Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Émilie Petitclerc"'
Autor:
Marika Morin, Luc J. Hébert, Marc Perron, Émilie Petitclerc, Shanna-Rose Lake, Elise Duchesne
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-13 (2023)
Abstract Background Maximal isometric muscle strength (MIMS) assessment is a key component of physiotherapists’ work. Hand-held dynamometry (HHD) is a simple and quick method to obtain quantified MIMS values that have been shown to be valid, reliab
Externí odkaz:
https://doaj.org/article/4d92d32da6964cec9b787166a8bb0227
Publikováno v:
Journal of Rehabilitation Medicine, Vol 50, Iss 3, Pp 269-277 (2017)
Objective: To assess changes and responsiveness in outcome measures of mobility, balance, muscle strength and manual dexterity in adults with myotonic dystrophy type 1. Design: A 9-year longitudinal study conducted with 113 patients. Methods: The re
Externí odkaz:
https://doaj.org/article/aaf600fade7c44c290f639a299ea8cd6
Autor:
Cynthia Gagnon, Jean Mathieu, Mélanie Levasseur, Kateri Raymond, Benjamin Gallais, Luc Laberge, Louis Richer, Émilie Petitclerc
Publikováno v:
Disability and rehabilitation. 44(12)
For slowly progressive neuromuscular disease, prognostic approach and long-term monitoring of participation is a crucial part of rehabilitation services. To improve the prognostic approach, professionals must identify individuals at risk of having hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a053ffe5e29285c477f7941d005182e9
https://pubmed.ncbi.nlm.nih.gov/33135946
https://pubmed.ncbi.nlm.nih.gov/33135946
Publikováno v:
Journal of Neuromuscular Diseases. 5:215-224
BACKGROUND Although adult and late-onset DM1 phenotypes DM1 present distinct lower limb weaknesses portraits, resulting physical limitations have never been described separately for each phenotype. OBJECTIVE To characterize the lower limb weaknesses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08f896dea7f59e56e71e5ecd2b2ce23
https://doi.org/10.3233/jnd-170291
https://doi.org/10.3233/jnd-170291
Autor:
Luc J. Hébert, Cynthia Gagnon, Élise Duchesne, Marie Kierkegaard, Émilie Petitclerc, Jean Mathieu
Publikováno v:
Journal of Neurology. 265:1698-1705
Myotonic dystrophy type 1 (DM1) is a neuromuscular disorder presenting with major muscle impairments. However, few studies have addressed muscle strength progression using quantitative methods. The aims of this study were to document muscle strength
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8214d0092c97a7c7f15e9d71a888de3
https://doi.org/10.1007/s00415-018-8898-4
https://doi.org/10.1007/s00415-018-8898-4
Publikováno v:
Journal of Rehabilitation Medicine, Vol 50, Iss 3, Pp 269-277 (2017)
Objective: To assess changes and responsiveness in outcome measures of mobility, balance, muscle strength and manual dexterity in adults with myotonic dystrophy type 1. Design: A 9-year longitudinal study conducted with 113 patients. Methods: The res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb8ae47be5e62e9a12728a28d6f7d7d5
https://doaj.org/article/aaf600fade7c44c290f639a299ea8cd6
https://doaj.org/article/aaf600fade7c44c290f639a299ea8cd6
Publikováno v:
Neuromuscular Disorders. 27:153-158
Performance-based assessments of physical function are essential in people with myotonic dystrophy type 1 (DM1) to monitor disease progression and evaluate interventions. Commonly used are the six-minute walk test, the 10 m-walk test, the timed up-an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0ec0c65950da3cde7a54552d17c0712
https://doi.org/10.1016/j.nmd.2016.11.018
https://doi.org/10.1016/j.nmd.2016.11.018
Publikováno v:
Muscle & Nerve. 56:57-63
Introduction. Lower limb strength has never been characterized separately for late-onset and adult Myotonic Dystrophy Type 1 (DM1) phenotypes. Methods. The purpose was to: 1) describe and compare lower limb strength between the 2 DM1 phenotypes, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::018f420c13e9bb2fe8206d631346e9ce
https://doi.org/10.1002/mus.25451
https://doi.org/10.1002/mus.25451
Publikováno v:
Muscle & Nerve. 51:473-478
In myotonic dystrophy type 1 (DM1), leg muscle weakness is a major impairment. There are challenges to obtaining a clear portrait of muscle strength impairment. A systematic literature review was conducted on lower limb strength impairment in late-on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee7059e9b8b1e1e6ffee15d0f3202ef5
https://doi.org/10.1002/mus.24521
https://doi.org/10.1002/mus.24521
Publikováno v:
Neuromuscular Disorders. 29:S51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0736f2ad6553af23b79ef7826e08cd4
https://doi.org/10.1016/j.nmd.2019.06.062
https://doi.org/10.1016/j.nmd.2019.06.062