Gagnon C - Search Results

1

Rehabilitation needs of youth with arthrogryposis multiplex congenita: Perspectives from key stakeholders.

Elfassy C, Darsaklis VB, Snider L, Gagnon C, Hamdy R, Dahan-Oliel N. Elfassy C, et al. Among authors: gagnon c. Disabil Rehabil. 2020 Aug;42(16):2318-2324. doi: 10.1080/09638288.2018.1559364. Epub 2019 Feb 11. Disabil Rehabil. 2020. PMID: 30741031

2

Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1.

Raymond K, Levasseur M, Gallais B, Richer L, Laberge L, Petitclerc É, Mathieu J, Gagnon C. Raymond K, et al. Among authors: gagnon c. Disabil Rehabil. 2022 Jun;44(12):2615-2631. doi: 10.1080/09638288.2020.1837264. Epub 2020 Nov 2. Disabil Rehabil. 2022. PMID: 33135946

3

Validity and Reliability of Outcome Measures Assessing Dexterity, Coordination, and Upper Limb Strength in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.

Gagnon C, Lessard I, Brais B, Côté I, Lavoie C, Synofzik M, Mathieu J. Gagnon C, et al. Arch Phys Med Rehabil. 2018 Sep;99(9):1747-1754. doi: 10.1016/j.apmr.2018.01.026. Epub 2018 Feb 17. Arch Phys Med Rehabil. 2018. PMID: 29462597

4

Progressive Decline in Daily and Social Activities: A 9-year Longitudinal Study of Participation in Myotonic Dystrophy Type 1.

Raymond K, Levasseur M, Mathieu J, Gagnon C. Raymond K, et al. Among authors: gagnon c. Arch Phys Med Rehabil. 2019 Sep;100(9):1629-1639. doi: 10.1016/j.apmr.2019.01.022. Epub 2019 Mar 2. Arch Phys Med Rehabil. 2019. PMID: 30831092

5

Measurement properties of wheelchair use assessment tools in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Bourassa J, Best KL, Gagnon C, Hébert LJ, Brais B, Routhier F. Bourassa J, et al. Among authors: gagnon c. Disabil Rehabil Assist Technol. 2022 Nov;17(8):907-915. doi: 10.1080/17483107.2020.1821104. Epub 2020 Sep 26. Disabil Rehabil Assist Technol. 2022. PMID: 32981404

6

Wheelchair mobility, motor performance and participation of adult wheelchair users with ARSACS: a cross-sectional study.

Bourassa J, Routhier F, Gagnon C, Rahn C, Hébert LJ, St-Gelais R, Rodrigue X, Brais B, Best KL. Bourassa J, et al. Among authors: gagnon c. Disabil Rehabil Assist Technol. 2023 May;18(4):378-386. doi: 10.1080/17483107.2020.1858195. Epub 2020 Dec 12. Disabil Rehabil Assist Technol. 2023. PMID: 33307884

7

Cross-cultural adaptation of the SWAL-QOL and the Sydney Swallow Questionnaire (SSQ) into French-Canadian and preliminary assessment for their use in an oculopharyngeal muscular dystrophy (OPMD) population.

Côté C, Fortin J, Brais B, Youssof S, Gagnon C. Côté C, et al. Among authors: gagnon c. Qual Life Res. 2022 Jan;31(1):293-302. doi: 10.1007/s11136-021-02915-0. Epub 2021 Jul 22. Qual Life Res. 2022. PMID: 34292466

8

A psychometric validation of the motives for physical activity measure for youth with intellectual disabilities (MPAM-ID).

Maïano C, Morin AJS, Tracey D, Gagnon C, Smodis McCune V, Craven RG. Maïano C, et al. Among authors: gagnon c. Disabil Rehabil. 2022 Nov;44(22):6841-6850. doi: 10.1080/09638288.2021.1970828. Epub 2021 Sep 16. Disabil Rehabil. 2022. PMID: 34528859

9

The requirement for a disease-specific patient-reported outcome measure of dysphagia in oculopharyngeal muscular dystrophy.

Côté C, Gagnon C, Youssof S, sKurtz N, Brais B. Côté C, et al. Among authors: gagnon c. Muscle Nerve. 2019 Apr;59(4):445-450. doi: 10.1002/mus.26405. Epub 2019 Jan 11. Muscle Nerve. 2019. PMID: 30575974

10

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.

Roussel MP, Morin M, Gagnon C, Duchesne E. Roussel MP, et al. Among authors: gagnon c. BMC Musculoskelet Disord. 2019 Mar 5;20(1):101. doi: 10.1186/s12891-019-2458-7. BMC Musculoskelet Disord. 2019. PMID: 30836978 Free PMC article. Review.

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