21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency-Reference-Cited by-同舟云学术

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21-Hydroxylase Deficiency Transiently Mimicking Combined 21- and 11β-Hydroxylase Deficiency

Published:2008-01 Issue:5 Volume:21 Page:
ISSN:2191-0251
Container-title:Journal of Pediatric Endocrinology and Metabolism
language:
Short-container-title:

Author:

Tonetto-Fernandes V.,Lemos-Marini S.H.V.,De Mello M.P.,Ribeiro-Neto L.M.,Kater C.E.

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.2008.21.5.487/pdf

Reference24 articles.

1. Clinical and Biochemical Variability of Congenital Adrenal Hyperplasia Due to llβ-Hydroxylase Deficiency, A Study of 25 Patients*

2. Plasma 21-deoxycortisol: comparison of a time-resolved fluoroimmunoassay using a biotinylated tracer with a radioimmunossay using 125iodine

3. A CASE OF ADRENOGENITAL SYNDROME WITH ABERRANT 11β-HYDROXYLATION

4. RAPID ASSAY OF PLASMA 21-DEOXYCORTISOL AND 11-DEOXYCORTISOLIN CONGENITAL ADRENAL HYPERPLASIA

Cited by 2 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. Steroidogenesis of Corticosteroids, Genetic Mutation, and Endocrine Disruption Leading to Adrenal Insufficiency;Cortisol - Between Physiology and Pathology [Working Title];2023-11-13

2. Dual Heterozygous Mutations in CYP21A2 and CYP11B1 in a Case of Nonclassic Congenital Adrenal Hyperplasia;AACE Clinical Case Reports;2022-11

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