Zobrazeno 1 - 10
of 1 286
pro vyhledávání: '"Growth hormone therapy"'
Autor:
Nur Berna Çelik, Monique Losekoot, Emregül Işık, E. Nazlı Gönç, Ayfer Alikaşifoğlu, Nurgün Kandemir, Z. Alev Özön
Publikováno v:
JCRPE, Vol 16, Iss 4, Pp 481-488 (2024)
Insulin-like growth factor-1 (IGF-1) is the main driver of growth during prenatal life and acts through IGF-1 receptor (IGF1R). Patients with IGF1R defects exhibit variable phenotypic features. A 10.9-year-old boy presented with severe short stature,
Externí odkaz:
https://doaj.org/article/74d2e5b26f0a432fa8c3f5c851e65c15
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 5, Pp 308-315 (2024)
Purpose Short stature is the main characteristic of Turner syndrome (TS) patients and growth hormone (GH) therapy has been essential for achieving the final adult height (Ht). In the present study, the response of TS patients with different types of
Externí odkaz:
https://doaj.org/article/6b8d322db45744c1bdc219c9a6eae65b
Autor:
Willem Staels, Jean De Schepper, Marianne Becker, Philippe Lysy, Daniel Klink, Karl Logghe, Marieken den Brinker, Anne Rochtus, Bruno Lapauw, Martine Cools, Orsalia Alexopoulou, Marie Bex, Bernard Corvilain, Laurent Crenier, Christophe De Block, Julian Donckier, Robert Hilbrands, Michel Ponchon, Guy T'Sjoen, Annick Van Den Bruel, Sara Vandewalle, Brigitte Velkeniers
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Growth hormone (GH) deficiency (GHD) in children and adolescents can vary in severity and origin, with GH replacement therapy proving effective in achieving genetic target height. Optimal outcomes are seen in those treated early and with higher doses
Externí odkaz:
https://doaj.org/article/5408dcdaa3cf4b48a68e67bffee32ae3
Autor:
Sri Nikhita Chimatapu, Swathi Sethuram, Julie G. Samuels, Alexandra Klomhaus, Cassie Mintz, Martin O. Savage, Robert Rapaport
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionWe present the evolution of GHD in adolescent males with persistent growth failure, in whom the diagnosis was established after a second GH stimulation test (GST).MethodsWe performed a retrospective chart review of children who presented
Externí odkaz:
https://doaj.org/article/fd3b49df2b7449ac8f6bf7ffd9848c0c
Publikováno v:
JIMD Reports, Vol 64, Iss 5, Pp 303-311 (2023)
Abstract Glycogen storage disease Ia (GSD Ia), also known as von Gierke disease, is caused by pathogenic variants in the G6PC1 gene (OMIM 232200) which encodes glucose‐6‐phosphatase. Deficiency of glucose‐6‐phosphatase impairs the processes o
Externí odkaz:
https://doaj.org/article/49c793fbe95e407f919911603cd776fe
Autor:
Sirmen Kızılcan Çetin, Mehmet Gökhan Ramoğlu, Zeynep Şıklar, Elif Özsu, Zehra Aycan, Hasan Ercan Tutar, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 422-432 (2022)
INTRODUCTION: Cardiac involvement is common in Noonan syndrome (NS). Concerns have been raised regarding the effect of recombinant growth hormone (rGH) use on ventricular wall thickness and a possible increased risk of cardiac side effects. This stud
Externí odkaz:
https://doaj.org/article/39021e7717cf41d081fef725aa761ecd
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundComponents of the metabolic syndrome are more common in patients with Turner syndrome (TS) than in the general population. Long-term growth hormone (GH) treatment also affects the parameters of carbohydrate metabolism. Therefore, all these
Externí odkaz:
https://doaj.org/article/bf88895732f842bb8a4d2ab5cf80af2a
Akademický článek
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Autor:
W. Kaplan, E. Al Amiri, N. Attia, I. Al Basiri, I. Romany, E. Al Shehri, A. Al Twaim, S. Al Yaarubi, A. Deeb
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Children with short stature are frequently referred late to pediatric endocrinologists in the Arabian Gulf region. This is likely a contributing factor to late initiation of treatment despite current evidence suggesting that children with short statu
Externí odkaz:
https://doaj.org/article/b710a7de4e0a43c699877ef86e3c816f
Akademický článek
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