Répertoire du corps professoral

IMPACT, a supervised rehabilitation program for spastic ataxias: A rater-blinded, randomized controlled trial
Programme: Subvention Projet
Organisme(s) subventionnaire(s): Instituts de recherche en santé du Canada
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 mai 2024 au31 mars 2027

Améliorer la compréhension des maladies neuromusculaires pour contribuer au développement d'approches axées sur les données probantes
Programme: Chercheur-boursier Juniors 1 et 2, Seniors
Organisme(s) subventionnaire(s): Fonds de recherche du Québec - Santé
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 mai 2024 au30 juin 2026

Fonds de démarrage - Nouveau chercheur
Programme: Fonds de démarrage
Organisme(s) subventionnaire(s): CHU de Québec – Université Laval – CHUL
Type de financement: Subvention
Établissement tête: Université Laval
Du 1 mai 2024 au31 mars 2026

Laura Girard-Côté, Doctorat en sciences de la réadaptation

Cécilia Légaré, Stage postdoctoral en biologie cellulaire et moléculaire

Encadrements terminés dans les 5 dernières années

Ines Mokhtari, Maîtrise en sciences cliniques et biomédicales - avec mémoire

Amira Aoussim, Maîtrise en sciences cliniques et biomédicales - avec mémoire

Publications des 5 dernières années

What is Known about Muscle Strength Reference Values for Adults Measured by Hand-Held dynamometry: A scoping Review Archives of Rehabilitation Research and Clinical Translation, 2021/12/07. DOI 10.1016/j.arrct.2021.100172

Assessment of muscular strength and functional capacity in the juvenile and adult myotonic dystrophy type 1 population: a 3-year follow-up study. Journal of neurology, 2021/04/27. DOI 10.1007/s00415-021-10533-6

Effects and Acceptability of an Individualized Home-Based 10-Week Training Program in Adults with Myotonic Dystrophy Type 1 Journal of Neuromuscular Diseases, 2021. Lessard, I., Gaboury, S., Gagnon, C., Bouchard, K., Chapron, K., Lavoie, M., Lapointe, P., Duchesne, E.. DOI 10.3233/jnd-200570

ACTI-DM1: Monitoring the activity level of people with myotonic dystrophy type 1 through activity and exercise recognition IEEE Access, 2021. Chapron, K., Lapointe, P., Lessard, I., Darsmstadt-Bélanger, H., Bouchard, K., Gagnon, C., Lavoie, M., Duchesne, E., Gaboury, S.. DOI 10.1109/ACCESS.2021.3068877

Validity of the Mini-BESTest in adults with myotonic dystrophy type 1 Muscle and Nerve, 2020. Duchesne, E., Hébert, L.J., Mathieu, J., Côté, I., Roussel, M.-P., Gagnon, C.. DOI 10.1002/mus.26893

Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1 Neuromuscular Disorders, 2020. Roussel, M.-P., Hébert, L.J., Duchesne, E.. DOI 10.1016/j.nmd.2020.02.015

What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review BMC Musculoskeletal Disorders, 2019. Roussel, M.-P., Morin, M., Gagnon, C., Duchesne, E.. DOI 10.1186/s12891-019-2458-7

Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1 BMC Research Notes, 2019. Roussel, M.-P., Morin, M., Girardin, M., Fortin, A.-M., Leone, M., Mathieu, J., Gagnon, C., Duchesne, E.. DOI 10.1186/s13104-019-4554-z

Intra-rater reliability and concurrent validity of quantified muscle testing for maximal knee extensors strength in men with myotonic dystrophy type 1 Journal of Neuromuscular Diseases, 2019. Roussel, M.-P., Hébert, L.J., Duchesne, E.. DOI 10.3233/JND-190388

Correction: What is known about the effects of exercise or training to reduce skeletal muscle impairments of patients with myotonic dystrophy type 1? A scoping review (BMC Musculoskeletal Disorders (2019) 20 (101) DOI: 10.1186/s12891-019-2458-7) BMC Musculoskeletal Disorders, 2019. Roussel, M.-P., Morin, M., Gagnon, C., Duchesne, E.. DOI 10.1186/s12891-019-2643-8