Research Topics
| Cynthia GagnonSummaryCountry: Canada Publications
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Detail Information
Publications
Standardized finger-nose test validity for coordination assessment in an ataxic disorderCynthia Gagnon
Neuromuscular Clinic, , , , Canada
Can J Neurol Sci 31:484-9. 2004..CONCLUSION: This study demonstrated the convergent and discriminant construct validity of the SFNT in a neuromuscular disorder with ataxic features...
The potential of disease management for neuromuscular hereditary disordersMaud Christine Chouinard
Universite du Quebec a Chicoutimi, Quebec, Canada
Rehabil Nurs 34:118-26. 2009..It is believed to have the potential to significantly improve healthcare management for neuromuscular hereditary disorders and will prove useful to nurses delivering and organizing services for this population...
Towards an integrative approach to the management of myotonic dystrophy type 1Cynthia Gagnon
Neuromuscular Clinic, , , , Canada
J Neurol Neurosurg Psychiatry 78:800-6. 2007
Life habits in myotonic dystrophy type 1Cynthia Gagnon
Centre de réadaptation en déficience physique de Jonquière, 2230 de l Hôpital, CP 1200, Jonquière, Quebec, Canada
J Rehabil Med 39:560-6. 2007..To describe and compare life habits between individuals with adult and mild phenotypes of myotonic dystrophy; identify life habit dimensions in which accomplishment is compromised; and describe satisfaction related to life habits...
Predictors of disrupted social participation in myotonic dystrophy type 1Cynthia Gagnon
Neuromuscular Clinic, Centre de réadaptation en déficience physique de Jonquière, Jonquière, QC, Canada
Arch Phys Med Rehabil 89:1246-55. 2008..To identify personal and environmental predictors of the most disrupted participation domains in people with myotonic dystrophy type 1 (DM1)...
Prevalence of lifestyle risk factors in myotonic dystrophy type 1Cynthia Gagnon
Faculty of Medicine and Health Sciences, Universite de Sherbrooke, Groupe de recherche interdisciplinaire sur les maladies neuromusculaires GRIMN, Neuromuscular Clinic, Centre de santé et de services sociaux de Jonquière, Quebec, Canada
Can J Neurol Sci 40:42-7. 2013..The objectives are: 1) To determine the prevalence of risk factors among individuals with DM1; 2) To compare the prevalence among classic and mild phenotypes...
[Analysis of the nursing role in the care of patients with neuromuscular disorders]Cynthia Gagnon
Faculté de médecine et des sciences de la santé de l Université de Sherbrooke, Quebec, Canada
Can J Neurosci Nurs 32:22-9. 2010..The present evaluation process was geared toward defining nursing role in relation to systematic follow-up of neuromuscular disorders and to assess its theoretical background...
Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participationCynthia Gagnon
Neuromuscular Clinic, Centre de réadaptation en déficience physique, Jonquière, Québec G7X 7X2, Canada
Int J Rehabil Res 27:253-6. 2004..Functional independence and social participation showed a decrease performance later on and a high level of variability...
Measurement of participation in myotonic dystrophy: reliability of the LIFE-HCynthia Gagnon
Centre for Interdisciplinary Rehabilitation and Social Integration, Rehabilitation Institute of Quebec City, Que, Canada
Neuromuscul Disord 16:262-8. 2006..The LIFE-H, a measure of person-perceived social participation, demonstrates adequate test-retest and inter-rater reliability for clinical and research purposes in myotonic dystrophy...
