Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Maurice D. Kogut"'
Autor:
S. Peleg, John Kucharczyk, M.S. Croxson, Gabriella Andraghetti, H.K. Ibbertson, H.M. Dunlop, A. Fraser, Renzo Cordera, S.R. Bloom, R. Arnon, Maurice D. Kogut, A.J. Bacarese-Hamilton, Roberto Gherzi, T.E. Adrian, Janet Lemoine, Th.C. Kamilaris, Gertrude Costin, K.J. Manolas, R. Eshet, L. Adezati, C. Fuchs, I.M. Holdaway, A. Sheehan, R.B. Welbourn, Z. Josefsberg, Zvi Laron
Publikováno v:
Hormone Research. 22:I-V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad390f5fe13f36e01963638f26c70f4b
https://doi.org/10.1159/000180102
https://doi.org/10.1159/000180102
Autor:
Maurice D. Kogut
Publikováno v:
Current Problems in Pediatrics. 4:3-59
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4d718cfc71e59c6c1cc7fcf4d4e0f33
https://doi.org/10.1016/s0045-9380(74)80039-3
https://doi.org/10.1016/s0045-9380(74)80039-3
Autor:
Maurice D. Kogut, Gertrude Costin
Publikováno v:
Hormone Research. 22:260-269
To determine the pathogenesis of carbohydrate intolerance associated with gonadal dysgenesis, plasma glucose, insulin, glucagon, and growth hormone responses to oral glucose and intravenous tolbutamide, arginine and insulin were evaluated in 21 nonob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a845ec617cfc5d18b8f2ada81d39a1
https://doi.org/10.1159/000180104
https://doi.org/10.1159/000180104
Publikováno v:
The Journal of Pediatrics. 91:728-733
Thyroid glands from 33 children with hyperthyroidism and nine with juvenile lymphocytic thyroiditis were examined histologically and for IgG, IgA, IgM, and C3 by immunofluorescent staining. There was no significant difference between glands with JLT
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e54b457c9eaeb8ed0acc38c8fd85fde
https://doi.org/10.1016/s0022-3476(77)81024-x
https://doi.org/10.1016/s0022-3476(77)81024-x
Autor:
Thomas F. Roe, Maurice D. Kogut
Publikováno v:
Pediatric Research. 11:664-669
After the infusion of fructose, 0.25 g/kg body weight, blood uric acid levels were significantly increased above the mean basal value in five patients with glycogen storage disease (GSD), type I (P less than 0.02-P less than 0.05). The mean fasting b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c2c54c0b66cceb97d8abbe3a6a8190d
https://doi.org/10.1203/00006450-197705000-00008
https://doi.org/10.1203/00006450-197705000-00008
Autor:
Harry B. Neustein, Alfred J. Pennisi, Robert B. Ettenger, Jerry A. Schneider, Maurice D. Kogut, Mohammad H. Malekzadeh, Christel H. Uittenbogaart, Richard N. Fine
Publikováno v:
The American Journal of Medicine. 63:525-533
Five children with end-stage renal disease resulting from cystinosis received seven cadaver renal allografts. Four recipients have functioning grafts eight to 55 months after receiving the transplant and one recipient lost two grafts at 17 and 26 mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dbd431c047d9327ca50d9745e3059e2
https://doi.org/10.1016/0002-9343(77)90197-8
https://doi.org/10.1016/0002-9343(77)90197-8
Publikováno v:
Pediatrics. 50:881-889
Two 8-year-old girls, one of whom had Down's syndrome, presented with myxedema and precocious sexual development. Elevated circulating thyrotrophin (TSH), luteinizing hormone (LH), follicle-stimulating hormone (FSH) levels, and prolactin activities w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9db7eb088c8bc6ceda2fa051849bd1ad
https://doi.org/10.1542/peds.50.6.881
https://doi.org/10.1542/peds.50.6.881
Publikováno v:
Biochemical Genetics. 7:73-85
The isoenzymes of hypoxanthine-guanine-phosphoribosyl transferase (HGPRT; E. C. 2.4.2.8) were studied by polyacrylamide gel disc electrophoresis in the erythrocytes of a family in which there was a partial deficiency of this X-linked enzyme. Hyperuri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b40d181e3f0faf50631c45419ad76967
https://doi.org/10.1007/bf00487011
https://doi.org/10.1007/bf00487011
Publikováno v:
The Journal of Pediatrics. 75:632-635
Although intermittent diarrhea in type I glycogen storage disease has not been emphasized previously, we have frequently observed it as a clinical manifestation in our patients. In an attempt to delineate the etiology of the diarrhea, 8 patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcbea5fa84cca98be6bcd205d1648f54
https://doi.org/10.1016/s0022-3476(69)80459-2
https://doi.org/10.1016/s0022-3476(69)80459-2
Autor:
George N. Donnell, Maurice D. Kogut
Publikováno v:
Pediatrics. 28:566-577
A 13-month-old female with ganglioneuroblastoma originating in the lower pole of the left kidney has been described. This patient had the classic findings of Cushing's syndrome, namely, moon facies, buffalo hump, hypertrichosis, acne, plethora, hyper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e18395f0986d72a0951a923f877891f
https://doi.org/10.1542/peds.28.4.566
https://doi.org/10.1542/peds.28.4.566