Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey-Reference-Cited by-同舟云学术

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Pain in SCN4A Mutated P.A1156T muscle sodium channelopathy-a postal survey

Published:2018-01-11 Issue:6 Volume:57 Page:1014-1017
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Suokas Kimmo¹,Palmio Johanna²,Sandell Satu³,Udd Bjarne²,Hietaharju Aki¹

Affiliation:

1. Department of Neurology; Tampere University Hospital; P.O. Box 2000 FI-33521 Tampere Finland

2. Neuromuscular Research Center; University Hospital of Tampere; Tampere Finland

3. Department of Neurology; Southern Ostrobothnia Hospital District; Seinäjoki Finland

Funder

Finnish Association for the Study of Pain

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference26 articles.

1. Skeletal muscle sodium channelopathies;Nicole;Curr Opin Neurol,2015

2. Genotype phenotype associations across the voltage-gated sodium channel family;Brunklaus;J Med Genet,2014

3. The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment;Matthews;Brain,2010

4. Pathomechanisms in channelopathies of skeletal muscle and brain;Cannon;Annu Rev Neurosci,2006

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

Cited by 4 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. Mouse models of non-dystrophic and dystrophic myotonia exhibit nociplastic pain-like behaviors;2024-06-22

2. Pain as a significant symptom in patients with periodic paralysis—A cross‐sectional survey;Muscle & Nerve;2021-04-05

3. Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients;Frontiers in Neurology;2020-07-29

4. Fibromyalgia and small fiber neuropathy: the plot thickens!;Clinical Rheumatology;2018-09-20

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