Guidelines on clinical presentation and management of nondystrophic myotonias

Author:

Stunnenberg Bas C.1,LoRusso Samantha2,Arnold W. David2,Barohn Richard J.3,Cannon Stephen C.4,Fontaine Bertrand5,Griggs Robert C.6,Hanna Michael G.7,Matthews Emma7ORCID,Meola Giovanni89,Sansone Valeria A.910,Trivedi Jaya R.11,van Engelen Baziel G.M.1,Vicart Savine5,Statland Jeffrey M.3ORCID

Affiliation:

1. Department of Neurology Radboud University Medical Center Nijmegen the Netherlands

2. Department of Neurology Ohio State University Wexner Medical Center Columbus Ohio

3. Department of Neurology University of Kansas Medical Center Kansas City Kansas

4. Department of Physiology, David Geffen School of Medicine University of California Los Angeles, Los Angeles California

5. Assistance Publique‐Hôpitaix de Paris, Sorbonne Université, INSERM, Service of Neuro‐Myology and UMR 974 Institute of Myology, University Hospital Pitié‐Salpêtrière Paris France

6. Department of Neurology University of Rochester Rochester New York

7. MRC Centre for Neuromuscular Diseases, Department of Neuromuscular diseases UCL Queen Square Institute of Neurology United Kingdom

8. Department of Neurorehabilitation Sciences Casa Cura Policlinico Milan Italy

9. Department of Biomedical Sciences for Health University of Milan Milan Italy

10. Neurorehabilitation Unit, University of Milan NEuroMuscular Omnicentre (NEMO), Fondazione Serena Onlus Milan Italy

11. Department of Neurology and Neurotherapeutics UT Southwestern Medical Center Dallas Texas

Funder

Advanced Foods and Materials Canada

Publisher

Wiley

Subject

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

Reference149 articles.

1. The Skeletal Muscle Chloride Channel in Dominant and Recessive Human Myotonia

2. Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita

3. Tonische Krämpfe in willkürliche bewegten Muskeln (Myotonia congenita);Strümpell A;Berl Klin Wochenchr,1881

4. Klinischen und Pathologisch‐Anatomisches von der Thomsenschen Krankheit;Erb W;Neurol Centralblb.,1885

5. Prevalence study of genetically defined skeletal muscle channelopathies in England

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