Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Jeremy M, Kirk"'
Autor:
Jan, Idkowiak, Yasir S, Elhassan, Pascoe, Mannion, Karen, Smith, Rachel, Webster, Vrinda, Saraff, Timothy G, Barrett, Nicholas J, Shaw, Nils, Krone, Renuka P, Dias, Melanie, Kershaw, Jeremy M, Kirk, Wolfgang, Högler, Ruth E, Krone, Michael W, O'Reilly, Wiebke, Arlt
Publikováno v:
European Journal of Endocrinology
Objective Androgen excess in childhood is a common presentation and may signify sinister underlying pathology. Data describing its patterns and severity are scarce, limiting the information available for clinical decision processes. Here, we examined
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8b0a894900b51e13937e5072a75f72f1
https://pubmed.ncbi.nlm.nih.gov/30566905
https://pubmed.ncbi.nlm.nih.gov/30566905
Autor:
Silvia Parajes, Lourdes Loidi, Nicole Reisch, Vivek Dhir, Ian T. Rose, Rainer Hampel, Marcus Quinkler, Gerard S. Conway, Lidia Castro-Feijóo, David Araujo-Vilar, Manuel Pombo, Fernando Dominguez, Emma L. Williams, Trevor R. Cole, Jeremy M. Kirk, Elke Kaminsky, Gill Rumsby, Wiebke Arlt, Nils Krone
Publikováno v:
Endocrinology. 151:839-839
Context: Steroid 11β-hydroxylase (CYP11B1) deficiency (11OHD) is the second most common form of congenital adrenal hyperplasia (CAH). Cases of nonclassic 11OHD are rare compared with the incidence of nonclassic 21-hydroxylase deficiency. Objective:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf2b03c0f1bf8f45db77fe34ac21bc7
https://doi.org/10.1210/endo.151.2.9999
https://doi.org/10.1210/endo.151.2.9999