Clinical review 54: Genetics, diagnosis, and management of 21- hydroxylase deficiency-Reference-Cited by-同舟云学术

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Clinical review 54: Genetics, diagnosis, and management of 21- hydroxylase deficiency

Published:1994-02-01 Issue:2 Volume:78 Page:241-246
ISSN:0021-972X
Container-title:Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:Journal of Clinical Endocrinology & Metabolism

Author:

Miller W. L.

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Cited by 150 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. Challenges in treatment of patients with non-classic congenital adrenal hyperplasia;Frontiers in Endocrinology;2022-12-12

2. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision);CLIN PEDIATR ENDOCRI;2022

3. Differences in hormonal levels between heterozygous CYP21A2 pathogenic variant carriers, non-carriers, and females with non-classic congenital hyperplasia;Archives of Endocrinology and Metabolism;2022-03-16

4. Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision);Clinical Pediatric Endocrinology;2022

5. Genetic characterization of a large cohort of Argentine 21‐hydroxylase Deficiency;Clinical Endocrinology;2020-05-03

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