Výsledky vyhledávání - "Jean-Michel Marie Maurice Dubuis"

Natural History of Growth Hormone Deficiency in a Pediatric Cohort

Autor: Mohamed Faouzi, Andrew A. Dwyer, Gérald Theintz, Jean-Michel Marie Maurice Dubuis, Eglantine Elowe-Gruau, Sophie Stoppa-Vaucher, Franziska Phan-Hug, Eva Deillon, Michael Hauschild, Nelly Pitteloud, Primus-Eugen Mullis

Publikováno v: Deillon, Eva; Hauschild, Michael; Faouzi, Mohamed; Stoppa-Vaucher, Sophie; Elowe-Gruau, Eglantine; Dwyer, Andrew; Theintz, Gerald E; Dubuis, Jean-Michel; Mullis, Primus-Eugen; Pitteloud, Nelly; Phan-Hug, Franziska (2015). Natural history of growth hormone deficiency in a pediatric cohort. Hormone research in paediatrics, 83(4), pp. 252-261. Karger 10.1159/000369392

Background/Aims: Controversies still exist regarding the evaluation of growth hormone deficiency (GHD) in childhood at the end of growth. The aim of this study was to describe the natural history of GHD in a pediatric cohort. Methods: This is a retro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d9c283316b881908c4aa9aeff991ef0
https://doi.org/10.1159/000369392

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Psychological Evaluation of Young Women after Medical Treatment for Central Precocious Puberty

Autor: Jean-Michel Marie Maurice Dubuis, Renata Wetterwald, DA Baumann, EA Werder, Markus A. Landolt, P C Sizonenko

Publikováno v: Hormone Research in Paediatrics, Vol. 56, No 1-2 (2001) pp. 45-50

Objective: This study aimed at the evaluation of the subjective experience and long-term behavioral and psychological effects of precocious puberty (PP). Methods: 19 female patients who had been treated with GnRH agonists participated in a semistruct

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b25265fbeadb1c37e130f050639d5568
https://doi.org/10.1159/000048089

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Transcription factors as regulators of steroidogenic P-450 enzymes

Autor: M Peter, Jean-Michel Marie Maurice Dubuis

Publikováno v: European Journal of Clinical Investigation. 30:14-20

Steroid hormones are essential for normal sexual development, accommodation to stress, and regulation of fluid and electrolyte balance. Biosynthesis of these different classes of steroids and its appropriate regulation requires the precisely controll

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::945d555b9e265c2ef54a6b5580daf13a
https://doi.org/10.1046/j.1365-2362.2000.0300s3014.x

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Severe congenital hyperinsulinism caused by a mutation in the Kir6.2 subunit of the adenosine triphosphate-sensitive potassium channel impairing trafficking and function

Autor: Victor Bancila, Yukio Tanizawa, Eric Marthinet, Yoshimoto Oka, Jean-Michel Marie Maurice Dubuis, Valerie M. Schwitzgebel, Jacques Philippe, Alain Bloc, Bernhard Wehrle-Haller

Publikováno v: Journal of Clinical Endocrinology and Metabolism, Vol. 90, No 9 (2005) pp. 5401-6

The ATP-sensitive potassium (K(ATP)) channel, assembled from the inwardly rectifying potassium channel Kir6.2 and the sulfonylurea receptor 1, regulates insulin secretion in beta-cells. A loss of function of K(ATP) channels causes depolarization of b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc150f50cd1407ac55cbd9f83c049a9d
https://archive-ouverte.unige.ch/unige:36659

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Acute symptomatic hyponatremia and cerebral salt wasting after head injury: an important clinical entity

Autor: Jean-Michel Marie Maurice Dubuis, Petra C.M. Donati-Genet, Peter C. Rimensberger, Eric Girardin

Publikováno v: Journal of Pediatric Surgery, Vol. 36, No 7 (2001) pp. 1094-7

Hyponatremia is a well known complication of traumatic and nontraumatic cerebral injury, often related to the syndrome of inappropriate antidiuretic hormone secretion (SIADH). Nonetheless, it also can be associated with a different entity, the syndro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6128f751bef084754d51f2ed6e7aafef
https://archive-ouverte.unige.ch/unige:72737

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Disorders of the aldosterone synthase and steroid 11beta-hydroxylase deficiencies

Autor: WG Sippell, M Peter, Jean-Michel Marie Maurice Dubuis

Publikováno v: Hormone research. 51(5)

The most potent corticosteroids are 11beta-hydroxylated compounds. In humans, two cytochrome P450 isoenzymes with 11beta-hydroxylase activity, catalysing the biosynthesis of cortisol and aldosterone, are present in the adrenal cortex. CYP11B1, the ge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6930e145025bb15ec09bde63eb5aa9f
https://pubmed.ncbi.nlm.nih.gov/10559665

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Should we monitor more closely the dosage of 9 alpha-fluorohydrocortisone in salt-losing congenital adrenal hyperplasia?

Autor: P C Sizonenko, Jean-Michel Marie Maurice Dubuis, L A Lopes, Michel B. Vallotton

Publikováno v: Journal of Pediatric Endocrinology and Metabolism, Vol. 11, No 6 (1998) pp. 733-7

In salt-losing congenital adrenal hyperplasia (CAH), continuous therapy with glucocorticoids and 9 alpha-fluorohydrocortisone (9 alpha-F) remains the golden rule. Previous reports showed a growth promoting effect of 9 alpha-F therapy. In addition, 9

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117ff658d735f5ee730c72bc20f2c41b
https://pubmed.ncbi.nlm.nih.gov/9829228

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