Molecular Basis of Nonclassical Steroid 21-Hydroxylase Deficiency Detected by Neonatal Mass Screening in Japan-Reference-Cited by-同舟云学术

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Molecular Basis of Nonclassical Steroid 21-Hydroxylase Deficiency Detected by Neonatal Mass Screening in Japan

Published:1997-07 Issue:7 Volume:82 Page:2350-2356
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:The Journal of Clinical Endocrinology & Metabolism

Author:

Tajima Toshihiro,Jun Nakae KENJI FUJIEDA,Toyoura Takio,Shimozawa Kazuhiko,Kusuda Satoshi,Goji Katsumi,Nagashima Teturo,Cutler Gordon B.

Publisher

The Endocrine Society

Subject

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

Cited by 26 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. Differences in Hyperandrogenism Related to Early Detection of Non-Classical Congenital Adrenal Hyperplasia on Second Newborn Screen;International Journal of Neonatal Screening;2023-09-01

2. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency;Genetic Steroid Disorders;2023

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

4. Thirty-Year Lessons from the Newborn Screening for Congenital Adrenal Hyperplasia (CAH) in Japan;International Journal of Neonatal Screening;2021-06-29

5. Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited;The Journal of Clinical Endocrinology & Metabolism;2020-08-24

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