A New Variant of 17.ALPHA.-Hydroxylase Deficiency with Hyperaldosteronism in Two Japanese Sisters.-Reference-Cited by-同舟云学术

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A New Variant of 17.ALPHA.-Hydroxylase Deficiency with Hyperaldosteronism in Two Japanese Sisters.

Published:1989 Issue:2 Volume:36 Page:315-323
ISSN:0013-7219
Container-title:Endocrinologia Japonica
language:en
Short-container-title:Endocrinol Japon

Author:

MONNO SATOSHI¹,TAKASU NOBUYUKI¹

Affiliation:

1. Deparment of Internal Medicine, School of Medicine, Shinshu University

Publisher

Japan Endocrine Society

Subject

General Engineering,Endocrinology

Link

http://www.jstage.jst.go.jp/article/endocrj1954/36/2/36_2_315/_pdf

Cited by 9 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. Two Cases with 17-alpha Hydroxylase Deficiency Misdiagnosed as Primary Aldosteronism;Endocrine, Metabolic & Immune Disorders - Drug Targets;2023-09-07

2. Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report;Journal of Medical Case Reports;2019-07-30

3. Congenital adrenal hyperplasia causing hypertension: an illustrative review;Journal of Human Hypertension;2017-12-18

4. 17α-hydroxylase Deficiency Mimicking Hyperaldosteronism by Aldosterone-producing Adrenal Adenoma;The Korean Journal of Medicine;2016-10-01

5. A rare cause of hypertension in a healthy 2-year-old female: Answers;Pediatric Nephrology;2012-04-26

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