Déficits en 21-hydroxylase et infertilité féminine : de la physiopathologie à la prise en charge thérapeutique
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology,Reproductive Medicine,General Medicine
Reference30 articles.
1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000
2. Nonclassic 21-hydroxylase deficiency;Dewailly;Semin Reprod Med,2002
3. 21-hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease;Forest;Ann Endocrinol (Paris),2005
4. Congenital adrenal hyperplasia;Witchel;J Pediatr Adolesc Gynecol,2011
5. Recent advances in the diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Forest;Hum Reprod Update,2004
Cited by 5 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. Fertility and pregnancy outcomes in women with nonclassic 21‐hydroxylase deficiency;Clinical Endocrinology;2022-11-17
2. A rare case report about a congenital adrenal hyperplasia by 21-hydroxylase lock in its pure virilizing form discovered in adolescence;Annals of Medicine & Surgery;2022-06
3. Clinical outcomes and characteristics of P30L mutations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Endocrine;2020-05-05
4. Non-classic cytochrome P450 oxidoreductase deficiency strongly linked with menstrual cycle disorders and female infertility as primary manifestations;Human Reproduction;2020-04
5. Health problems of adolescent and adult patients with 21-hydroxylase deficiency;Clinical Pediatric Endocrinology;2018
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