Episodic Ataxias: Clinical and Genetic Features-Reference-Cited by-同舟云学术

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Episodic Ataxias: Clinical and Genetic Features

Published:2016-09-25 Issue:3 Volume:9 Page:129-135
ISSN:2005-940X
Container-title:Journal of Movement Disorders
language:en
Short-container-title:JMD

Author:

Choi Kwang-Dong,Choi Jae-Hwan

Funder

National Research Foundation of Korea

Ministry of Education

Publisher

The Korean Movement Disorder Society

Subject

Clinical Neurology,Neurology

Link

http://e-jmd.org/upload/jmd-16028.pdf

Reference33 articles.

1. Primary episodic ataxias: diagnosis, pathogenesis and treatment

2. Clinical neurophysiology of the episodic ataxias: Insights into ion channel dysfunction in vivo

3. Coding and Noncoding Variation of the Human Calcium-Channel β4-Subunit Gene CACNB4 in Patients with Idiopathic Generalized Epilepsy and Episodic Ataxia

4. Mutation in the glutamate transporter EAAT1 causes episodic ataxia, hemiplegia, and seizures

5. Episodic Ataxia Associated With EAAT1 Mutation C186S Affecting Glutamate Reuptake

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