EDITORIAL
Published on 17 Dec 2020
Editorial: New Insights in Skeletal Muscle Channelopathies - A Rapidly Expanding Field
doi 10.3389/fneur.2020.626772
- 1,364 views
- 1 citation
- Frontiers in Neurology
- Neuromuscular Disorders and Peripheral Neuropathies
- Research Topics
- New Insights in Skeletal Muscle Channelopathies - A Rapidly Expanding Field
New Insights in Skeletal Muscle Channelopathies - A Rapidly Expanding Field
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Articles
ORIGINAL RESEARCH
Published on 04 Sep 2020
Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia
doi 10.3389/fneur.2020.01019
- 2,414 views
- 7 citations
ORIGINAL RESEARCH
Published on 29 Jul 2020
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients
doi 10.3389/fneur.2020.00646
- 5,687 views
- 11 citations
ORIGINAL RESEARCH
Published on 26 Jun 2020
Genotype-Phenotype Correlations and Characterization of Medication Use in Inherited Myotonic Disorders
doi 10.3389/fneur.2020.00593
- 3,481 views
- 13 citations
ORIGINAL RESEARCH
Published on 19 Jun 2020
Depletion of ATP Limits Membrane Excitability of Skeletal Muscle by Increasing Both ClC1-Open Probability and Membrane Conductance
doi 10.3389/fneur.2020.00541
- 4,190 views
- 13 citations
ORIGINAL RESEARCH
Published on 20 May 2020
Long-Term Safety and Usefulness of Mexiletine in a Large Cohort of Patients Affected by Non-dystrophic Myotonias
doi 10.3389/fneur.2020.00300
- 6,274 views
- 25 citations
ORIGINAL RESEARCH
Published on 29 Apr 2020
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4
doi 10.3389/fneur.2020.00255
- 4,151 views
- 6 citations
CORRECTION
Published on 20 Mar 2020
Corrigendum: Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
doi 10.3389/fneur.2020.00181
- 1,278 views
- 3 citations
ORIGINAL RESEARCH
Published on 13 Feb 2020
Myotonic Myopathy With Secondary Joint and Skeletal Anomalies From the c.2386C>G, p.L796V Mutation in SCN4A
doi 10.3389/fneur.2020.00077
- 3,026 views
- 9 citations
REVIEW
Published on 11 Feb 2020
Defective Gating and Proteostasis of Human ClC-1 Chloride Channel: Molecular Pathophysiology of Myotonia Congenita
doi 10.3389/fneur.2020.00076
- 6,598 views
- 18 citations
ORIGINAL RESEARCH
Published on 06 Feb 2020
CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita
doi 10.3389/fneur.2020.00063
- 4,251 views
- 9 citations
REVIEW
Published on 17 Jan 2020
An Up-to-Date Overview of the Complexity of Genotype-Phenotype Relationships in Myotonic Channelopathies
doi 10.3389/fneur.2019.01404
- 5,832 views
- 37 citations
