Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis-Reference-Cited by-同舟云学术

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Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis

Published:2016-03-02 Issue:13 Volume:86 Page:1190-1198
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Song I-Wen,Sung Chih-Chien,Chen Chien-Hsiun,Cheng Chih-Jen,Yang Sung-Sen,Chou Yi-Chun,Yang Jenn-Hwai,Chen Yuan-Tsong,Wu Jer-Yuarn,Lin Shih-Hua

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference38 articles.

1. Laboratory Tests to Determine the Cause of Hypokalemia and Paralysis

2. Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

3. Inward-rectifying potassium channelopathies: new insights into disorders of sodium and potassium homeostasis

4. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

5. Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome

Cited by 14 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. A single-center retrospective study on the clinical features of thyrotoxic periodic paralysis;PLOS ONE;2024-08-01

2. Atypical Normokalemic Case of Thyrotoxic Periodic Paralysis in a Pediatric Patient;Cureus;2024-04-02

3. Periodic paralysis;Handbook of Clinical Neurology;2024

4. Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan;Frontiers in Neurology;2023-01-26

5. Thyrotoxicosis Periodic Paralysis: A Rare Presentation of a Common Disease;Cureus;2022-05-31

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