Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle Channelopathies-Reference-Cited by-同舟云学术

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Electromyographic Features in a Chinese Cohort With Hereditary Skeletal Muscle Channelopathies

Published:2020-05 Issue:3 Volume:37 Page:231-238
ISSN:0736-0258
Container-title:Journal of Clinical Neurophysiology
language:en
Short-container-title:

Author:

Sun Jian,Luo Sushan,Song Jie,Huang Jun,Cai Shuang,Zhu Wenhua,Zhou Lei,Xi Jianying,Lin Jie,Lu Jiahong,Xu Minjie,Dou Tonghai,Zhao Chongbo,Qiao Kai

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Neurology (clinical),Neurology,Physiology

Reference24 articles.

1. Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias;Platt;Curr Opin Neurol,2009

2. Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome;Plaster;Cell,2001

3. Channelopathies of skeletal muscle excitability;Cannon;Compr Physiol,2015

4. Transient paresis in myotonic syndromes. A surface EMG study;Zwarts;Brain,1989

5. Electromyography guides toward subgroups of mutations in muscle channelopathies;Fournier;Ann Neurol,2004

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. Genetic defects are common in myopathies with tubular aggregates;Annals of Clinical and Translational Neurology;2021-12-15

2. Clinical and genetic spectrum of a Chinese cohort with SCN4A gene mutations;Neuromuscular Disorders;2021-09

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