Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis-Reference-Cited by-同舟云学术

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Genetic variant rs623011 (17q24.3) associates with non-familial thyrotoxic and sporadic hypokalemic paralysis

Published:2012-12 Issue: Volume:414 Page:105-108
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Chu Pei-Yi,Cheng Chih-Jen,Tseng Min-Hua,Yang Sung-Sen,Chen Hsiang-Cheng,Lin Shih-Hua

Funder

Research Fund of the Tri-Service General Hospital

Teh-Tzer Study Group for the Human Medical Research Foundation

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference30 articles.

1. Laboratory tests to determine the cause of hypokalemia and paralysis;Lin;Arch Intern Med,2004

2. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis;Ptacek;Cell,1994

3. The primary periodic paralyses: diagnosis, pathogenesis and treatment;Venance;Brain,2006

4. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current;Jurkat-Rott;Proc Natl Acad Sci USA,2000

5. Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis;Matthews;Neurology,2009

Cited by 12 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. Periodic paralysis;Handbook of Clinical Neurology;2024

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

4. Thyrotoxic myopathy: research status, diagnosis, and treatment;Endokrynologia Polska;2022-01-24

5. Ion Channel Gene Mutations Causing Skeletal Muscle Disorders: Pathomechanisms and Opportunities for Therapy;Cells;2021-06-16

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