Thyrotoxic Periodic Paralysis with Graves' Disease Leading to the Discovery of a Hidden Nonclassic 11β Hydroxylase Deficiency-Reference-Cited by-同舟云学术

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Thyrotoxic Periodic Paralysis with Graves' Disease Leading to the Discovery of a Hidden Nonclassic 11β Hydroxylase Deficiency

Published:2013 Issue:1 Volume:52 Page:85-88
ISSN:0918-2918
Container-title:Internal Medicine
language:en
Short-container-title:Intern. Med.

Author:

Kim Jin Hwa¹,Park Geon²,Kim Sang Yong¹,Bae Hak Yeon¹

Affiliation:

1. Department of Endocrinology and Metabolism, Chosun University Hospital, Republic of Korea

2. Department of Laboratory Medicine, Chosun University Hospital, Republic of Korea

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Link

https://www.jstage.jst.go.jp/article/internalmedicine/52/1/52_52.8032/_pdf

Cited by 6 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. Identification and functional characterization of compound heterozygous CYP11B1 gene mutations;Endocrine;2024-01-29

2. Steroid 11β-hydroxylase deficiency and related disorders;Genetic Steroid Disorders;2023

3. Congenital lipoid adrenal hyperplasia with Graves' disease: A case report;World Journal of Clinical Cases;2022-09-16

4. Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency;The Journal of Clinical Endocrinology & Metabolism;2021-04-08

5. Graves’ Thyrotoxicosis Leading to Adrenal Decompensation and Hyperandrogenemia in a Pediatric Patient with Salt-Wasting Congenital Adrenal Hyperplasia;Case Reports in Endocrinology;2018-11-22

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