011032:Podiatry / Q000266:history*; D012955:Societies, Medical / Q000266:history*; D014481:United States
D016456:Historical Article; D016428:Journal Article
10.7547/87507315-77-8-385
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.114473Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Kinetics of hepatic transport of 4-methylumbelliferone in rats. Analysis by multiple indicator dilution method.
15(1)
25-38
Hepatic elimination of 4-methylumbelliferone (4-MU), which has been used as a model compound for conjugative metabolism, was studied by means of a multiple indicator dilution (MID) method in the isolated perfused rat liver. Using this method, three intrinsic hepatic clearances, CLint,inf, CLint,eff, and CLint,seq, which represent the influx, efflux, and sequestration processes, respectively, were obtained. When the dose was increased from a low dose (50 micrograms/rat liver) to a high dose (3000 micrograms/rat liver), the hepatic availability of 4-MU increased from 0.11 to 0.73. With increasing dose, the CLint,eff value increased approximately two times, while the CLint,seq value decreased to approximately one-third. The remarkable dose dependence of hepatic availability was due to nonlinearity in both CLint,eff and CLint,seq values. However, the CLint,inf value was almost independent of dose. The dose-dependent change in CLint,seq might be explained by the saturation of conjugative metabolism of 4-MU, while the increase in the CLint,eff value with increasing dose might be partly explained by the nonlinear tissue binding of 4-MU, since the tissue unbound fraction determined by an ultrafiltration method using liver homogenate increased approximately 1.5 times at higher concentration of 4-MU compared to that at lower concentrations. In addition, based on a comparison of the individual intrinsic clearances, i.e., CLint,inf, CLint,eff, and CLint,seq, the major determining process of the apparent hepatic intrinsic clearance of 4-MU is thought to be the sequestration process at the high dose. However, at the low dose, the membrane transport process (influx and efflux processes) as well as the sequestration process also determine the apparent hepatic intrinsic clearance.
Journal of pharmacokinetics and biopharmaceutics
[ { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Miyauchi" }, { "affiliation": "", "forename": "Y", "identifier": "", "initials": "Y", "lastname": "Sugiyama" }, { "affiliation": "", "forename": "Y", "identifier": "", "initials": "Y", "lastname": "Sawada" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Morita" }, { "affiliation": "", "forename": "T", "identifier": "", "initials": "T", "lastname": "Iga" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Hanano" } ]
1987-02
3305862
D000818:Animals; D001692:Biological Transport; D004912:Erythrocytes / Q000378:metabolism; D006923:Hymecromone / Q000097:blood / Q000378:metabolism*; D066298:In Vitro Techniques; D007457:Iodine Radioisotopes; D007700:Kinetics; D008099:Liver / Q000378:metabolism*; D008297:Male; D011485:Protein Binding; D011865:Radioisotope Dilution Technique; D051381:Rats; D011919:Rats, Inbred Strains; D012710:Serum Albumin, Bovine / Q000378:metabolism; D014468:Umbelliferones / Q000378:metabolism*
D016428:Journal Article
D007457:Iodine Radioisotopes; D014468:Umbelliferones; D012710:Serum Albumin, Bovine; D006923:Hymecromone
10.1007/BF01062937
[ { "citation": "J Pharmacokinet Biopharm. 1986 Feb;14(1):51-64", "pmid": "3746632" }, { "citation": "J Clin Invest. 1974 Feb;53(2):634-46", "pmid": "11344578" }, { "citation": "J Pharmacokinet Biopharm. 1984 Apr;12(2):129-47", "pmid": "6491897" }, { "citation": "Circ Res. 1970 Nov;27(5):739-64", "pmid": "4922275" }, { "citation": "J Pharmacobiodyn. 1986 Feb;9(2):117-24", "pmid": "3712212" }, { "citation": "Biochem Pharmacol. 1985 Apr 15;34(8):1325-9", "pmid": "3994749" }, { "citation": "Drug Metab Dispos. 1978 Nov-Dec;6(6):611-6", "pmid": "33021" }, { "citation": "Comput Methods Programs Biomed. 1985 May;20(1):51-61", "pmid": "3896632" }, { "citation": "Am J Physiol. 1964 Jul;207:13-26", "pmid": "14193577" }, { "citation": "J Pharmacokinet Biopharm. 1977 Dec;5(6):655-80", "pmid": "599412" }, { "citation": "J Clin Invest. 1973 May;52(5):991-1009", "pmid": "4573356" }, { "citation": "Am J Physiol. 1976 Sep;231(3):734-42", "pmid": "788526" }, { "citation": "Experientia. 1975 Mar 15;31(3):306-8", "pmid": "1090443" }, { "citation": "Am J Physiol. 1963 Apr;204:626-40", "pmid": "13949263" }, { "citation": "J Pharmacokinet Biopharm. 1977 Dec;5(6):625-53", "pmid": "599411" }, { "citation": "J Pharmacokinet Biopharm. 1973 Apr;1(2):123-36", "pmid": "4764426" }, { "citation": "Hepatology. 1981 Mar-Apr;1(2):99-106", "pmid": "7026402" }, { "citation": "Am J Physiol. 1979 Jun;236(6):E638-48", "pmid": "375751" }, { "citation": "Gastroenterology. 1982 Dec;83(6):1163-9", "pmid": "6751925" }, { "citation": "Am J Physiol. 1985 Jun;248(6 Pt 1):G702-8", "pmid": "2408485" }, { "citation": "Clin Pharmacol Ther. 1977 Nov;22(5 Pt 2):623-39", "pmid": "913029" } ]
false
eng
J Pharmacokinet Biopharm
0357115
0090-466X
United States
[]
"2024-08-13T08:46:10.116907Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Observations on clinical research in podiatric medicine.
77(8)
390-1
Journal of the American Podiatric Medical Association
[ { "affiliation": "", "forename": "R B", "identifier": "", "initials": "RB", "lastname": "Patterson" } ]
1987-08
3305864
D049672:History, 19th Century; D049673:History, 20th Century; D011032:Podiatry; D012106:Research / Q000266:history
D016456:Historical Article; D016428:Journal Article
10.7547/87507315-77-8-390
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.117715Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
History of podiatric medical education. An update.
77(8)
404-18
Journal of the American Podiatric Medical Association
[ { "affiliation": "", "forename": "C W", "identifier": "", "initials": "CW", "lastname": "Gibley" } ]
1987-08
3305865
D049673:History, 20th Century; D011032:Podiatry / Q000193:education* / Q000266:history / Q000639:trends; D012577:Schools, Medical / Q000266:history*; D014481:United States
D016456:Historical Article; D016428:Journal Article
10.7547/87507315-77-8-404
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.118159Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The evolution of a specialty. A study of podiatric surgery.
77(8)
419-27
Journal of the American Podiatric Medical Association
[ { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Levrio" } ]
1987-08
3305866
D002568:Certification; D005528:Foot / Q000601:surgery*; D049672:History, 19th Century; D049673:History, 20th Century; D006801:Humans; D011032:Podiatry / Q000193:education / Q000266:history*; D013038:Specialization / Q000266:history
D016456:Historical Article; D016428:Journal Article
10.7547/87507315-77-8-419
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.118664Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Surgical treatment of the bunion deformity. Yesterday, today, and tomorrow.
77(8)
428-30
Journal of the American Podiatric Medical Association
[ { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Gerbert" } ]
1987-08
3305867
D001174:Arthrodesis / Q000266:history; D006215:Hallux Valgus / Q000266:history / Q000601:surgery*; D049672:History, 19th Century; D049673:History, 20th Century; D006801:Humans; D008683:Metatarsophalangeal Joint / Q000601:surgery; D010027:Osteotomy / Q000266:history
D016456:Historical Article; D016428:Journal Article
10.7547/87507315-77-8-428
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.119312Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Deep space infections in the diabetic patient.
77(8)
431-43
Journal of the American Podiatric Medical Association
[ { "affiliation": "", "forename": "F D", "identifier": "", "initials": "FD", "lastname": "Goldman" } ]
1987-08
3305868
D001424:Bacterial Infections / Q000209:etiology / Q000601:surgery*; D048909:Diabetes Complications; D005534:Foot Diseases / Q000209:etiology / Q000601:surgery*; D006801:Humans
D016428:Journal Article; D016454:Review
10.7547/87507315-77-8-431
[]
false
eng
J Am Podiatr Med Assoc
8501423
1930-8264
United States
[]
"2024-08-13T08:46:10.119657Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Longitudinal study of postoperative astigmatism.
13(4)
381-8
A prospective longitudinal study of 503 eyes that had extracapsular cataract extraction with posterior chamber intraocular lens implantation was conducted. Each patient was followed for a minimum of one year. Data were collected, analyzed, and the following information ascertained: temporal behavior of induced keratometric and cylindrical changes, induced with-the-rule, against-the-rule, and oblique astigmatism, comparison of keratometric and refractive astigmatism, and the effect of cutting sutures upon induced astigmatism. Though a large amount of with-the-rule astigmatism was immediately induced after surgery, by the end of one year over 60% of patients shifted toward against-the-rule.
Journal of cataract and refractive surgery
[ { "affiliation": "", "forename": "J C", "identifier": "", "initials": "JC", "lastname": "Axt" } ]
1987-07
3305869
D001251:Astigmatism / Q000209:etiology* / Q000473:pathology / Q000503:physiopathology; D002387:Cataract Extraction / Q000009:adverse effects* / Q000379:methods; D003315:Cornea / Q000473:pathology; D006801:Humans; D007910:Lenses, Intraocular / Q000009:adverse effects; D008137:Longitudinal Studies; D011446:Prospective Studies; D013536:Suture Techniques
D016428:Journal Article
10.1016/s0886-3350(87)80036-6
[]
false
eng
J Cataract Refract Surg
8604171
0886-3350
United States
[]
"2024-08-13T08:46:10.120108Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Unwanted optical effects caused by intraocular lens positioning holes.
13(4)
421-3
The positioning holes in posterior chamber intraocular lenses (IOLs) are the source of many complaints from postoperative cataract patients with well-placed posterior chamber IOLs and otherwise excellent surgical results. Factors influencing which patients are most bothered are (1) size and reactivity of the pupil, (2) distance between the posterior surface of the iris and the anterior surface of the IOL, and (3) diameter of the IOL's clear optical zone. Eliminating the positioning holes is the best way to reduce or prevent the unwanted effects of these lenses.
Journal of cataract and refractive surgery
[ { "affiliation": "", "forename": "R A", "identifier": "", "initials": "RA", "lastname": "Landry" } ]
1987-07
3305871
D006801:Humans; D007910:Lenses, Intraocular / Q000009:adverse effects*; D008722:Methods; D011474:Prosthesis Design; D013536:Suture Techniques; D014786:Vision Disorders / Q000209:etiology*
D016428:Journal Article
10.1016/s0886-3350(87)80043-3
[]
false
eng
J Cataract Refract Surg
8604171
0886-3350
United States
[]
"2024-08-13T08:46:10.120573Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Gull-wing haptic design for posterior chamber intraocular lens.
13(4)
410-3
The current trend toward implantation of posterior chamber lenses within the capsular bag rather than the ciliary sulcus seems logical in light of the increasing evidence of uveal damage from sulcus fixated posterior chamber lenses. However, long-term, successful capsular bag fixation has not been demonstrated with current popular looped lenses of either flat or angulated styles. This report evaluated a new gull-wing loop design that seems to have advantages of both planar and angulated loop styles for support of posterior chamber lenses.
Journal of cataract and refractive surgery
[ { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Masket" } ]
1987-07
3305870
D006801:Humans; D007910:Lenses, Intraocular / Q000009:adverse effects; D008722:Methods; D011474:Prosthesis Design; D013536:Suture Techniques
D016428:Journal Article
10.1016/s0886-3350(87)80040-8
[]
false
eng
J Cataract Refract Surg
8604171
0886-3350
United States
[]
"2024-08-13T08:46:10.121930Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Drinking water microbiology. Committee on the Challenges of Modern Society (NATO/CCMS).
7(5-6)
1-365
Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer
[]
1987
3305861
D001419:Bacteria / Q000302:isolation & purification* / Q000472:pathogenicity; D006801:Humans; D014481:United States; D014871:Water Microbiology; D014881:Water Supply / Q000592:standards
D016428:Journal Article; D016454:Review
[]
false
eng
J Environ Pathol Toxicol Oncol
8501420
0731-8898
United States
[]
"2024-08-13T08:46:10.122412Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Le sens du futur or reading behind the writing on the wall.
13(4)
428-30
Journal of cataract and refractive surgery
[ { "affiliation": "", "forename": "D S", "identifier": "", "initials": "DS", "lastname": "Aron-Rosa" } ]
1987-07
3305872
D005602:France; D049673:History, 20th Century; D006801:Humans; D053685:Laser Therapy / Q000266:history*; D007834:Lasers / Q000266:history*; D013508:Ophthalmologic Surgical Procedures
D020493:Autobiography; D019215:Biography; D016456:Historical Article; D016428:Journal Article
10.1016/s0886-3350(87)80045-7
[]
false
eng
J Cataract Refract Surg
8604171
0886-3350
United States
[]
"2024-08-13T08:46:10.122894Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Visual aberrations caused by optic components of posterior chamber intraocular lenses.
13(4)
431-5
A 58-year-old airline pilot had cataract surgery with implantation of a posterior chamber intraocular lens with four positioning holes around the optic edge. During periods of maximum pupil dilation, such as at night, visual aberrations including glare, monocular diplopia, and haloes occurred and he was unable to work in his occupation. The symptoms were severe enough that lens exchange was required, and a posterior chamber lens with no positioning holes was successfully implanted. The symptoms immediately subsided postoperatively and his last known visual acuity was 20/15. This case, and the report of another patient with similar postoperative problems, illustrates that implantation of lens optics with a larger effective optical zone for posterior chamber lens implantation is desirable. This is particularly true now that younger, more active patients, many still engaged in occupations, are having lens implantations.
Journal of cataract and refractive surgery
[ { "affiliation": "", "forename": "D J", "identifier": "", "initials": "DJ", "lastname": "Apple" }, { "affiliation": "", "forename": "S B", "identifier": "", "initials": "SB", "lastname": "Lichtenstein" }, { "affiliation": "", "forename": "K", "identifier": "", "initials": "K", "lastname": "Heerlein" }, { "affiliation": "", "forename": "S L", "identifier": "", "initials": "SL", "lastname": "Letchinger" }, { "affiliation": "", "forename": "R B", "identifier": "", "initials": "RB", "lastname": "Park" }, { "affiliation": "", "forename": "R N", "identifier": "", "initials": "RN", "lastname": "Brems" }, { "affiliation": "", "forename": "K L", "identifier": "", "initials": "KL", "lastname": "Piest" } ]
1987-07
3305873
D002387:Cataract Extraction; D006801:Humans; D007910:Lenses, Intraocular / Q000009:adverse effects*; D008297:Male; D008722:Methods; D008875:Middle Aged; D011183:Postoperative Complications; D011474:Prosthesis Design; D012086:Reoperation; D013536:Suture Techniques / Q000295:instrumentation*; D014786:Vision Disorders / Q000209:etiology*; D014792:Visual Acuity
D002363:Case Reports; D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
10.1016/s0886-3350(87)80046-9
[]
false
eng
J Cataract Refract Surg
8604171
0886-3350
United States
[]
"2024-08-13T08:46:10.123531Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Synaptic inputs to immunohistochemically identified neurones in the submucous plexus of the guinea-pig small intestine.
381()
465-82
1. Electrophysiological recordings were made from neurones in the submucous plexus of the guinea-pig small intestine, and these neurones were classified according to their synaptic inputs. 2. The neurones from which recording were made were filled during the recording period with the fluorescent dye, Lucifer Yellow, so they could be re-identified after processing for immunohistochemical localization of vasoactive intestinal peptide (VIP). 3. The presence or absence of VIP-like immunoreactivity was determined for a total of 130 neurones whose synaptic inputs had been fully characterized and eighty-two were found to be VIP reactive. After the VIP reactivity had been assessed, the preparations were reprocessed to reveal immunoreactivity for neuropeptide Y (NPY) and a further twenty-three neurones (none of which were reactive for VIP) were found to be reactive for this peptide. Of the remaining twenty-five neurones, nineteen were not reactive for either VIP or NPY and six could not be re-identified after reprocessing. 4. Electrical stimulation of internodal strands evoked excitatory synaptic potentials lasting 20-30 ms (fast responses) in all but one of the 130 neurones studied. 5. Almost all the VIP-reactive neurones (seventy-eight of eighty-two cells) exhibited inhibitory synaptic potentials, ranging in amplitude from 2 to 30 mV and lasting 150-1500 ms, but few of the VIP-negative neurones had such responses (six of forty-eight cells). No inhibitory synaptic potentials could be evoked in any of the NPY-reactive neurones. 6. Most VIP-reactive neurones (sixty-nine) had a slow excitatory synaptic potential which could be evoked by a single stimulus, lasted 5-20 s and was associated with an increase in input resistance. Only one NPY-reactive neurone had a slow excitatory potential, but such potentials were seen in nine of the nineteen VIP-negative, NPY-negative neurones. 7. In nine of the twenty-three NPY-reactive neurones a single stimulus evoked an excitatory synaptic potential (intermediate excitatory synaptic potential) lasting 500-1500 ms and associated with a fall in the input resistance. None of the VIP-negative, NPY-negative neurones exhibited the intermediate excitatory potentials but it was not possible to determine whether such potentials could be evoked in VIP-reactive neurones because the inhibitory synaptic potentials would obscure such events. 8. It is concluded that neurochemically distinct populations of submucous neurones can be distinguished physiologically on the basis of the differing combinations of types of synaptic input they receive.
The Journal of physiology
[ { "affiliation": "", "forename": "J C", "identifier": "", "initials": "JC", "lastname": "Bornstein" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Costa" }, { "affiliation": "", "forename": "J B", "identifier": "", "initials": "JB", "lastname": "Furness" } ]
1986-12
3305874
D000200:Action Potentials; D000818:Animals; D005455:Fluorescent Antibody Technique; D006168:Guinea Pigs; D066298:In Vitro Techniques; D007546:Isoquinolines; D009433:Neural Inhibition; D009474:Neurons / Q000032:analysis / Q000502:physiology*; D009478:Neuropeptide Y / Q000032:analysis; D013368:Submucous Plexus / Q000166:cytology / Q000502:physiology*; D013569:Synapses / Q000502:physiology*; D013997:Time Factors; D014660:Vasoactive Intestinal Peptide / Q000032:analysis
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
D007546:Isoquinolines; D009478:Neuropeptide Y; D014660:Vasoactive Intestinal Peptide; C017475:lucifer yellow
10.1113/jphysiol.1986.sp016339
[ { "citation": "Neuroscience. 1979;4(2):305-10", "pmid": "34125" }, { "citation": "J Physiol. 1975 Oct;251(3):817-32", "pmid": "1185684" }, { "citation": "Histochemistry. 1980 Feb;65(2):157-65", "pmid": "6987197" }, { "citation": "Neuroscience. 1980;5(1):1-20", "pmid": "6154268" }, { "citation": "Clin Exp Pharmacol Physiol. 1981 Jul;8(4):327-33", "pmid": "7307351" }, { "citation": "Scand J Gastroenterol Suppl. 1982;71:169-70", "pmid": "6951279" }, { "citation": "Neuroscience. 1983 Apr;8(4):665-76", "pmid": "6306503" }, { "citation": "Cell Tissue Res. 1983;234(1):71-92", "pmid": "6416674" }, { "citation": "Gastroenterology. 1984 Apr;86(4):637-44", "pmid": "6199254" }, { "citation": "Am J Physiol. 1984 Mar;246(3 Pt 1):G263-7", "pmid": "6142654" }, { "citation": "J Physiol. 1984 Jun;351:313-25", "pmid": "6379150" }, { "citation": "J Physiol. 1984 Jun;351:343-61", "pmid": "6205143" }, { "citation": "J Physiol. 1984 Jun;351:363-78", "pmid": "6747869" }, { "citation": "Cell Tissue Res. 1984;237(2):329-36", "pmid": "6206951" }, { "citation": "J Neurosci. 1985 Mar;5(3):617-33", "pmid": "3973688" }, { "citation": "Neuroscience. 1984 Nov;13(3):911-9", "pmid": "6152033" }, { "citation": "J Physiol. 1985 Jan;358:17-33", "pmid": "2858586" }, { "citation": "Cell Tissue Res. 1985;241(1):155-63", "pmid": "3839715" }, { "citation": "Naunyn Schmiedebergs Arch Pharmacol. 1985 Nov;331(2-3):260-6", "pmid": "2418370" }, { "citation": "J Physiol. 1986 Jan;370:61-74", "pmid": "2870182" }, { "citation": "J Physiol. 1975 Jul;249(2):369-85", "pmid": "1177096" }, { "citation": "Proc Natl Acad Sci U S A. 1979 Nov;76(11):6009-11", "pmid": "42909" } ]
false
eng
J Physiol
0266262
0022-3751
England
[]
"2024-08-13T08:46:10.125003Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Static orthoses for the management of microstomia.
24(3)
35-42
Microstomia is a complication of facial burns, traumatic injuries, scleroderma, or surgical reconstructions involving the oral aperture. A variety of orthoses for the correction or prevention of microstomia are offered by dentists, occupational therapists, physical therapists, and other specialists. This paper provides an overview of the structural and clinical features of 12 common tissue-borne or tooth-borne microstomia appliances. The review is intended to facilitate the selection of suitable orthoses, and to indicate the need for interdisciplinary management of microstomia patients.
Journal of rehabilitation research and development
[ { "affiliation": "", "forename": "D L", "identifier": "", "initials": "DL", "lastname": "Carlow" }, { "affiliation": "", "forename": "T A", "identifier": "", "initials": "TA", "lastname": "Conine" }, { "affiliation": "", "forename": "P", "identifier": "", "initials": "P", "lastname": "Stevenson-Moore" } ]
1987
3305875
D006801:Humans; D008865:Microstomia / Q000534:rehabilitation*; D009059:Mouth Diseases / Q000534:rehabilitation*; D009989:Orthotic Devices
D016428:Journal Article; D016454:Review
10.1682/jrrd.1987.07.0035
[]
false
eng
J Rehabil Res Dev
8410047
0748-7711
United States
[]
"2024-08-13T08:46:10.127100Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Improved color matching of metal-ceramic restorations. Part I: A systematic method for shade determination.
58(2)
133-9
The inherent problems in present shade matching procedures and communication between dentist and ceramist have been discussed. These five areas of weakness include the observer, variable viewing conditions, commercially available shade guides, inadequate technology, and poor communication. A systematic procedure that breaks down shade selection to the elements of opaque, body, and incisal porcelain shades was presented. This method simplifies and adds clarity in the registration of shades, improving the communication chain between dentist and ceramist. The system is suggested as a means to overcome many of the inherent problems in shade selection and communication. This approach enhances the dentist-ceramist team's ability to esthetically match metal-ceramic restorations to the natural dentition. Future parts of this series will present procedures for improved communication and a system for porcelain application.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "J A", "identifier": "", "initials": "JA", "lastname": "Sorensen" }, { "affiliation": "", "forename": "T J", "identifier": "", "initials": "TJ", "lastname": "Torres" } ]
1987-08
3305877
D003116:Color; D003442:Crowns; D003776:Dental Porcelain; D003779:Denture Design / Q000295:instrumentation; D003829:Denture, Partial; D006801:Humans; D008027:Light; D014070:Tooth / Q000033:anatomy & histology
D016428:Journal Article
D003776:Dental Porcelain
10.1016/0022-3913(87)90163-6
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.127789Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Dynamic orthoses for the management of microstomia.
24(3)
43-8
Oral wounds and burns may result in microstomia with significant management problems. An important early management decision involves the selection of an appliance capable of applying forces that will halt and reverse the condition. A selection appropriate to the patient may be based on the need for teeth suitably placed to retain and position a particular device. Limited access to the patient's mouth because of recent trauma, surgery, wiring, inability to tolerate anesthetic, etc., may further restrict choices. Thus, the process of selection involves a weighing of the specific patient's condition and program of treatment against an understanding of the unique features, including complexity of fabrication and durability, of the range of prostheses available. This article provides an overview of the structural and clinical characteristics of seven dynamic intraoral and extraoral microstomia appliances. The need for interdisciplinary management of microstomia with appliances has been noted, and opportunities for research have been pointed out.
Journal of rehabilitation research and development
[ { "affiliation": "", "forename": "T A", "identifier": "", "initials": "TA", "lastname": "Conine" }, { "affiliation": "", "forename": "D L", "identifier": "", "initials": "DL", "lastname": "Carlow" }, { "affiliation": "", "forename": "P", "identifier": "", "initials": "P", "lastname": "Stevenson-Moore" } ]
1987
3305876
D006801:Humans; D008865:Microstomia / Q000534:rehabilitation*; D009059:Mouth Diseases / Q000534:rehabilitation*; D009989:Orthotic Devices
D016428:Journal Article; D016454:Review
10.1682/jrrd.1987.07.0043
[]
false
eng
J Rehabil Res Dev
8410047
0748-7711
United States
[]
"2024-08-13T08:46:10.128393Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The hemisected mandibular molar: a strategic abutment.
58(2)
140-5
The loss of a strategic distal abutment can result in the patient wearing a removable partial denture. The indications and techniques necessary to retain a hemisected mandibular molar as a fixed partial denture abutment are presented.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "S M", "identifier": "", "initials": "SM", "lastname": "Schmitt" }, { "affiliation": "", "forename": "F H", "identifier": "", "initials": "FH", "lastname": "Brown" } ]
1987-08
3305878
D003442:Crowns; D000044:Dental Abutments; D003766:Dental Occlusion; D003779:Denture Design; D003830:Denture, Partial, Fixed; D005881:Gingiva / Q000033:anatomy & histology; D006801:Humans; D008963:Molar / Q000601:surgery*; D012390:Root Canal Therapy; D014092:Tooth Root / Q000473:pathology / Q000601:surgery
D016428:Journal Article
10.1016/0022-3913(87)90164-8
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.129058Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Considerations for furcation treatment. Part III: Restorative therapy.
58(2)
145-7
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "R F", "identifier": "", "initials": "RF", "lastname": "Baima" } ]
1987-08
3305879
D003442:Crowns; D000044:Dental Abutments; D006801:Humans; D008963:Molar / Q000601:surgery*; D010510:Periodontal Diseases / Q000628:therapy; D011379:Prognosis; D014092:Tooth Root / Q000601:surgery*
D016428:Journal Article
10.1016/0022-3913(87)90165-x
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.129835Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A photoelastic study of stresses on porcelain laminate preparations.
58(2)
157-61
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Highton" }, { "affiliation": "", "forename": "A A", "identifier": "", "initials": "AA", "lastname": "Caputo" }, { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Mátyás" } ]
1987-08
3305880
D003776:Dental Porcelain; D003799:Dental Stress Analysis / Q000379:methods*; D003801:Dental Veneers; D003779:Denture Design; D006801:Humans; D007180:Incisor; D008954:Models, Biological; D013314:Stress, Mechanical
D016428:Journal Article
D003776:Dental Porcelain
10.1016/0022-3913(87)90168-5
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.130539Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The sealing capacity of intermediary base materials.
58(2)
166-70
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "H W", "identifier": "", "initials": "HW", "lastname": "Dippel" }, { "affiliation": "", "forename": "J M", "identifier": "", "initials": "JM", "lastname": "Borggreven" }, { "affiliation": "", "forename": "P M", "identifier": "", "initials": "PM", "lastname": "Hoppenbrouwers" } ]
1987-08
3305882
D002021:Buffers; D002710:Chlorhexidine / Q000494:pharmacology; D001840:Dental Bonding; D003736:Dental Cavity Lining; D003738:Dental Cements; D003804:Dentin / Q000502:physiology / Q000648:ultrastructure*; D003806:Dentin Permeability / Q000187:drug effects*; D006801:Humans; D013012:Sorbitol / Q000494:pharmacology; D014088:Tooth Permeability / Q000187:drug effects*
D016428:Journal Article
D002021:Buffers; D003738:Dental Cements; D013012:Sorbitol; D002710:Chlorhexidine
10.1016/0022-3913(87)90170-3
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.131055Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Comparing effects of tray treatment on the accuracy of dies.
58(2)
175-8
The effects of tray treatments on the accuracy of dies from addition silicone impressions were investigated. Tray treatments included custom acrylic resin tray with adhesive, perforated custom acrylic resin tray without adhesive, and perforated custom acrylic resin tray with adhesive. No appreciable differences were found in the complete crowns among the three tray treatments on the first pours. Significant statistical differences observed in the MOD and occlusal inlays were nonetheless of questionable clinical significance. Adhesives are advisable if the impressions are poured repeatedly, however, to minimize accidental separation of the impression from the tray. The second casts were less accurate with complete crowns and MOD inlays when perforated trays were used without adhesives.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "A H", "identifier": "", "initials": "AH", "lastname": "Tjan" }, { "affiliation": "", "forename": "S B", "identifier": "", "initials": "SB", "lastname": "Whang" } ]
1987-08
3305883
D000180:Acrylic Resins; D000269:Adhesives; D003442:Crowns; D003737:Dental Cavity Preparation; D003761:Dental Impression Technique / Q000295:instrumentation*; D004867:Equipment Design; D007284:Inlays; D003765:Models, Dental
D003160:Comparative Study; D016428:Journal Article
D000180:Acrylic Resins; D000269:Adhesives
10.1016/0022-3913(87)90172-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.132408Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A comparison of three restorative techniques for endodontically treated anterior teeth.
58(2)
161-5
An in vitro study of 45 teeth compared the failure loads of endodontically treated teeth restored with pin and amalgams, Para-Post dowel and composite, and glass ionomer/amalgam alloy coronal-radicular buildups. The following conclusions were made. The Para-Post and composite buildups exhibited the highest mean failure load, 35.3 kg. The mean failure load for pin and amalgam buildups was 27.9 kg. Glass ionomer/amalgam alloy coronal-radicular buildups exhibited the lowest mean failure load, 14.1 kg. Restoration of endodontically treated anterior teeth with glass ionomer/amalgam alloy coronal-radicular buildups is contraindicated.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "J L", "identifier": "", "initials": "JL", "lastname": "Brandal" }, { "affiliation": "", "forename": "J I", "identifier": "", "initials": "JI", "lastname": "Nicholls" }, { "affiliation": "", "forename": "G W", "identifier": "", "initials": "GW", "lastname": "Harrington" } ]
1987-08
3305881
D003442:Crowns; D003723:Dental Amalgam; D003772:Dental Pins; D003793:Dental Restoration, Permanent / Q000379:methods*; D005899:Glass Ionomer Cements; D006801:Humans; D007180:Incisor; D011176:Post and Core Technique; D012390:Root Canal Therapy; D013314:Stress, Mechanical
D003160:Comparative Study; D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
D005899:Glass Ionomer Cements; D003723:Dental Amalgam
10.1016/0022-3913(87)90169-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.132968Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Cast aluminum denture base.
58(2)
179-86
The laboratory procedures for a cast aluminum base denture have been presented. If an induction casting machine is not available, the "two-oven technique" works well, provided the casting arm is kept spinning manually for 4 minutes after casting. If laboratory procedures are executed precisely and with care, the aluminum base denture can be cast with good results.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "M T", "identifier": "", "initials": "MT", "lastname": "Barco" }, { "affiliation": "", "forename": "M L", "identifier": "", "initials": "ML", "lastname": "Dembert" } ]
1987-08
3305884
D000535:Aluminum; D003735:Dental Casting Technique; D003761:Dental Impression Technique; D003819:Denture Bases; D003779:Denture Design; D003824:Denture, Complete; D006801:Humans
D016428:Journal Article
D000535:Aluminum
10.1016/0022-3913(87)90173-9
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.133516Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
An investigation of shear bond strengths of various resin-bonded inner surface rest seat designs for removable partial dentures.
58(2)
186-94
Results and conclusions that can be drawn from this study are: All smooth, mesh, and seating preparation groups produced mean bond strengths significantly greater than that of the control group (p less than 0.01). The cast mesh rest seats exhibited significantly greater bond strengths at 24 hours (p = .0072). However, at 30 days, statistically significant differences between the three groups were not evident. Mean bond strengths for the electrolytically etched rest seat groups increased significantly at 30 days compared with the 24-hour means (p less than .05). These results suggest that an electrolytically etched resin-bonded rest seat can easily withstand the functional stresses exerted by a removable partial denture. The incorporation of seating preparation on an abutment tooth for an etched resin-bonded lingual rest seat seems to offer no advantage in terms of retentive strength.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "P W", "identifier": "", "initials": "PW", "lastname": "Seely" }, { "affiliation": "", "forename": "S E", "identifier": "", "initials": "SE", "lastname": "Windeler" }, { "affiliation": "", "forename": "B K", "identifier": "", "initials": "BK", "lastname": "Norling" } ]
1987-08
3305885
D000134:Acid Etching, Dental; D000818:Animals; D002417:Cattle; D000044:Dental Abutments; D001840:Dental Bonding; D003737:Dental Cavity Preparation; D003743:Dental Enamel; D003799:Dental Stress Analysis; D003832:Denture, Partial, Removable; D013314:Stress, Mechanical
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
10.1016/0022-3913(87)90174-0
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.134435Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A technique for the obturation of anterior maxillary defects with accompanying midfacial tissue loss.
58(2)
203-5
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "L", "identifier": "", "initials": "L", "lastname": "Fattore" }, { "affiliation": "", "forename": "D C", "identifier": "", "initials": "DC", "lastname": "Edmonds" } ]
1987-08
3305887
D003779:Denture Design; D003827:Denture, Complete, Upper; D005260:Female; D006801:Humans; D008447:Maxillofacial Prosthesis; D009666:Nose; D019736:Prostheses and Implants; D011474:Prosthesis Design
D016428:Journal Article
10.1016/0022-3913(87)90177-6
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.135010Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Significance of abutment tooth angle of gingival convergence on removable partial denture retention.
58(2)
194-6
The angle of gingival convergence is one of the many factors that influence the retention capability of removable partial denture clasps. A geometric evaluation of the retention properties of this angle has been presented.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "R L", "identifier": "", "initials": "RL", "lastname": "Schneider" } ]
1987-08
3305886
D000044:Dental Abutments; D003737:Dental Cavity Preparation; D003781:Denture Retention; D003832:Denture, Partial, Removable; D005881:Gingiva / Q000033:anatomy & histology*; D006801:Humans; D014070:Tooth / Q000033:anatomy & histology*
D016428:Journal Article
10.1016/0022-3913(87)90175-2
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.135721Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Limiting wax pattern distortion caused by setting expansion.
58(2)
229-34
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "D R", "identifier": "", "initials": "DR", "lastname": "Davis" } ]
1987-08
3305888
D002484:Cementation; D055598:Chemical Phenomena; D002627:Chemistry, Physical; D003442:Crowns; D003734:Dental Casting Investment; D003735:Dental Casting Technique; D007283:Inlay Casting Wax; D007284:Inlays; D003765:Models, Dental; D013499:Surface Properties; D014885:Waxes
D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S.
D003734:Dental Casting Investment; D014885:Waxes; D007283:Inlay Casting Wax
10.1016/0022-3913(87)90182-x
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[ { "agency": "NCRR NIH HHS", "country": "United States", "grant_acronym": "RR", "grant_id": "RR05305-23" } ]
"2024-08-13T08:46:10.136297Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Fabrication of a provisional complete denture.
58(2)
246-8
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "E M", "identifier": "", "initials": "EM", "lastname": "Langenwalter" }, { "affiliation": "", "forename": "R D", "identifier": "", "initials": "RD", "lastname": "Jordan" }, { "affiliation": "", "forename": "O", "identifier": "", "initials": "O", "lastname": "Espinoza" } ]
1987-08
3305889
D003779:Denture Design; D003827:Denture, Complete, Upper; D006801:Humans
D016428:Journal Article
10.1016/0022-3913(87)90185-5
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.137883Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Internal venting of castings to improve marginal seal and retention of castings.
58(3)
270-3
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "K J", "identifier": "", "initials": "KJ", "lastname": "Bruggers" }, { "affiliation": "", "forename": "H", "identifier": "", "initials": "H", "lastname": "Bruggers" } ]
1987-09
3305891
D002484:Cementation; D003442:Crowns; D003722:Dental Alloys; D003735:Dental Casting Technique; D003776:Dental Porcelain; D003779:Denture Design; D003781:Denture Retention; D006801:Humans; D013499:Surface Properties
D016428:Journal Article
D003722:Dental Alloys; D003776:Dental Porcelain
10.1016/0022-3913(87)90037-0
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.138528Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Effectiveness and durability of repaired acrylic resin joints.
58(2)
249-53
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "H D", "identifier": "", "initials": "HD", "lastname": "Stipho" }, { "affiliation": "", "forename": "A S", "identifier": "", "initials": "AS", "lastname": "Stipho" } ]
1987-08
3305890
D000180:Acrylic Resins; D055598:Chemical Phenomena; D002627:Chemistry, Physical; D003780:Denture Repair / Q000379:methods*; D003824:Denture, Complete; D013314:Stress, Mechanical
D016428:Journal Article
D000180:Acrylic Resins
10.1016/0022-3913(87)90186-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.139098Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Microleakage pattern of a resin-veneered glass-ionomer cavity liner.
58(3)
273-6
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "G A", "identifier": "", "initials": "GA", "lastname": "Crim" }, { "affiliation": "", "forename": "J S", "identifier": "", "initials": "JS", "lastname": "Shay" } ]
1987-09
3305892
D003188:Composite Resins; D001840:Dental Bonding; D003736:Dental Cavity Lining; D003738:Dental Cements; D003763:Dental Leakage / Q000175:diagnosis / Q000473:pathology / Q000517:prevention & control*; D003793:Dental Restoration, Permanent; D005899:Glass Ionomer Cements; D006801:Humans
D016428:Journal Article
D003188:Composite Resins; D003738:Dental Cements; D005899:Glass Ionomer Cements
10.1016/0022-3913(87)90038-2
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.139675Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Visual and instrumental discrimination steps between two adjacent porcelain shades.
58(3)
286-91
Two different porcelain systems were compared over the B1 to B2 shade ranges visually and spectrophotometrically. Six samples of each porcelain were made by blending weighed increments of opaque and body porcelain and firing the blended compositions onto Option metal disks according to manufacturer's instructions. Compositional blends varied incrementally by 20% in steps. Selective blending of porcelain shades was shown to have an effect in improving the range of choices within the shade guide system. The human eye was capable of detecting small-step changes between two steps of the Vita shade guide. Systematic color changes occurred with compositional changes between B1 and B2. It appears from the overall results observed that a desired blending of porcelains at smaller intervals than full shade guide steps could be done more easily with Jelenko than with Vita porcelain. The visual rankings agreed more closely with the manufacturer's expectations than did the instrumental measurements.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "G A", "identifier": "", "initials": "GA", "lastname": "Ecker" }, { "affiliation": "", "forename": "J B", "identifier": "", "initials": "JB", "lastname": "Moser" } ]
1987-09
3305893
D003116:Color; D003776:Dental Porcelain / Q000032:analysis; D003779:Denture Design / Q000295:instrumentation*; D008029:Lighting; D013053:Spectrophotometry; D013499:Surface Properties
D003160:Comparative Study; D016428:Journal Article
D003776:Dental Porcelain
10.1016/0022-3913(87)90042-4
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.140461Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Measuring the thickness of a paint-on die spacer.
58(3)
305-8
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "M R", "identifier": "", "initials": "MR", "lastname": "Rieger" }, { "affiliation": "", "forename": "R A", "identifier": "", "initials": "RA", "lastname": "Tanquist" }, { "affiliation": "", "forename": "M O", "identifier": "", "initials": "MO", "lastname": "Brose" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Ali" } ]
1987-09
3305895
D002133:Calcium Sulfate; D003442:Crowns; D003735:Dental Casting Technique / Q000295:instrumentation; D003779:Denture Design / Q000295:instrumentation*; D006047:Gold Alloys; D006801:Humans; D012834:Silver; D013499:Surface Properties
D016428:Journal Article
D006047:Gold Alloys; D012834:Silver; D002133:Calcium Sulfate
10.1016/0022-3913(87)90045-x
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.141295Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The effect of metal retentive designs on resin veneer retention.
58(3)
297-305
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "S L", "identifier": "", "initials": "SL", "lastname": "Shue" }, { "affiliation": "", "forename": "J I", "identifier": "", "initials": "JI", "lastname": "Nicholls" }, { "affiliation": "", "forename": "J D", "identifier": "", "initials": "JD", "lastname": "Townsend" } ]
1987-09
3305894
D000269:Adhesives; D003722:Dental Alloys; D001840:Dental Bonding / Q000379:methods; D003801:Dental Veneers; D003779:Denture Design; D003781:Denture Retention; D006801:Humans; D012117:Resins, Synthetic; D013718:Tensile Strength
D003160:Comparative Study; D016428:Journal Article
D000269:Adhesives; D003722:Dental Alloys; D012117:Resins, Synthetic
10.1016/0022-3913(87)90044-8
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.142035Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Using metal bases in making complete dentures.
58(3)
314-7
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "E J", "identifier": "", "initials": "EJ", "lastname": "Belfiglio" } ]
1987-09
3305897
D003722:Dental Alloys; D003819:Denture Bases; D003779:Denture Design; D003781:Denture Retention; D003824:Denture, Complete; D006801:Humans
D016428:Journal Article
D003722:Dental Alloys
10.1016/0022-3913(87)90047-3
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.143668Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Effects of various cementation methods on the retention of prefabricated posts.
58(3)
309-13
Para-Post dowels were cemented by using combinations of cement, cleansing agents, and dentinal treatments. The comparative retentive strengths were as follows: 1. Para-Post posts cemented with composite into mechanically corrugated post spaces recorded the greatest retention. 2. The retention of the posts cemented with composite into post spaces rinsed with 1 ml of 17% EDTA with a pH of 7.5 and followed immediately by 1 ml of 5.25% NaOCl was lowest. 3. The retention of the posts secured with zinc phosphate into mechanically corrugated post spaces was significantly higher than with untapped post spaces. 4. The retentive strength of the posts placed with glass-ionomer cement into post spaces, irrigated with 1 ml of 40% polyacrylic acid solution, and rinsed with distilled water was comparable to that of posts secured with zinc phosphate cement without roughened post spaces.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "A H", "identifier": "", "initials": "AH", "lastname": "Tjan" }, { "affiliation": "", "forename": "A H", "identifier": "", "initials": "AH", "lastname": "Tjan" }, { "affiliation": "", "forename": "J H", "identifier": "", "initials": "JH", "lastname": "Greive" } ]
1987-09
3305896
D002484:Cementation / Q000379:methods*; D003188:Composite Resins; D003442:Crowns; D003738:Dental Cements; D003779:Denture Design; D003781:Denture Retention; D005899:Glass Ionomer Cements; D006801:Humans; D011176:Post and Core Technique; D011897:Random Allocation; D013499:Surface Properties; D015036:Zinc Phosphate Cement
D016430:Clinical Trial; D003160:Comparative Study; D018848:Controlled Clinical Trial; D016428:Journal Article
D003188:Composite Resins; D003738:Dental Cements; D005899:Glass Ionomer Cements; D015036:Zinc Phosphate Cement
10.1016/0022-3913(87)90046-1
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.144508Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A classification of precision attachments.
58(3)
322-7
This overview of attachments is intended to provide an explanation of the design characteristics of 13 different groups. The clinical situation for which an attachment is intended will place specific demands that can be met more closely if the forces acting on the prosthesis are considered. No universal or ideal design is available, so if attachments are used, they should be selected from the group with the most suitable characteristics for the task required. The stress-breaking effect of attachments is vague. They offer a potential for rotational and resilient movement between the prosthesis and the abutment teeth, but the amount of stress that must be broken to protect the periodontium of the teeth may exceed the capabilities of any particular attachment used. Nevertheless, attachments can provide an effective answer to prosthesis stability and retention in a way that is cosmetically pleasing.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Becerra" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "MacEntee" } ]
1987-09
3305898
D003779:Denture Design; D003834:Denture Precision Attachment / Q000145:classification; D006801:Humans; D008280:Magnetics
D016428:Journal Article
10.1016/0022-3913(87)90049-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.145124Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Effect on the fit of removable partial denture frameworks when master casts are treated with cyanoacrylate resin.
58(3)
327-9
Master casts of improved dental stone were made from irreversible hydrocolloid impressions of a metal model. Half of the master casts were treated with cyanoacrylate resin and half were untreated controls. They were sent to a dental laboratory for framework fabrication. The returned frameworks were examined for acceptability and their completeness of seating was determined. The frameworks fabricated on the treated master casts fit significantly better than the controls. The improved seating may be attributed to an increased surface hardness, increased abrasion resistance, and improved surface morphology, but further study is necessary.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "M J", "identifier": "", "initials": "MJ", "lastname": "Calverley" }, { "affiliation": "", "forename": "J R", "identifier": "", "initials": "JR", "lastname": "Moergeli" } ]
1987-09
3305899
D003487:Cyanoacrylates; D003735:Dental Casting Technique; D003779:Denture Design; D003781:Denture Retention; D003832:Denture, Partial, Removable; D003765:Models, Dental; D013499:Surface Properties
D016428:Journal Article
D003487:Cyanoacrylates
10.1016/0022-3913(87)90050-3
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.145986Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Fatigue failure in acrylic resin retaining minor connectors.
58(3)
329-35
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "D T", "identifier": "", "initials": "DT", "lastname": "Brown" }, { "affiliation": "", "forename": "R P", "identifier": "", "initials": "RP", "lastname": "Desjardins" }, { "affiliation": "", "forename": "E Y", "identifier": "", "initials": "EY", "lastname": "Chao" } ]
1987-09
3305900
D000180:Acrylic Resins; D003779:Denture Design; D003832:Denture, Partial, Removable; D006801:Humans; D008422:Materials Testing; D013314:Stress, Mechanical; D013499:Surface Properties
D003160:Comparative Study; D016428:Journal Article
D000180:Acrylic Resins
10.1016/0022-3913(87)90051-5
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.146698Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Design variations of the rotational path removable partial denture.
58(3)
336-8
The rotational path removable partial denture is a convenient design to use when restoring anterior edentulous spaces and can produce excellent esthetic results. In situations that are not ideal for the conventional rotational path, design alterations can be made that will allow the same excellent results to be achieved.
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "R S", "identifier": "", "initials": "RS", "lastname": "Schwartz" }, { "affiliation": "", "forename": "D G", "identifier": "", "initials": "DG", "lastname": "Murchison" } ]
1987-09
3305901
D003779:Denture Design; D003781:Denture Retention; D003832:Denture, Partial, Removable; D006801:Humans; D012399:Rotation
D016428:Journal Article
10.1016/0022-3913(87)90052-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.147403Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
A radiographic analysis of a mandibular anterior vestibuloplasty with free skin graft.
58(3)
374-9
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "C J", "identifier": "", "initials": "CJ", "lastname": "Watson" } ]
1987-09
3305903
D000328:Adult; D000539:Alveolar Process / Q000000981:diagnostic imaging* / Q000473:pathology; D001862:Bone Resorption / Q000000981:diagnostic imaging* / Q000473:pathology; D002508:Cephalometry; D003287:Contrast Media; D006801:Humans; D008046:Lip / Q000033:anatomy & histology; D008336:Mandibular Diseases / Q000000981:diagnostic imaging* / Q000473:pathology; D008875:Middle Aged; D011862:Radiography, Panoramic; D016038:Skin Transplantation; D014727:Vestibuloplasty / Q000379:methods
D016428:Journal Article
D003287:Contrast Media
10.1016/0022-3913(87)90061-8
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.148157Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Coordinated intraoral and extraoral prostheses in the rehabilitation of the orofacial cancer patient.
58(3)
343-8
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Birnbach" }, { "affiliation": "", "forename": "G L", "identifier": "", "initials": "GL", "lastname": "Herman" } ]
1987-09
3305902
D003779:Denture Design; D003829:Denture, Partial; D005153:Facial Neoplasms / Q000534:rehabilitation*; D006801:Humans; D008297:Male; D008447:Maxillofacial Prosthesis; D009666:Nose; D010158:Palatal Obturators; D010347:Patient Care Planning; D019736:Prostheses and Implants; D011474:Prosthesis Design
D016428:Journal Article
10.1016/0022-3913(87)90054-0
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.150036Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Transcutaneous electrical nerve stimulation in dentistry: a report of a double-blind study.
58(3)
379-83
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "F B", "identifier": "", "initials": "FB", "lastname": "Curcio" }, { "affiliation": "", "forename": "V M", "identifier": "", "initials": "VM", "lastname": "Tackney" }, { "affiliation": "", "forename": "R", "identifier": "", "initials": "R", "lastname": "Berweger" } ]
1987-09
3305904
D000766:Anesthesia, Dental / Q000295:instrumentation; D000772:Anesthesia, Local; D002986:Clinical Trials as Topic; D004311:Double-Blind Method; D004599:Electric Stimulation Therapy / Q000295:instrumentation; D004867:Equipment Design; D005260:Female; D006801:Humans; D008297:Male; D010146:Pain / Q000517:prevention & control*; D010919:Placebos; D004561:Transcutaneous Electric Nerve Stimulation / Q000295:instrumentation
D016430:Clinical Trial; D018848:Controlled Clinical Trial; D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't
D010919:Placebos
10.1016/0022-3913(87)90062-x
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.150826Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The effect of an air polishing device on sealant bond strength.
58(3)
384-7
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "L", "identifier": "", "initials": "L", "lastname": "Scott" }, { "affiliation": "", "forename": "D", "identifier": "", "initials": "D", "lastname": "Greer" } ]
1987-09
3305905
D001840:Dental Bonding; D003743:Dental Enamel / Q000033:anatomy & histology; D003777:Dental Prophylaxis / Q000295:instrumentation*; D006801:Humans; D007101:Immersion; D008422:Materials Testing / Q000379:methods; D010895:Pit and Fissure Sealants; D011897:Random Allocation; D013718:Tensile Strength; D014867:Water
D016428:Journal Article
D010895:Pit and Fissure Sealants; D014867:Water
10.1016/0022-3913(87)90063-1
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.151544Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
An investigation of the adhesion of acrylic resin teeth to dentures.
58(3)
389-92
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "M H", "identifier": "", "initials": "MH", "lastname": "Spratley" } ]
1987-09
3305906
D000268:Adhesiveness; D001840:Dental Bonding; D003776:Dental Porcelain; D003779:Denture Design; D003778:Dentures; D006801:Humans; D013314:Stress, Mechanical; D014093:Tooth, Artificial
D016428:Journal Article
D003776:Dental Porcelain
10.1016/0022-3913(87)90065-5
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.152332Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
An aid for swing-lock partial denture removal.
58(3)
393
The Journal of prosthetic dentistry
[ { "affiliation": "", "forename": "T L", "identifier": "", "initials": "TL", "lastname": "LaBell" }, { "affiliation": "", "forename": "A H", "identifier": "", "initials": "AH", "lastname": "Glassman" } ]
1987-09
3305907
D003779:Denture Design; D003832:Denture, Partial, Removable; D004867:Equipment Design; D006801:Humans; D012656:Self-Help Devices
D016428:Journal Article
10.1016/0022-3913(87)90066-7
[]
false
eng
J Prosthet Dent
0376364
0022-3913
United States
[]
"2024-08-13T08:46:10.152886Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The influence of psychiatric, psychological and social factors on the control of insulin-dependent diabetes mellitus.
31(3)
277-86
Journal of psychosomatic research
[ { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Wilkinson" } ]
1987
3305908
D003072:Cognition Disorders / Q000523:psychology; D003376:Counseling; D003922:Diabetes Mellitus, Type 1 / Q000523:psychology*; D006801:Humans; D008016:Life Change Events; D010551:Personality; D011613:Psychotherapy; D012940:Social Problems
D016428:Journal Article; D016454:Review
10.1016/0022-3999(87)90047-x
[]
false
eng
J Psychosom Res
0376333
0022-3999
England
[]
"2024-08-13T08:46:10.153483Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Post-translational acquisition of ligand binding- and tyrosine kinase-domain function by the epidermal growth factor and insulin receptors.
7(1-4)
321-54
The epidermal growth factor receptor (EGFR) and insulin receptor undergo slow post-translational modification by which they acquire hormone binding and tyrosine kinase (EGFR) function. The half-time for acquisition of EGF or insulin binding activity is 30-40 min and of tyrosine kinase activity (EGFR), is 10-15 min. Tunicamycin, an inhibitor of N-linked oligosaccharide addition, blocks acquisition of both EGF and insulin binding activity. With EGFR, activation precedes acquisition of resistance to endoglucosaminidase H (t1/2 approximately equal to 75 min), a medial Golgi event. Treatment of active high mannose receptor with endo H generates fully active aglyco-receptor; thus, core oligosaccharide addition is a prerequisite for activation, but not for EGF binding per se. EGFR is activated in and translocated from the endoplasmic reticulum (ER) slowly (t1/2 approximately equal to 75 min). Since translocation rate equals the rate for acquisition of endo H resistance, transit from the ER is rate limiting for EGFR maturation. Tunicamycin inhibits exit from the ER parallel to its effect on acquisition of binding activity. Insulin proreceptor, a 210 kDa high-mannose glycopolypeptide, acquires insulin binding function (t1/2 approximately equal to 45 min) then is proteolytically cleaved (t1/2 approximately equal to 3 hr) into subunits of the mature alpha 2 beta 2 receptor. Modification giving rise to insulin binding activity is due to a conformational change in the binding domain, since human autoimmune antibody recognizes only the active species, while rabbit polyclonal antibody recognizes all forms. Newly-translated EGF proreceptor lacks a functional tyrosine domain capable of autophosphorylation; 30-40 min after translation, while still in the ER, tyrosine kinase activity is acquired. Since the kinase domain is cytoplasmic, the receptor may become phosphorylated on tyrosine before reaching the plasma membrane.
Journal of receptor research
[ { "affiliation": "", "forename": "M D", "identifier": "", "initials": "MD", "lastname": "Lane" }, { "affiliation": "", "forename": "L J", "identifier": "", "initials": "LJ", "lastname": "Slieker" }, { "affiliation": "", "forename": "T S", "identifier": "", "initials": "TS", "lastname": "Olson" }, { "affiliation": "", "forename": "T M", "identifier": "", "initials": "TM", "lastname": "Martensen" } ]
1987
3305909
D000273:Adipose Tissue / Q000166:cytology; D001665:Binding Sites; D002294:Carcinoma, Squamous Cell; D002460:Cell Line; D004721:Endoplasmic Reticulum / Q000378:metabolism; D004815:Epidermal Growth Factor / Q000378:metabolism*; D066246:ErbB Receptors / Q000378:metabolism*; D006023:Glycoproteins / Q000378:metabolism; D006801:Humans; D007328:Insulin / Q000378:metabolism*; D007700:Kinetics; D008954:Models, Biological; D010766:Phosphorylation; D011485:Protein Binding; D011487:Protein Conformation; D011499:Protein Processing, Post-Translational / Q000187:drug effects; D011505:Protein-Tyrosine Kinases / Q000378:metabolism*; D011972:Receptor, Insulin / Q000378:metabolism*; D014415:Tunicamycin / Q000494:pharmacology
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D013487:Research Support, U.S. Gov't, P.H.S.
D006023:Glycoproteins; D007328:Insulin; D014415:Tunicamycin; D004815:Epidermal Growth Factor; D066246:ErbB Receptors; D011505:Protein-Tyrosine Kinases; D011972:Receptor, Insulin
10.3109/10799898709054992
[]
false
eng
J Recept Res
8008358
0197-5110
United States
[ { "agency": "NIADDK NIH HHS", "country": "United States", "grant_acronym": "AM", "grant_id": "AM-07319" }, { "agency": "NIADDK NIH HHS", "country": "United States", "grant_acronym": "AM", "grant_id": "AM-14574" }, { "agency": "NIGMS NIH HHS", "country": "United States", "grant_acronym": "GM", "grant_id": "GM-00184" } ]
"2024-08-13T08:46:10.155610Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
The human insulin receptor cDNA: a new tool to study the function of this receptor.
7(1-4)
377-404
The human insulin receptor (hIR) is an integral transmembrane glycoprotein comprised of two alpha and two beta subunits. An immediate consequence of insulin binding to the extracellular alpha subunit is the autophosphorylation of tyrosine residues on the intracellular domain of the beta subunit. The placental hIR cDNA has been cloned and sequenced, providing the primary structural features of the protein. In order to investigate the functions of the beta subunit and particularly the role of autophosphorylation and tyrosine phosphokinase (TPK) activity (a feature shared by other receptors and oncogene proteins) in transmembrane signalling, we designed an expression system of the hIR cDNA in eucaryotic cells. Superexpressing CHO cell lines that contain about 10(6) functional hIR/cell have been developed. In these cells half maximum stimulation of glucose uptake occurs at 5 X 10(-10)M insulin, whereas normal CHO cells require 5 X 10(-12)M insulin. In this expression system we have carried out site-directed mutagenesis experiments in which domains of the molecule have been deleted or particular amino acids have been replaced by others. The replacement of either or both the tyrosine residues 1162 and 1163 compromise an autophosphorylated site that is important for kinase function and the insulin response. Expression of an isolated membrane-bound form of the beta-subunit produces a 6 fold increase in glucose uptake. This insulin-independent effect disappears if the twin tyrosines are mutated or if the beta subunit is expressed in the cytoplasm. These studies also show that the C terminal 112 amino acid portion of the beta subunit is important for the stability of this protein.
Journal of receptor research
[ { "affiliation": "", "forename": "E", "identifier": "", "initials": "E", "lastname": "Clauser" }, { "affiliation": "", "forename": "L", "identifier": "", "initials": "L", "lastname": "Ellis" }, { "affiliation": "", "forename": "D", "identifier": "", "initials": "D", "lastname": "Morgan" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Edery" }, { "affiliation": "", "forename": "R A", "identifier": "", "initials": "RA", "lastname": "Roth" }, { "affiliation": "", "forename": "W J", "identifier": "", "initials": "WJ", "lastname": "Rutter" } ]
1987
3305910
D000595:Amino Acid Sequence; D000818:Animals; D002460:Cell Line; D006224:Cricetinae; D003412:Cricetulus; D004247:DNA / Q000235:genetics; D005260:Female; D005347:Fibroblasts / Q000378:metabolism; D006801:Humans; D007328:Insulin / Q000378:metabolism; D010053:Ovary; D010766:Phosphorylation; D011505:Protein-Tyrosine Kinases / Q000235:genetics / Q000378:metabolism; D011972:Receptor, Insulin / Q000235:genetics* / Q000378:metabolism; D011994:Recombinant Proteins / Q000235:genetics / Q000378:metabolism
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D013487:Research Support, U.S. Gov't, P.H.S.
D007328:Insulin; D011994:Recombinant Proteins; D004247:DNA; D011505:Protein-Tyrosine Kinases; D011972:Receptor, Insulin
10.3109/10799898709054994
[]
false
eng
J Recept Res
8008358
0197-5110
United States
[ { "agency": "NIADDK NIH HHS", "country": "United States", "grant_acronym": "AM", "grant_id": "AM21344" }, { "agency": "NIADDK NIH HHS", "country": "United States", "grant_acronym": "AM", "grant_id": "AM34926" }, { "agency": "NIGMS NIH HHS", "country": "United States", "grant_acronym": "GM", "grant_id": "GM28520" } ]
"2024-08-13T08:46:10.156685Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Control of GnRH secretion.
34()
1-8
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "I J", "identifier": "", "initials": "IJ", "lastname": "Clarke" } ]
1987
3305911
D000818:Animals; D005246:Feedback; D005260:Female; D006728:Hormones / Q000502:physiology; D008722:Methods; D010053:Ovary / Q000502:physiology; D010906:Pituitary Hormone-Releasing Hormones / Q000378:metabolism*; D012756:Sheep / Q000378:metabolism*
D016428:Journal Article; D016454:Review
D006728:Hormones; D010906:Pituitary Hormone-Releasing Hormones
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.157338Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Spermatogenesis and Sertoli cell numbers and function in rams and bulls.
34()
101-14
The two main types of cellular associations (type I, 2 generations of spermatocytes + 1 of spermatids; type II, 1 of spermatocytes and 2 of spermatids) occupy, respectively, more than half and about a third of the seminiferous epithelium cycle in rams and bulls. However, the duration of the cycle of the seminiferous epithelium and that of spermatogenesis differ between the species. A1 spermatogonia and Sertoli cell total numbers are highly correlated in adult rams and bulls. Mitosis in Sertoli cells occurs mostly in utero but may still occur for a short period after birth. Between birth and puberty there is about a 5-fold increase in the number of Sertoli cells. After that there are no seasonal- or age-related increases in the number of adult Sertoli cells. Some factors (season of birth; nutrition; genetics; hormones) affect mitosis of Sertoli cells in prepubertal animals. Sertoli cells differentiate after cessation of mitosis. Their differentiation is affected by cryptorchidism, nutrition, genetics and hormones. Their adult function is only poorly known. ABP and rete testis fluid secretions and nuclear Sertoli volume fluctuate under the influence of the same factors, but they are not always linked together. This reinforces the need for more knowledge of Sertoli cell secretions and function.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "M T", "identifier": "", "initials": "MT", "lastname": "Hochereau-de Reviers" }, { "affiliation": "", "forename": "C", "identifier": "", "initials": "C", "lastname": "Monet-Kuntz" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Courot" } ]
1987
3305912
D000818:Animals; D002417:Cattle / Q000502:physiology*; D002452:Cell Count; D002454:Cell Differentiation; D008297:Male; D012708:Sertoli Cells / Q000166:cytology* / Q000502:physiology; D012756:Sheep / Q000502:physiology*; D013091:Spermatogenesis
D016428:Journal Article; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.158236Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Function of the epididymis in bulls and rams.
34()
115-31
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "R P", "identifier": "", "initials": "RP", "lastname": "Amann" } ]
1987
3305913
D000818:Animals; D002417:Cattle / Q000502:physiology*; D004822:Epididymis / Q000033:anatomy & histology / Q000378:metabolism / Q000502:physiology*; D004848:Epithelium / Q000033:anatomy & histology / Q000378:metabolism; D008297:Male; D012756:Sheep / Q000502:physiology*
D016428:Journal Article; D013486:Research Support, U.S. Gov't, Non-P.H.S.; D013487:Research Support, U.S. Gov't, P.H.S.; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[ { "agency": "NICHD NIH HHS", "country": "United States", "grant_acronym": "HD", "grant_id": "HD-14,501" } ]
"2024-08-13T08:46:10.159014Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Changes in sperm surfaces associated with epididymal transit.
34()
133-49
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "R H", "identifier": "", "initials": "RH", "lastname": "Hammerstedt" }, { "affiliation": "", "forename": "J E", "identifier": "", "initials": "JE", "lastname": "Parks" } ]
1987
3305914
D000818:Animals; D002417:Cattle / Q000033:anatomy & histology* / Q000502:physiology; D002462:Cell Membrane / Q000502:physiology; D004822:Epididymis / Q000166:cytology*; D008297:Male; D008560:Membrane Fluidity; D012756:Sheep / Q000033:anatomy & histology* / Q000502:physiology; D013094:Spermatozoa / Q000648:ultrastructure*; D013552:Swine / Q000033:anatomy & histology
D016428:Journal Article; D013487:Research Support, U.S. Gov't, P.H.S.; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[ { "agency": "NICHD NIH HHS", "country": "United States", "grant_acronym": "HD", "grant_id": "NICHD-13099" }, { "agency": "NICHD NIH HHS", "country": "United States", "grant_acronym": "HD", "grant_id": "NICHD-18628" } ]
"2024-08-13T08:46:10.159641Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
In-vitro fertilization of ruminants.
34()
151-65
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "N L", "identifier": "", "initials": "NL", "lastname": "First" }, { "affiliation": "", "forename": "J J", "identifier": "", "initials": "JJ", "lastname": "Parrish" } ]
1987
3305915
D000818:Animals; D002417:Cattle / Q000502:physiology; D004622:Embryo, Mammalian / Q000502:physiology; D005314:Embryonic and Fetal Development; D005260:Female; D005307:Fertilization in Vitro; D008297:Male; D009865:Oocytes / Q000166:cytology; D012418:Ruminants / Q000502:physiology*; D013094:Spermatozoa / Q000502:physiology
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D013487:Research Support, U.S. Gov't, P.H.S.; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[ { "agency": "NICHD NIH HHS", "country": "United States", "grant_acronym": "HD", "grant_id": "HD-18345-02" } ]
"2024-08-13T08:46:10.161318Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Neurotransmitter regulation of luteinizing hormone and prolactin secretion.
34()
17-26
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "R A", "identifier": "", "initials": "RA", "lastname": "Dailey" }, { "affiliation": "", "forename": "D R", "identifier": "", "initials": "DR", "lastname": "Deaver" }, { "affiliation": "", "forename": "R L", "identifier": "", "initials": "RL", "lastname": "Goodman" } ]
1987
3305917
D000818:Animals; D001679:Biogenic Amines / Q000494:pharmacology*; D002395:Catecholamines / Q000037:antagonists & inhibitors; D002417:Cattle / Q000378:metabolism; D005260:Female; D007986:Luteinizing Hormone / Q000378:metabolism*; D008297:Male; D011388:Prolactin / Q000378:metabolism*; D012756:Sheep / Q000378:metabolism*
D016428:Journal Article; D016454:Review
D001679:Biogenic Amines; D002395:Catecholamines; D011388:Prolactin; D007986:Luteinizing Hormone
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.161975Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Endocrine regulation of puberty in cows and ewes.
34()
167-86
Sexual maturation in cows and ewes is modulated through changes in hypothalamic inhibition. This inhibition results in little or no stimulation of the release of gonadotrophins from the anterior pituitary. The ovary has a primary role in inhibiting gonadotrophin secretion during the prepubertal period and the responsiveness to the negative feedback effects of oestrogen decreases during the peripubertal period. There is also an increased secretion of ovarian progesterone during the peripubertal period but its role in the process of sexual maturation is not clear. Photoperiodic cues and dietary intake act upon the hypothalamus to modulate gonadotrophin secretion during sexual maturation and, in turn, influence the time when puberty occurs.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "J E", "identifier": "", "initials": "JE", "lastname": "Kinder" }, { "affiliation": "", "forename": "M L", "identifier": "", "initials": "ML", "lastname": "Day" }, { "affiliation": "", "forename": "R J", "identifier": "", "initials": "RJ", "lastname": "Kittok" } ]
1987
3305916
D000818:Animals; D002417:Cattle / Q000502:physiology*; D005260:Female; D006062:Gonadotropins / Q000378:metabolism; D006728:Hormones / Q000502:physiology*; D008027:Light; D010053:Ovary / Q000502:physiology; D010902:Pituitary Gland / Q000502:physiology; D012741:Sexual Maturation; D012756:Sheep / Q000502:physiology*
D016428:Journal Article; D016454:Review
D006062:Gonadotropins; D006728:Hormones
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.162674Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Photoperiodic control of the onset of breeding activity and fecundity in ewes.
34()
187-99
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "D J", "identifier": "", "initials": "DJ", "lastname": "Kennaway" }, { "affiliation": "", "forename": "E A", "identifier": "", "initials": "EA", "lastname": "Dunstan" }, { "affiliation": "", "forename": "L D", "identifier": "", "initials": "LD", "lastname": "Staples" } ]
1987
3305918
D000818:Animals; D001947:Breeding; D005260:Female; D005298:Fertility / Q000187:drug effects; D008027:Light; D008550:Melatonin / Q000494:pharmacology; D012621:Seasons; D012756:Sheep / Q000502:physiology*
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D016454:Review
D008550:Melatonin
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.163495Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Function of the hypothalamic-hypophysial axis during the post-partum period in ewes and cows.
34()
201-13
During pregnancy the hypothalamic-hypophysial axis is suppressed by the high concentrations of progesterone and oestradiol in the circulation. The high concentrations of these steroids appear to inhibit secretion of GnRH from the hypothalamus, resulting in inadequate stimulation of pituitary gonadotrophs to maintain synthesis of LH. This produces a depletion of LH in the anterior pituitary gland that must be restored after parturition before normal oestrous cycles can begin.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "T M", "identifier": "", "initials": "TM", "lastname": "Nett" } ]
1987
3305919
D000780:Anestrus / Q000378:metabolism*; D000818:Animals; D002417:Cattle / Q000378:metabolism*; D004971:Estrus / Q000378:metabolism*; D005260:Female; D007030:Hypothalamo-Hypophyseal System / Q000378:metabolism*; D007774:Lactation / Q000378:metabolism; D007986:Luteinizing Hormone / Q000378:metabolism*; D010903:Pituitary Gland, Anterior / Q000378:metabolism; D049590:Postpartum Period / Q000378:metabolism*; D011247:Pregnancy; D012756:Sheep / Q000378:metabolism*
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D013486:Research Support, U.S. Gov't, Non-P.H.S.; D013487:Research Support, U.S. Gov't, P.H.S.; D016454:Review
D007986:Luteinizing Hormone
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[ { "agency": "NICHD NIH HHS", "country": "United States", "grant_acronym": "HD", "grant_id": "HD-07841" } ]
"2024-08-13T08:46:10.164239Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Short light cycles induce persistent reproductive activity in Ile-de-France rams.
34()
215-26
European breeds of rams appear to be responsive to photoperiodic changes even though there are large differences between breeds in the timing and amplitude of endocrine (LH and testosterone) and gametogenetic variations before the sexual season. Light regimens such as 6-month light cycles or alternations of constant short and long days every 12-16 weeks are able to entrain the parameters of sexual activity. In these regimens in which the period of the light cycle is shortened, LH release is markedly stimulated during decreasing daylength and evidence is presented, from the relationship of LH and testosterone patterns, that the dampening of LH stimulation could simply result from the effect of steroid feedback. However, there is a gap of several weeks between the maximum LH and testosterone concentrations during which testis growth occurs. Experiments were conducted with Ile-de-France rams, markedly seasonal breeders, in which the period of the light cycle was decreased, in different groups of animals, from 6 to 4, 3, 2 or 1 month. Rams submitted to the three light regimens with the longest periods presented testicular variations which paralleled those of the photoperiod, but those kept in the two regimens with the shortest periods had a progressive increase in testicular weight up to the maximum value (300-350 g) with no further major changes. Therefore, in rams kept in 2-month light cycles, testicular weight remained constant for twelve successive cycles (2 years). LH and testosterone plasma measurements indicated that LH was sufficiently stimulated to maintain testicular development during each decreasing daylength phase but that the stimulation was shifted before testosterone could reach levels at which feedback effects could be exerted. However, all the measures of sperm production were at values characteristic of the sexual season. Similar testicular weight maintenance was also obtained in rams submitted to a regimen in which short days (8L:16D) alternated every month with a split photoperiod interpreted as a long day (7L:8D:1L:8D). It is concluded that short light cycles are able to induce persistent reproductive activity in Ile-de-France rams, which may have practical applications in sheep production systems.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "J", "identifier": "", "initials": "J", "lastname": "Pelletier" }, { "affiliation": "", "forename": "G", "identifier": "", "initials": "G", "lastname": "Almeida" } ]
1987
3305920
D000818:Animals; D008027:Light; D007986:Luteinizing Hormone / Q000378:metabolism; D008297:Male; D012098:Reproduction; D012621:Seasons; D012756:Sheep / Q000502:physiology*; D013737:Testis / Q000033:anatomy & histology / Q000502:physiology*
D016428:Journal Article; D016454:Review
D007986:Luteinizing Hormone
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.165138Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Transgenic livestock.
34()
237-50
Single genes can now be added routinely to the genome of mice by molecular manipulation as simple Mendelian dominants; this complements the normal process of reproduction to give 'transgenic' animals. Success in ruminants is limited to a few examples in sheep and although gene expression has yet to be documented, there is every reason to expect that it will be achieved. The application of this technology to livestock improvement depends on the identification of circumstances in which the phenotype is limited by the deficiency of a single protein. While there is little evidence to indicate that single dominant genes are in general likely to have favourable effects, it is argued that there are likely to be exceptions. These include particular combinations of promoter and structural gene sequences to alter feedback control, for example through a change in tissue specificity, and the alteration of definitive proteins such as those of milk. A mouse model has been established to study the molecular manipulation of sheep milk proteins. The sheep beta lactoglobulin gene has been incorporated and the sheep whey protein is secreted by the mammary gland of transgenic mice. For the future, means to delete or reduce the expression of existing genes are likely to be important, as are more effective means of incorporation such as retroviral based methods and the incorporation of multigene constructs. The resources required to test transgenic livestock will, however, be greater than those required to create them.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "J P", "identifier": "", "initials": "JP", "lastname": "Simons" }, { "affiliation": "", "forename": "R B", "identifier": "", "initials": "RB", "lastname": "Land" } ]
1987
3305921
D000818:Animals; D001947:Breeding; D005260:Female; D005818:Genetic Engineering / Q000379:methods / Q000662:veterinary*; D007774:Lactation; D051379:Mice; D008892:Milk; D011247:Pregnancy; D012418:Ruminants / Q000235:genetics*
D016428:Journal Article; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.166779Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Use of chimaeras to study development.
34()
251-9
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "G B", "identifier": "", "initials": "GB", "lastname": "Anderson" } ]
1987
3305922
D000818:Animals; D002678:Chimera; D005314:Embryonic and Fetal Development; D005260:Female; D005315:Fetal Diseases / Q000503:physiopathology; D006824:Hybridization, Genetic; D008322:Mammals / Q000502:physiology*; D011247:Pregnancy; D012641:Selection, Genetic
D016428:Journal Article; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.167433Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Detection of early pregnancy in domestic ruminants.
34()
261-71
Tests for the detection of pregnancy early after insemination have not yet reached their full potential. Currently, the milk progesterone assay provides the earliest possible test, at an interval of one oestrous cycle after insemination, i.e. 17, 21 and 21 days in sheep, goats and cows respectively. This assay is pregnancy non-specific and rate of detection of pregnant animals is acceptable but less than desirable. Detection of activity of early pregnancy factor may develop into an excellent early test for many species, but the rosette inhibition test which is currently required has limited development and use. Pregnancy-specific protein B has been developed as a radioimmunoassay and is reliable under laboratory situations for ruminants. It can be used after 24 days of gestation in the cow. Application to field testing awaits development. Other pregnancy-associated or specific substances which are found in maternal body fluids might develop as pregnancy markers. Ultrasonic devices might provide very early detection in cattle but the expense of a test will limit application. All tests for pregnancy early after insemination have an inherent inaccuracy. Presence of an embryo at the time the test is applied will not assure pregnancy at the time of a confirmatory test, such as birth of live young or rectal examination in cows after 35 days of gestation. Therefore, no matter how early the test, a follow-up examination might be desirable in intensively managed herds or flocks. The animal industry is on the verge of new biotechnological approaches to reproductive management. The potential seems as great as the imagination.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "R G", "identifier": "", "initials": "RG", "lastname": "Sasser" }, { "affiliation": "", "forename": "C A", "identifier": "", "initials": "CA", "lastname": "Ruder" } ]
1987
3305923
D000818:Animals; D005260:Female; D011247:Pregnancy; D011257:Pregnancy Proteins / Q000097:blood; D011258:Pregnancy Tests / Q000379:methods / Q000662:veterinary*; D011270:Pregnancy, Animal / Q000378:metabolism*; D011374:Progesterone / Q000032:analysis; D012418:Ruminants / Q000502:physiology*; D014463:Ultrasonography
D016428:Journal Article; D013485:Research Support, Non-U.S. Gov't; D016454:Review
D011257:Pregnancy Proteins; D011374:Progesterone
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.169872Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Heterogeneous cell types in the corpus luteum of sheep, goats and cattle.
34()
71-85
Data on the structure, quantitation, origins and functions of the large luteal (LL) and small luteal (SL) cells of sheep, goats and cattle are reviewed. Both LL and SL cells show ultrastructural features consistent with a steroidogenic function. However, in addition to differences in size and shape, LL cells differ from SL cells primarily in possessing large numbers of secretory granules, suggesting an additional protein/polypeptide synthetic and secretory function. In sheep, morphometric estimates show that the corpus luteum (CL) contains approximately equal to 10 X 10(6) LL cells and approximately equal to 50-60 X 10(6) SL cells: individual LL cells are approximately equal to X 6 greater in volume than SL cells. During formation of the CL, granulosa and theca cells are incorporated, and evidence suggests that granulosa cells give rise to LL cells and theca cells to SL cells. However, SL cells, or cells of thecal origin, may also give rise to some LL cells. Both LL and SL cells produce progesterone in vitro. On a per cell basis, LL cells produce more progesterone than do SL cells, but SL cells show a much greater progesterone-secretory response to LH. Oxytocin is synthesized, and secreted in granule form, only by the LL cells, and relaxin, whose presence has been demonstrated convincingly only in cattle, also appears to be produced only by LL cells. The two types of luteal cell in ruminants therefore show major differences in function: the occurrence of any significant functional interaction remains to be established.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "J D", "identifier": "", "initials": "JD", "lastname": "O'Shea" } ]
1987
3305924
D000818:Animals; D002417:Cattle / Q000033:anatomy & histology*; D002454:Cell Differentiation; D003338:Corpus Luteum / Q000166:cytology*; D005260:Female; D006041:Goats / Q000033:anatomy & histology*; D008184:Luteal Cells / Q000166:cytology* / Q000378:metabolism; D008854:Microscopy, Electron; D012756:Sheep / Q000033:anatomy & histology*
D016428:Journal Article; D016454:Review
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.170424Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Luteal peptides and intercellular communication.
34()
87-99
The variety of peptides synthesized by the corpus luteum (relaxin, vasopressin, oxytocin and oxytocin-related neurophysin) and their possible intracellular effects are reviewed. After luteinization of the granulosa cells and in response to LH and FSH, the output of oxytocin is increased. In addition, insulin-like growth factor is a very potent stimulus of oxytocin secretion. Although luteal cells respond to gonadotrophins by increased production of progesterone, there is no further secretion of oxytocin. Oxytocin is localized in large luteal cells which seem not to be under the direct control of gonadotrophins. Synthesis of luteal oxytocin seems to occur during the early luteal phase according to measurements of oxytocin mRNA. Highest tissue concentrations and secretion under in-vitro conditions were observed during the mid-luteal phase, and so synthesis, storage and secretion are unlikely to occur concomitantly. Under in-vitro conditions, oxytocin is secreted concomitantly with neurophysin and progesterone, and there appears to be some form of communication between small and large luteal cells for the secretion of progesterone and oxytocin under in-vivo conditions. Evidence has been obtained that oxytocin may have local effects in the ovary by inhibition of secretion (synthesis ?) of progesterone, especially during the early luteal phase. A mechanism can be suggested whereby, under physiological conditions, oxytocin may delay the increase of progesterone by inhibition of progesterone secretion and therefore delay down regulation of its own receptor. This would prolong the life-span of the CL and the oestrous cycle. Exogenous progesterone given on Days 1-4 shortens the cycle to about 12 days. The best evidence that oxytocin may be involved in controlling luteolysis comes from immunization experiments in ewes and goats, but there is no clear evidence of this type for cattle. Basal concentrations of oxytocin at the end of the luteal phase may interact with oxytocin receptors after the inhibitory effect of progesterone in the uterus is reduced, thus initiating synthesis of PGF-2 alpha.
Journal of reproduction and fertility. Supplement
[ { "affiliation": "", "forename": "D", "identifier": "", "initials": "D", "lastname": "Schams" } ]
1987
3305925
D000818:Animals; D002417:Cattle / Q000378:metabolism*; D002450:Cell Communication; D003338:Corpus Luteum / Q000378:metabolism; D003339:Corpus Luteum Hormones / Q000378:metabolism*; D005260:Female; D010121:Oxytocin / Q000378:metabolism; D010455:Peptides / Q000378:metabolism*; D012756:Sheep / Q000378:metabolism*
D016428:Journal Article; D016454:Review
D003339:Corpus Luteum Hormones; D010455:Peptides; D010121:Oxytocin
[]
false
eng
J Reprod Fertil Suppl
0225652
0449-3087
England
[]
"2024-08-13T08:46:10.171192Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Reactivity of human trophoblast with an antibody to the HLA class II antigen, HLA-DP.
11(1)
63-70
Cytotrophoblast cells in term amniochorion and in first trimester chorionic villi were shown by immunohistology of frozen tissue sections to bind B7/21, an antibody specific for the MHC Class II antigen, HLA-DP. This binding was shown to be specific, as adsorption of the B7/21 antibody with a B cell line expressing HLA-DP prevented subsequent binding to trophoblast. When tested with a variety of other antibodies reacting with HLA-DR, HLA-DQ or the common sequences of HLA-DR, -DQ and -DP, trophoblast was negative, thus confirming previous reports. The significance of this unique pattern of reactivity of trophoblast is discussed.
Journal of reproductive immunology
[ { "affiliation": "", "forename": "P M", "identifier": "", "initials": "PM", "lastname": "Starkey" } ]
1987-05
3305926
D000911:Antibodies, Monoclonal; D005260:Female; D006681:HLA-D Antigens / Q000302:isolation & purification*; D006682:HLA-DP Antigens / Q000302:isolation & purification*; D006801:Humans; D007124:Immunoenzyme Techniques; D011247:Pregnancy; D014327:Trophoblasts / Q000276:immunology*
D016428:Journal Article
D000911:Antibodies, Monoclonal; D006681:HLA-D Antigens; D006682:HLA-DP Antigens
10.1016/0165-0378(87)90007-6
[]
false
eng
J Reprod Immunol
8001906
0165-0378
Ireland
[]
"2024-08-13T08:46:10.173157Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Frederick P. Zuspan, M.D. A festschrift.
32(7)
497-530
The Journal of reproductive medicine
[]
1987-07
3305927
D049673:History, 20th Century; D009774:Obstetrics / Q000266:history; D014481:United States
D019215:Biography; D016456:Historical Article; D016428:Journal Article; D019477:Portrait
[]
false
eng
J Reprod Med
0173343
0024-7758
United States
[]
"2024-08-13T08:46:10.173765Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Ultrasound needle guidance for amniocentesis in pregnancies with low amniotic fluid.
32(7)
513-6
In six pregnancies accompanied by oligohydramnios (three cases) or decreased amniotic fluid and maternal obesity (three cases), needles specifically designed for use with ultrasound were successfully utilized in combination with real-time ultrasound guidance for amniocentesis. There was successful fluid retrieval in all six, with two requiring more than one needle pass. All three cases accompanied by oligohydramnios later resulted in fetal death. In the three cases accompanied by decreased amniotic fluid and maternal obesity, the amniocentesis results were helpful in ensuring the existence of a normal pregnancy. A specially designed ultrasound needle used in combination with a real-time guidance system is helpful in the performance of difficult amniocentesis.
The Journal of reproductive medicine
[ { "affiliation": "", "forename": "J P", "identifier": "", "initials": "JP", "lastname": "McGahan" }, { "affiliation": "", "forename": "F", "identifier": "", "initials": "F", "lastname": "Tennant" }, { "affiliation": "", "forename": "F W", "identifier": "", "initials": "FW", "lastname": "Hanson" }, { "affiliation": "", "forename": "K K", "identifier": "", "initials": "KK", "lastname": "Lindfors" }, { "affiliation": "", "forename": "E J", "identifier": "", "initials": "EJ", "lastname": "Quilligan" } ]
1987-07
3305928
D000649:Amniocentesis / Q000379:methods*; D000653:Amniotic Fluid / Q000032:analysis; D005260:Female; D005313:Fetal Death; D006801:Humans; D011247:Pregnancy; D014463:Ultrasonography
D016428:Journal Article
[]
false
eng
J Reprod Med
0173343
0024-7758
United States
[]
"2024-08-13T08:46:10.174491Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Familial acanthosis nigricans. A longitudinal study.
32(7)
531-6
The triad of hyperandrogenism, insulin resistance and acanthosis nigricans (HAIR-AN) is known to have a familial tendency. In order to better understand the natural history and possible treatment of this disorder, we studied the clinical course of two families in which all female progeny were affected. A rapid progression of the HAIR-AN syndrome was apparent during the peripubertal period and early reproductive years. Beyond this period, the progression of HAIR-AN appeared quite variable. Rapid weight gain was a major stimulant for increasing insulin resistance and hyperandrogenemia. In the one subject with a postmenarcheal onset of the syndrome, prolonged weight reduction was associated with an improvement in the dermatologic manifestation as well as in the hyperandrogenism and insulin resistance. Oral contraceptives appear to improve the dermatologic symptoms of the HAIR-AN syndrome.
The Journal of reproductive medicine
[ { "affiliation": "", "forename": "C I", "identifier": "", "initials": "CI", "lastname": "Friedman" }, { "affiliation": "", "forename": "S", "identifier": "", "initials": "S", "lastname": "Richards" }, { "affiliation": "", "forename": "M H", "identifier": "", "initials": "MH", "lastname": "Kim" } ]
1987-07
3305929
D000052:Acanthosis Nigricans / Q000097:blood / Q000188:drug therapy / Q000235:genetics*; D000293:Adolescent; D000735:Androstenedione / Q000097:blood; D001786:Blood Glucose / Q000378:metabolism; D003276:Contraceptives, Oral / Q000627:therapeutic use; D005260:Female; D006801:Humans; D007328:Insulin / Q000097:blood; D007333:Insulin Resistance; D008137:Longitudinal Studies; D013577:Syndrome; D013739:Testosterone / Q000097:blood
D002363:Case Reports; D016428:Journal Article
D001786:Blood Glucose; D003276:Contraceptives, Oral; D007328:Insulin; D013739:Testosterone; D000735:Androstenedione
[]
false
eng
J Reprod Med
0173343
0024-7758
United States
[]
"2024-08-13T08:46:10.175512Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz
Amniotic fluid volume assessment with the four-quadrant technique at 36-42 weeks' gestation.
32(7)
540-2
An ultrasound approach was developed to identify normal amniotic fluid volume. The uterine cavity was divided into four quadrants. With the use of linear-array, real-time B-scanning, the vertical diameter of the largest pocket in each quadrant was measured. The sum of these four quadrants was used to provide a single number for the amniotic fluid volume and termed the amniotic fluid index. This approach is simple, requires little time and gives a semiquantitative estimate of amniotic fluid volume. Based on our observations, the normal amniotic fluid index in term gestation is 12.9 +/- 4.6 cm. Evaluation of the relationship between amniotic fluid volume and fetal outcome is under investigation.
The Journal of reproductive medicine
[ { "affiliation": "", "forename": "J P", "identifier": "", "initials": "JP", "lastname": "Phelan" }, { "affiliation": "", "forename": "C V", "identifier": "", "initials": "CV", "lastname": "Smith" }, { "affiliation": "", "forename": "P", "identifier": "", "initials": "P", "lastname": "Broussard" }, { "affiliation": "", "forename": "M", "identifier": "", "initials": "M", "lastname": "Small" } ]
1987-07
3305930
D000653:Amniotic Fluid; D005260:Female; D006801:Humans; D011247:Pregnancy; D011263:Pregnancy Trimester, Third; D014463:Ultrasonography / Q000379:methods*
D016428:Journal Article
[]
false
eng
J Reprod Med
0173343
0024-7758
United States
[]
"2024-08-13T08:46:10.176395Z"
https://ftp.ncbi.nlm.nih.gov/pubmed/baseline/pubmed24n0110.xml.gz