Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

Purpose of developing the guidelines: The first guidelines for diagnosis and treatment of 21-hydroxylase deficiency (21-OHD) were published as a diagnostic handbook in Japan in 1989, with a focus on patients with severe disease. The “Guidelines for Treatment of Congenital Adrenal Hyperplasia (21-Hyd...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Pediatr Endocrinol
Prif Awduron: Ishii, Tomohiro, Anzo, Makoto, Adachi, Masanori, Onigata, Kazumichi, Kusuda, Satoshi, Nagasaki, Keisuke, Harada, Shohei, Horikawa, Reiko, Minagawa, Masanori, Minamitani, Kanshi, Mizuno, Haruo, Yamakami, Yuji, Fukushi, Masaru, Tajima, Toshihiro
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Japanese Society for Pediatric Endocrinology 2015
Pynciau:
Original Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4639531/
https://ncbi.nlm.nih.gov/pubmed/26594092
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.24.77
Tagiau: Ychwanegu Tag
Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

Eitemau Tebyg