Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lucy Magill"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Prader-Willi-Syndrome (PWS) is characterized by hypothalamic-pituitary dysfunction. Recent research suggests starting growth hormone-treatment (GHT) as soon as possible. The aim of this study is to analyze possible differences in
Externí odkaz:
https://doaj.org/article/e1728a51d61b490ab6d4c4537141ab6d
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Prader-Willi-Syndrome (PWS) is characterized by hypothalamic-pituitary dysfunction. Recent research suggests starting growth hormone-treatment (GHT) as soon as possible. The aim of this study is to analyze possible differences in auxologic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::853eb0ec7de8fccea37b4a9dbc21e76c
https://doi.org/10.1186/s13023-020-01527-0
https://doi.org/10.1186/s13023-020-01527-0
Publikováno v:
Journal of the Endocrine Society
Introduction: Prader-Willi-Syndrom (PWS) is a rare multisystem genetic disorder characterized by hypothalamic-pituitary dysfunction. Various characteristic clinical features and several endocrinological problems such as hypogonadism, hypothyroidism,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d470525492b9328eb8fd2ac0f61ecdf
http://europepmc.org/articles/PMC7209690
http://europepmc.org/articles/PMC7209690