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Retricted access

Research article

First published 2018-7-22

Beyond the muscular involvement in non-dystrophic myotonias: The emerging role of neuromodulation

Simona Portaro, Antonino Naro, Alessia Bramanti [...]

Restorative Neurology and Neuroscience

Open access

Review article

First published 2021

Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine

Jean-François Desaphy, Concetta Altamura, Savine Vicart [...]

Journal of Neuromuscular Diseases

Retricted access

Case report

First published 2020-12

A case of paramyotonia congenita in pregnancy

EK Brooks, D Schweitzer, HL Robinson

Obstetric Medicine

Open access

Research article

First published 2024-04-30

A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel Myotonia

Carmen Campanale, Paola Laghetti, Ilaria Saltarella [...]

Journal of Neuromuscular Diseases

Open access

Research article

First published 2024-03-05

Expert Insights from a Delphi-driven Neurologists’ Panel: Real-world Mexiletine use in Patients with Myotonic Disorders in Italy

Dario Lidonnici, Pietro Brambilla, Roberto Ravasio [...]

Journal of Neuromuscular Diseases

Free access

Case report

First published 2020

Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review

Tomoya Taminato, Madoka Mori-Yoshimura, Jun Miki [...]

Journal of Neuromuscular Diseases

Retricted access

Research article

First published 1997-8

MRI Findings and Evoked Potentials in Patients with Myotonic Dystrophy versus Facioscapulohumeral Dystrophy

L. Manfrè, A. Banco, M. Midiri [...]

The Neuroradiology Journal

Search results

Beyond the muscular involvement in non-dystrophic myotonias: The emerging role of neuromodulation

Targeted Therapies for Skeletal Muscle Ion Channelopathies: Systematic Review and Steps Towards Precision Medicine

A case of paramyotonia congenita in pregnancy

A c.1775C > T Point Mutation of Sodium Channel Alfa Subunit Gene (SCN4A) in a Three-Generation Sardinian Family with Sodium Channel Myotonia

Expert Insights from a Delphi-driven Neurologists’ Panel: Real-world Mexiletine use in Patients with Myotonic Disorders in Italy

Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review

MRI Findings and Evoked Potentials in Patients with Myotonic Dystrophy versus Facioscapulohumeral Dystrophy