Cynthia Gagnon

Summary

Country: Canada

Publications

  1. ncbi request reprint Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique, Jonquière, Québec G7X 7X2, Canada
    Int J Rehabil Res 27:253-6. 2004
  2. ncbi request reprint Measurement of participation in myotonic dystrophy: reliability of the LIFE-H
    Cynthia Gagnon
    Centre for Interdisciplinary Rehabilitation and Social Integration, Rehabilitation Institute of Quebec City, Que, Canada
    Neuromuscul Disord 16:262-8. 2006
  3. doi request reprint Predictors of disrupted social participation in myotonic dystrophy type 1
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique de Jonquière, Jonquière, QC, Canada
    Arch Phys Med Rehabil 89:1246-55. 2008
  4. ncbi request reprint Life habits in myotonic dystrophy type 1
    Cynthia 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
  5. doi request reprint Daytime sleepiness and myotonic dystrophy
    Luc Laberge
    ÉCOBES Recherche et Transfert, Cégep de Jonquière, 3791, rue de la fabrique, Jonquière, Quebec, Canada, G7X 7W2
    Curr Neurol Neurosci Rep 13:340. 2013
  6. ncbi request reprint Standardized finger-nose test validity for coordination assessment in an ataxic disorder
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique, Jonquière, Quebec, Canada
    Can J Neurol Sci 31:484-9. 2004
  7. ncbi request reprint Cognitive Deficits Associated with Sleep Apnea in Myotonic Dystrophy Type 1
    Benjamin Gallais
    Groupe de recherche interdisciplinaire sur les maladies neuromusculaires GRIMN, Jonquière, QC, Canada
    J Neuromuscul Dis 1:95-98. 2014
  8. ncbi request reprint Prevalence of lifestyle risk factors in myotonic dystrophy type 1
    Cynthia 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
  9. doi request reprint Clinical, psychosocial, and central correlates of quality of life in myotonic dystrophy type 1 patients
    Luc Laberge
    ÉCOBES Recherche et Transfert, Cégep de Jonquière, Quebec, Que, Canada
    Eur Neurol 70:308-15. 2013
  10. pmc Towards an integrative approach to the management of myotonic dystrophy type 1
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique de Jonquière, Jonquière, Quebec, Canada
    J Neurol Neurosurg Psychiatry 78:800-6. 2007

Collaborators

Detail Information

Publications11

  1. ncbi request reprint Autosomal recessive spastic ataxia of Charlevoix-Saguenay: upper extremity aptitudes, functional independence and social participation
    Cynthia 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...
  2. ncbi request reprint Measurement of participation in myotonic dystrophy: reliability of the LIFE-H
    Cynthia 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...
  3. doi request reprint Predictors of disrupted social participation in myotonic dystrophy type 1
    Cynthia 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)...
  4. ncbi request reprint Life habits in myotonic dystrophy type 1
    Cynthia 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...
  5. doi request reprint Daytime sleepiness and myotonic dystrophy
    Luc Laberge
    ÉCOBES Recherche et Transfert, Cégep de Jonquière, 3791, rue de la fabrique, Jonquière, Quebec, Canada, G7X 7W2
    Curr Neurol Neurosci Rep 13:340. 2013
    ....
  6. ncbi request reprint Standardized finger-nose test validity for coordination assessment in an ataxic disorder
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique, Jonquière, Quebec, Canada
    Can J Neurol Sci 31:484-9. 2004
    ..This study explored the convergent and discriminant construct validity of the Standardized Finger-Nose Test (SFNT) in a neuromuscular disorder with ataxic features...
  7. ncbi request reprint Cognitive Deficits Associated with Sleep Apnea in Myotonic Dystrophy Type 1
    Benjamin Gallais
    Groupe de recherche interdisciplinaire sur les maladies neuromusculaires GRIMN, Jonquière, QC, Canada
    J Neuromuscul Dis 1:95-98. 2014
    ..Results suggest a potential role for nighttime breathing problems in the cognitive impairment often observed in DM1 patients...
  8. ncbi request reprint Prevalence of lifestyle risk factors in myotonic dystrophy type 1
    Cynthia 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...
  9. doi request reprint Clinical, psychosocial, and central correlates of quality of life in myotonic dystrophy type 1 patients
    Luc Laberge
    ÉCOBES Recherche et Transfert, Cégep de Jonquière, Quebec, Que, Canada
    Eur Neurol 70:308-15. 2013
    ..To identify sociodemographic, clinical, and central correlates of health-related quality of life (HRQoL) in DM1 patients...
  10. pmc Towards an integrative approach to the management of myotonic dystrophy type 1
    Cynthia Gagnon
    Neuromuscular Clinic, Centre de réadaptation en déficience physique de Jonquière, Jonquière, Quebec, Canada
    J Neurol Neurosurg Psychiatry 78:800-6. 2007
  11. doi request reprint Assessing upper extremity capacity as a potential indicator of needs related to household activities for rehabilitation services in people with myotonic dystrophy type 1
    Kateri Raymond
    Faculty of Medicine and Health Sciences, Universite de Sherbrooke, 3001, 12 e Avenue Nord, Sherbrooke, QC, Canada J1H 5N4 Groupe de recherche interdisciplinaire sur les maladies neuromusculaires GRIMN, Neuromuscular Clinic, Centre de réadaptation en déficience physique de Jonquière, Centre de santé et de services sociaux de Jonquière, 2230 de l Hôpital cp 1200, Jonquière, QC, Canada G7X 7X2 Electronic address
    Neuromuscul Disord 25:522-9. 2015
    ..These criteria will assist health professionals in their attempt to refer DM1 patients to rehabilitation services at the appropriate time. ..