Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: frequency in children with precocious pubarche and in adolescent girls with menstrual disturbances and/or hirsutism-Reference-Cited by-同舟云学术

Nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: frequency in children with precocious pubarche and in adolescent girls with menstrual disturbances and/or hirsutism

Published:1998-03 Issue:1 Volume:2 Page:1-7
ISSN:1427-4426
Container-title:Annals of Diagnostic Paediatric Pathology
language:en
Short-container-title:Ann Diagn Paed Pathol

Author:

Małunowicz Ewa M.,Ginalska-Malinowska Maria,Szypulska Maria,Romer Tomasz E.

Publisher

Springer Science and Business Media LLC

Link

http://link.springer.com/content/pdf/10.1007/s100570050001.pdf

Reference36 articles.

1. Arnaout MA (1992) Late-onset congenital adrenal hyperplasia in women with hirsutism. Eur J Clin Invest 22:651-658

2. Azziz R (1995) 21-Hydroxylase-defi-cient nonclassic adrenal hyperplasia. Endocrinologist 5:297–303

3. Azziz_R, Zacur HA (1989) 21-Hydroxylase deficiency in female hyperandrogenism: screening and diagnosis. J Clin Endocrinol Metab 69:577–584

4. Azziz R, Dewailly D, Owerbach D (1994) Nonclassic adrenal hyperplasia: current concepts. (Clinical review 56) J Clin Endocrinol Metab 78:810–815

5. Balducci R, Boscherini B, Mangiantini A, Morellini M, Toscano V (1994) Isolated precocious pubarche: an approach. J Clin Endocrinol Metab 79:582–589

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis;Clinical Endocrinology;2015-10-09