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Élise Duchesne
Professeure titulaire
Centre de recherche du CHU de Québec - Université Laval
Contribution à la recherche
Axe de recherche de l'Université Laval :
Santé et bien-être durables
Thématiques de recherche de la Faculté de médecine :
Perte d’autonomie et réadaptation
Neurosciences et santé mentale
Santé des populations et pratiques optimales en santé
Transfert des connaissances
Domaines et intérêts de recherche du (de la) professeur(e) :
Appareil locomoteur et arthrite
- Système musculaire
- Activité locomotrice/troubles du mouvement
- Lésions musculosquelettiques et réparations
- Maladies musculaires
- Services et soins de réadaptation
Génétique humaine
Neurosciences, santé mentale et toxicomanies
Projets de recherche
- IMPACT, a supervised rehabilitation program for spastic ataxias: A rater-blinded, randomized controlled trial - Instituts de recherche en santé du Canada - Subvention Projet, chercheur principal - 2024-05-01 au 2027-03-31
- Améliorer la compréhension des maladies neuromusculaires pour contribuer au développement d'approches axées sur les données probantes - Fonds de recherche du Québec - Santé - Chercheur-boursier Juniors 1 et 2, Seniors, chercheur principal - 2024-05-01 au 2026-06-30
- Fond de démarrage - Nouveau chercheur - CHU de Québec – Université Laval – CHUL, Fondation du CHU de Québec - Fonds de démarrage, chercheur principal - 2024-05-01 au 2026-03-31
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Publications
- 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), Duchesne, E., Gagnon, C., Morin, M., Roussel, M.-P., BMC Musculoskeletal Disorders, 2019, 10.1186/s12891-019-2643-8
- Impact of Inflammation and Anti-inflammatory Modalities on Skeletal Muscle Healing: From Fundamental Research to the Clinic., Dumont NA, Dufresne SS, Duchesne E, Physical therapy, 2017, 10.1093/ptj/pzx056
- 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, Duchesne, E., Gagnon, C., Morin, M., Roussel, M.-P., BMC Musculoskeletal Disorders, 2019, 10.1186/s12891-019-2458-7
- Strength-training effectively alleviates skeletal muscle impairments in myotonic dystrophy type 1, Duchesne, E., Hébert, L.J., Roussel, M.-P., Neuromuscular Disorders, 2020, 10.1016/j.nmd.2020.02.015
- Mast cells can regulate skeletal muscle cell proliferation by multiple mechanisms., Côté CH, Roussel MP, Bouchard P, Duchesne E, Muscle & nerve, 2013, 10.1002/mus.23758
- Mast cell tryptase stimulates myoblast proliferation; a mechanism relying on protease-activated receptor-2 and cyclooxygenase-2., Côté CH, Tremblay MH, Duchesne E, BMC musculoskeletal disorders, 2011, 10.1186/1471-2474-12-235
- Inflammation-induced leukocyte accumulation in injured skeletal muscle: role of mast cells., Lapoite BM, Duchesne E, Tremblay MH, Côte CH, Muscle & nerve, 2008, 10.1002/mus.20998
- Monocyte depletion increases local proliferation of macrophage subsets after skeletal muscle injury., Duchesne E, Marsolais D, van Rooijen N, Bouchard P, Côté CH, BMC musculoskeletal disorders, 2013, 10.1186/1471-2474-14-359
- Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1, Duchesne, E., Gagnon, C., Mathieu, J., Leone, M., Fortin, A.-M., Girardin, M., Morin, M., Roussel, M.-P., BMC Research Notes, 2019, 10.1186/s13104-019-4554-z
- Validity of the Mini-BESTest in adults with myotonic dystrophy type 1, Gagnon, C., Roussel, M.-P., Côté, I., Mathieu, J., Hébert, L.J., Duchesne, E., Muscle and Nerve, 2020, 10.1002/mus.26893
- A More Efficient Transportable and Scalable System for Real-Time Activities and Exercises Recognition., Gaboury S, Duchesne E, Bouchard K, Thullier F, Plantevin V, Chapron K, Sensors (Basel, Switzerland), 2018, 10.3390/s18010268
- Inflammatory cells do not decrease the ultimate tensile strength of intact tendons in vivo and in vitro: protective role of mechanical loading., Frenette J, Côté CH, Duchesne E, Marsolais D, Journal of applied physiology (Bethesda, Md. : 1985), 2006, 10.1152/japplphysiol.00162.2006
- 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, 10.1016/j.arrct.2021.100172
- Intra-rater reliability and concurrent validity of quantified muscle testing for maximal knee extensors strength in men with myotonic dystrophy type 1, Duchesne, E., Hébert, L.J., Roussel, M.-P., Journal of Neuromuscular Diseases, 2019, 10.3233/JND-190388
- ACTI-DM1: Monitoring the activity level of people with myotonic dystrophy type 1 through activity and exercise recognition, Gaboury, S., Duchesne, E., Lavoie, M., Gagnon, C., Bouchard, K., Darsmstadt-Bélanger, H., Lessard, I., Lapointe, P., Chapron, K., IEEE Access, 2021, 10.1109/ACCESS.2021.3068877
- Transportable and scalable system for activities and exercises recognition in real-Time, Gaboury, S., Duchesne, E., Bouchard, K., Chapron, K., 2017 IEEE SmartWorld Ubiquitous Intelligence and Computing, Advanced and Trusted Computed, Scalable Computing and Communications, Cloud and Big Data Computing, Internet of People and Smart City Innovation, SmartWorld/SCALCOM/UIC/ATC/CBDCom/IOP/SCI 2017 - Conference Proceedings, 2018, 10.1109/UIC-ATC.2017.8397512
- Effects and Acceptability of an Individualized Home-Based 10-Week Training Program in Adults with Myotonic Dystrophy Type 1, Duchesne, E., Lapointe, P., Lavoie, M., Chapron, K., Bouchard, K., Gagnon, C., Gaboury, S., Lessard, I., Journal of Neuromuscular Diseases, 2021, 10.3233/jnd-200570
- 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, 10.1007/s00415-021-10533-6
- A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1., Hébert LJ, Duchesne É, Mathieu J, Kierkegaard M, Petitclerc É, Gagnon C, Journal of neurology, 2018, 10.1007/s00415-018-8898-4
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Contribution à l'enseignement aux cycles supérieurs
Étudiant(e)s dirigé(e)s*
Depuis 2009- Cécilia Légaré - Post-doctorat - En cours
- Laura Girard-Côté - Doctorat - En cours
- Marie-Pier Roussel - Maîtrise avec mémoire - 2018/01
- Amira Aoussim - Maîtrise avec mémoire - 2022/01
- Ines Mokhtari - Maîtrise avec mémoire - 2022/01
Encadrement d'étudiant(e)s
Direction de recherche dans les domaines suivants :
- Sciences cliniques et biomédicales
- Sciences de la réadaptation
En savoir plus sur les programmes
Disponibilité d'encadrement d'étudiant(e)s
Ce (cette) professeur(e) est présentement à la recherche d'étudiant(e)s.
Envoyer un courriel*Les supervisions d’étudiant(e)s de 1er cycle en
stage de recherche et de résident(e)s aux études médicales postdoctorales seront répertoriées
ultérieurement.