Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches-Reference-Cited by-同舟云学术

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Muscle and brain sodium channelopathies: genetic causes, clinical phenotypes, and management approaches

Published:2020-07 Issue:7 Volume:4 Page:536-547
ISSN:2352-4642
Container-title:The Lancet Child & Adolescent Health
language:en
Short-container-title:The Lancet Child & Adolescent Health

Author:

Matthews Emma,Balestrini Simona,Sisodiya Sanjay M,Hanna Michael G

Funder

Wellcome Clinical Research Career Development Fellowship

Medical Research Council

Publisher

Elsevier BV

Subject

Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health

Reference105 articles.

1. Sodium channelopathies of skeletal muscle;Cannon;Handb Exp Pharmacol,2018

2. Neonatal hypotonia can be a sodium channelopathy: recognition of a new phenotype;Matthews;Neurology,2008

3. Stridor as a neonatal presentation of skeletal muscle sodium channelopathy;Matthews;Arch Neurol,2011

4. Severe neonatal non-dystrophic myotonia secondary to a novel mutation of the voltage-gated sodium channel (SCN4A) gene;Gay;Am J Med Genet A,2008

5. Severe neonatal episodic laryngospasm due to de novo SCN4A mutations: a new treatable disorder;Lion-Francois;Neurology,2010

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