医学名词词典
文献检索
全文求助
焦点文献
我的词汇本
我要上传名词
个人中心
登录
|
注册
首页
>
按专业查询名词
> 查询PubMed相关文献
返回上一级
名词信息
中 文 名:
单纯性阻毛早发育
英 文 名:
simple premature pubarche
中文又称:
中文曾称:
名词来源:
所属专业:
内分泌科
所属类别:
疾病诊断名词
加入我的词汇本
Pubmed相关的文献
simple premature pubarche
相关文献:
Premature pubarche, ovarian hyperandrogenism, hyperinsulinism and the polycystic ovary syndrome: from a complex constellation to a simple sequence of prenatal onset.
Ibáñez L, de Zegher F, Potau N.
J Endocrinol Invest. 1998 Oct;21(9):558-66. doi: 10.1007/BF03350781.
PMID:9856410
Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche.
Kolahdouz M, Hashemipour M, Khanahmad H, Rabbani B, Salehi M, Rabbani A, Ansari A, Naseri MM.
Adv Biomed Res. 2016 Mar 16;5:33. doi: 10.4103/2277-9175.178794. eCollection 2016.
PMID:27099846
Is anti-Mullerian hormone an indicator of potential polycystic ovary syndrome in prepubertal girls with simple obesity?
Korkmaz Ö, Gökşen D, Özen S, Darcan Ş.
Turk J Pediatr. 2016;58(4):406-412. doi: 10.24953/turkjped.2016.04.010.
PMID:28276214
Adrenarche in Prader-Willi syndrome appears not related to insulin sensitivity and serum adiponectin.
Unanue N, Bazaes R, Iñiguez G, Cortés F, Avila A, Mericq V.
Horm Res. 2007;67(3):152-8. doi: 10.1159/000096742. Epub 2006 Nov 2.
PMID:17085944
Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia.
Dolzan V, Sólyom J, Fekete G, Kovács J, Rakosnikova V, Votava F, Lebl J, Pribilincova Z, Baumgartner-Parzer SM, Riedl S, Waldhauser F, Frisch H, Stopar-Obreza M, Krzisnik C, Battelino T.
Eur J Endocrinol. 2005 Jul;153(1):99-106. doi: 10.1530/eje.1.01944.
PMID:15994751
[Hirsutism and light forms of congenital adrenogenital syndrome with 21- and 11-beta hydroxylase defect].
Zachmann M.
Schweiz Med Wochenschr. 1986 Mar 29;116(13):408-12.
PMID:3486468
© Copyright 2021 鸿泰茂源 版权所有
All Rights Reserved
京ICP备11040441号-3