Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Brain F, Meyer"'
Autor:
Mohammad A. Alqahtani, Ayed A. Shati, Minjing Zou, Ali M. Alsuheel, Abdullah A. Alhayani, Saleh M. Al-Qahtani, Hessa M. Gilban, Brain F. Meyer, Yufei Shi
Publikováno v:
International Journal of Endocrinology, Vol 2015 (2015)
Congenital adrenal hyperplasia (CAH) due to steroid 11β-hydroxylase deficiency is the second most common form of CAH, resulting from a mutation in the CYP11B1 gene. Steroid 11β-hydroxylase deficiency results in excessive mineralcorticoids and andro
Externí odkaz:
https://doaj.org/article/f6789759e2874903a43b3c8cf939d15c
Autor:
Arif O, Khan, Mohammed A, Aldahmesh, Saeed, Al-Gehedan, Brian F, Meyer, Brain F, Meyer, Fowzan S, Alkuraya
Publikováno v:
Ophthalmic Genetics. 30:142-145
Purpose: To report corneal decompensation in 3 patients with recessive cornea plana. Methods: Retrospective case series. Results: An adult and two children (all unrelated) with clinical recessive cornea plana had gradual decrease in vision. Ophthalmi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b0944839047731a702c4edcc5a4115b
https://doi.org/10.1080/13816810902937084
https://doi.org/10.1080/13816810902937084