Skeletal Muscle Channelopathies-Reference-Cited by-同舟云学术

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Skeletal Muscle Channelopathies

Published:2020-08 Issue:3 Volume:38 Page:481-491
ISSN:0733-8619
Container-title:Neurologic Clinics
language:en
Short-container-title:Neurologic Clinics

Author:

Vivekanandam Vinojini,Munot Pinki,Hanna Michael G.,Matthews Emma

Funder

National Institute for Health Research Biomedical Research Centres

Medical Research Council

UCLH Biomedical Research Centre

Wellcome

Publisher

Elsevier BV

Subject

Clinical Neurology

Reference18 articles.

1. Prevalence study of genetically defined skeletal muscle channelopathies in England;Horga;Neurology,2013

2. Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene;Fontaine;Science,1990

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

4. A novel sodium channel mutation in a family with hypokalemic periodic paralysis;Bulman;Neurology,1999

5. Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features;Tawil;Ann Neurol,1994

Cited by 7 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. Disorders of Muscle;Neurology;2024-03-15

2. Prevalence of genetically confirmed skeletal muscle channelopathies in the era of next generation sequencing;Neuromuscular Disorders;2023-03

3. Blockers of Skeletal Muscle Nav1.4 Channels: From Therapy of Myotonic Syndrome to Molecular Determinants of Pharmacological Action and Back;International Journal of Molecular Sciences;2023-01-03

4. Muscle channelopathies;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023

5. Exome sequencing identifies a novel pathogenic CLCN1 mutation in an Iranian family with Myotonia Congenita: A case report;Human Gene;2022-12

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