PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome-Reference-Cited by-同舟云学术

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PET evidence of cerebellar hypometabolism in a patient with familial episodic ataxia-myokymia syndrome

Published:2008-07-30 Issue:10 Volume:23 Page:1483-1485
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Kim Joong-Seok,An Jae-Young,Lee Kwang-Soo,Chung Yong-An,Choi Jin-Soo,Lee Kwon-Haeng

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference10 articles.

1. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat Genet,1994

2. Identification of two new KCNA1 mutations in episodic ataxia/myokymia families;Browne;Hum Mol Genet,1995

3. Episodic ataxia type 1: a neuronal potassium channelopathy;Rajakulendran;Neurotherapeutics,2007

4. Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia;Kinali;Neuromuscul Disord,2004

5. Episodic ataxia type 2;Strupp;Neurotherapeutics,2007

Cited by 3 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. Metabolic aspects of genetic ion channel epilepsies;Journal of Neurochemistry;2023-08-18

2. kcna1a mutant zebrafish model episodic ataxia type 1 (EA1) with epilepsy and show response to first‐line therapy carbamazepine;Epilepsia;2023-06-04

3. kcna1a mutant zebrafish as a model of episodic ataxia type 1 and epilepsy;2022-09-30

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