Does Primary Salt Wasting Occur in 11-Beta-Hydroxylase Deficiency?
Author:
Publisher
Walter de Gruyter GmbH
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://www.degruyter.com/document/doi/10.1515/JPEM.1995.8.4.275/pdf
Reference16 articles.
1. Clinical and Biochemical Variability of Congenital Adrenal Hyperplasia Due to llβ-Hydroxylase Deficiency, A Study of 25 Patients*
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. Challenges in treatment of patients with non-classic congenital adrenal hyperplasia;Frontiers in Endocrinology;2022-12-12
2. Classical 11β-Hydroxylase Deficiency Caused by a Novel Homozygous Mutation: A Case Study and Literature Review;Cureus;2022-01-23
3. 11β-Hydroxylase Deficiency;Encyclopedia of Endocrine Diseases;2004
4. Bilateral Laparoscopic Adrenalectomy for Congenital Adrenal Hyperplasia with Severe Hypertension, Resulting from Two Novel Mutations in Splice Donor Sites of CYP11B1;The Journal of Clinical Endocrinology & Metabolism;2000-11-01
5. Combined 21-Hydroxylase and llß-Hydroxylase Deficiency: Patient Report and Molecular Basis;Journal of Pediatric Endocrinology and Metabolism;2000-01
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