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Neuromuscular Disorders : NMD|April 29, 2020
Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1Marie-Pier Roussel, Luc J Hébert, Elise Duchesne
Muscle & Nerve|July 2, 2013
Mast cells can regulate skeletal muscle cell proliferation by multiple mechanismsElise Duchesne, Patrice Bouchard, Marie-Pier Roussel, et al.
Journal of Neuromuscular Diseases|July 18, 2022
Impact of a 12-week Strength Training Program on Fatigue, Daytime Sleepiness, and Apathy in Men with Myotonic Dystrophy Type 1Benjamin Gallais, Marie-Pier Roussel, Luc Laberge, et al.
Muscle & Nerve|April 22, 2020
Validity of the Mini-BESTest in adults with myotonic dystrophy type 1Elise Duchesne, Luc J Hébert, Jean Mathieu, et al.
Journal of Neuromuscular Diseases|September 11, 2023
Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1Amira Aoussim, Cécilia Légaré, Marie-Pier Roussel, et al.
Journal of Neurology|April 28, 2021
Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up studyMarie-Pier Roussel, Marie-Michèle Fiset, Laurie Gauthier, et al.
BMC Research Notes|August 21, 2019
Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1Marie-Pier Roussel, Marika Morin, Mélina Girardin, et al.
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