Zobrazeno 1 - 10 of 53 pro vyhledávání: '"James B. Sidbury"'
1
Mutations in the Glucose-6-Phosphatase Gene that Cause Glycogen Storage Disease Type 1a
Autor: Janice Yang Chou, James B. Sidbury, Ke-Jian Lei, L. L. Shelly, Chi-Jiunn Pan
Publikováno v: Science. 262:580-583
Glycogen storage disease (GSD) type 1a is caused by the deficiency of D-glucose-6-phosphatase (G6Pase), the key enzyme in glucose homeostasis. Despite both a high incidence and morbidity, the molecular mechanisms underlying this deficiency have elude
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9493f93654cc23bb40a64f5a8bbb7ec
https://doi.org/10.1126/science.8211187
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2
Stable Isotopic Measurement of Endogenous Fecal Calcium Excretion in Children
Autor: James B. Sidbury, Nancy E. Vieira, Steven A. Abrams, Nora V. Esteban, Joseph Muenzer, Alfred L. Yergey
Publikováno v: Journal of Pediatric Gastroenterology and Nutrition. 12:469-473
Using a stable isotopic technique in which 42Ca was administered via a bolus injection, we measured endogenous fecal calcium excretion, Vf, in five healthy children, aged 3-14 years. The Vf averaged 1.4 +/- 0.4 mg/kg/day, and was lower than urinary C
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee130a55888174d5325d26a7a3ceca52
https://doi.org/10.1097/00005176-199105000-00010
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3
Studies of Storage Disease Glycogens
Autor: Ernest Bueding, Margaret P. Cameron, Stanley A. Orrell, James B. Sidbury, W. J. Whelan
Publikováno v: Ciba Foundation Symposium-Control of Glycogen Metabolism ISBN: 9780470719343
Ciba Foundation Symposium-Control of Glycogen Metabolism
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4fb2c0cf05463d6a1b237f85f49ae514
https://doi.org/10.1002/9780470719343.ch28
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4
Calcium kinetics in glycogen storage disease type 1a
Autor: Steven A. Abrams, James B. Sidbury, Alfred L. Yergey, Nancy E. Vieira, R. E. Goans, George H. Weiss
Publikováno v: Calcified tissue international. 59(6)
Glycogen storage disease type 1a (Von Gierke's disease) is one of the more common glycogen storage diseases (GSD). GSD 1a patients can have severe idiopathic osteopenia, often beginning at a young age. Since calcium tracer studies offer a sensitive p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c9d9c9dccb2babad2b1df20f6ea2903
https://pubmed.ncbi.nlm.nih.gov/8939770
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5
Determination of fractional absorption of dietary calcium in humans
Autor: Joan C. Marini, Nancy E. Vieira, Steven A. Abrams, James B. Sidbury, Alfred L. Yergey, Akram Aldroubi
Publikováno v: The Journal of nutrition. 124(5)
Four dual-isotopic label methods for determining true fractional absorption of dietary calcium were compared in 23 subjects. The ratio of the integrals of oral label in a 24-h pooled urine to intravenous label in the same urine is called alpha 24h an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa5a40d594bcccdaea3529127b0c35df
https://pubmed.ncbi.nlm.nih.gov/8169659
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6
Type I glycogen storage disease: nine years of management with cornstarch
Autor: Yuan-Tsong Chen, C H Bazzarre, James B. Sidbury, Rosalind A. Coleman, M M Lee
Publikováno v: European journal of pediatrics. 152
Long-term effects of cornstarch (CS) therapy on biochemical values and physical growth in children with type I glycogen storage disease (GSD I) were compared to those of children receiving continuous nocturnal nasogastric glucose feedings (CNG). Only
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d1201f9bfa6302f592174231795a60c
https://pubmed.ncbi.nlm.nih.gov/8319727
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7
Developmental changes in calcium kinetics in children assessed using stable isotopes
Autor: Bonny Specker, Alfred L. Yergey, Steven A. Abrams, James B. Sidbury, Nora V. Esteban, Nancy E. Vieira
Publikováno v: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 7(3)
Total exchangeable calcium pool size (TEP) and bone calcium accretion rate (Vo+) were measured using stable isotopes in healthy children and young adults. 42Ca or 46Ca was given intravenously to 10 children aged 10 months to 14 years and 3 women aged
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::918d343bca6c46799916f0b2c3493740
https://pubmed.ncbi.nlm.nih.gov/1585830
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9
The Daily Profile of Plasma Melatonin in Obese and Prader-Willi Syndrome Children
Autor: James B. Sidbury, Paz Abastillas, Lawrence Tamarkin, Ann McNEMAR, Hao-Chia Chen
Publikováno v: The Journal of Clinical Endocrinology & Metabolism. 55:491-495
Daily plasma melatonin profiles were determined by RIA in exogenously obese and Prader-Willi syndrome children. The melatonin RIA was validated for use in human plasma by evaluating melatonin immunoreactivity in the resultant eluate fractions of a hi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4e3d8e8db19c5a17c9e25bbd10b28e7
https://doi.org/10.1210/jcem-55-3-491
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10
Cornstarch Therapy in Type I Glycogen-Storage Disease
Autor: Marvin Cornblath, James B. Sidbury, Yuan-Tsong Chen
Publikováno v: New England Journal of Medicine. 310:171-175
TYPE I glycogen-storage disease, an inherited absence or deficiency of glucose-6-phosphatase activity in the liver, kidney, and intestines, is associated with the accumulation of glycogen in those ...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a23f3f712b6960e6c4c5c4c28dc87bbe
https://doi.org/10.1056/nejm198401193100306
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