Zobrazeno 1 - 2
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pro vyhledávání: '"Christine Derycke"'
Autor:
Hilde Dotremont, Annick France, Claudine Heinrichs, Sylvie Tenoutasse, Cécile Brachet, Martine Cools, Kathleen De Waele, Guy Massa, Marie-Christine Lebrethon, Inge Gies, Jesse Van Besien, Christine Derycke, Mathieu Ziraldo, Jean De Schepper, Véronique Beauloye, Stijn Verhulst, Raoul Rooman, Marieke den Brinker
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectivesTo improve adult height in pubertal girls with a poor height prediction, treatment with growth hormone (GH) can be used in combination with a gonadotropin releasing hormone agonist (GnRHa), to delay closure of the growth plates. However, th
Externí odkaz:
https://doaj.org/article/8843aea4574f41088746d0337037a8b3
High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome
Autor:
Christine Derycke, Francis Zech, Ricard Nergårdh, Gwenaelle Diene, Maithé Tauber, Patrick Delhanty, Anita C. S. Hokken-Koelega, Sandy Faye, Renske Kuppens, Coralie Winandy, Dominique Beckers, Berthold P. Hauffa, Isabelle Kieffer, Catherine Molinas, Véronique Beauloye
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol. 11, no. 1, p. 56 [1-8] (2016)
Orphanet Journal of Rare Diseases, 11. BioMed Central Ltd.
Orphanet Journal of Rare Diseases, Vol. 11, no. 1, p. 56 [1-8] (2016)
Orphanet Journal of Rare Diseases, 11. BioMed Central Ltd.
Background Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder with different nutritional phases from suckling deficit with failure to thrive to early onset of obesity. Hyperghrelinemia has been described in PWS long before the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7efe885605638a5becae247e65fdfc40