Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency-Reference-Cited by-同舟云学术

Long-Term Outcome of Patients With Congenital Adrenal Hyperplasia Due to 21-hydroxylase Deficiency

Published:2012-11 Issue:5 Volume:344 Page:363-373
ISSN:0002-9629
Container-title:The American Journal of the Medical Sciences
language:en
Short-container-title:The American Journal of the Medical Sciences

Author:

Mnif Mouna Feki,Kamoun Mahdi,Mnif Fatma,Charfi Nadia,Kallel Nozha,Ben Naceur Basma,Rekik Nabila,Abid Mohamed,Mnif Zainab,Sfar Mohamed Habib,Sfar Mohamed Tahar,Hachicha Mongia,Keskes Leila Ammar

Publisher

Elsevier BV

Subject

General Medicine

Reference54 articles.

1. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;White;Endocr Rev,2000

2. 21-Hydroxylase deficiency: an exemplary model of the contribution of molecular biology in the understanding and management of the disease;Forest;Ann Endocrinol,2005

3. Congenital adrenal hyperplasia in adults: a review of medical, surgical and psychological issues;Ogilvie;Clin Endocrinol,2006

4. Adrenomedullary dysplasia and hypofunction in patients with classic 21-hydroxylase deficiency;Merke;N Engl J Med,2000

5. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency—management in adults;Ambroziak;Endokrynol Pol,2010

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