Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patients-Reference-Cited by-同舟云学术

Lower-extremity magnetic resonance imaging in patients with hyperkalemic periodic paralysis carrying the SCN4A mutation T704M: 30-month follow-up of seven patients

Published:2018-10 Issue:10 Volume:28 Page:837-845
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Jeong Ha-Neul,Yi Ji Sook,Lee Young Han,Lee Jung Hwan,Shin Ha Young,Choi Young-Chul^ORCID,Kim Seung Min

Funder

Yonsei University College of Medicine for 2016

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Clinical diversity of SCN4A-mutation-associated skeletal muscle sodium channelopathy;Lee;J Clin Neurol,2009

2. Identification of a mutation in the gene causing hyperkalemic periodic paralysis;Ptacek;Cell,1991

3. Correlating phenotype and genotype in the periodic paralyses;Miller;Neurology,2004

4. Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals;Charles;J Neurol,2013

5. Progressive myopathy in hyperkalemic periodic paralysis;Bradley;Arch Neurol,1990

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