Cynthia Gagnon

Summary

Country: Canada

Publications

  1. 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
  2. ncbi request reprint The potential of disease management for neuromuscular hereditary disorders
    Maud Christine Chouinard
    Universite du Quebec a Chicoutimi, Quebec, Canada
    Rehabil Nurs 34:118-26. 2009
  3. 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
  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 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
  6. 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
  7. 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
  8. ncbi request reprint [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
  9. 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
  10. pmc Effect of rehabilitation length of stay on outcomes in individuals with traumatic brain injury or spinal cord injury: a systematic review protocol
    Marie Eve Lamontagne
    Center for Interdisciplinary Research in Rehabilitation and Social Integration, Institut de Réadaptation en Déficience Physique de Québec, 525 Boul Wilfrid Hamel, Quebec, QC G1M 2S8, Canada
    Syst Rev 2:59. 2013

Detail Information

Publications12

  1. 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...
  2. ncbi request reprint The potential of disease management for neuromuscular hereditary disorders
    Maud 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...
  3. 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
  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 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)...
  6. 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...
  7. 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
    ....
  8. ncbi request reprint [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...
  9. 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...
  10. pmc Effect of rehabilitation length of stay on outcomes in individuals with traumatic brain injury or spinal cord injury: a systematic review protocol
    Marie Eve Lamontagne
    Center for Interdisciplinary Research in Rehabilitation and Social Integration, Institut de Réadaptation en Déficience Physique de Québec, 525 Boul Wilfrid Hamel, Quebec, QC G1M 2S8, Canada
    Syst Rev 2:59. 2013
    ..However, to date no systematic review of this evidence has been performed. This makes it difficult for managers and clinicians to base their rehabilitation practices upon evidence...
  11. pmc Evaluating the integration of chronic disease prevention and management services into primary health care
    Martin Fortin
    Département de Médecine de Famille, Universite de Sherbrooke, Quebec, Canada
    BMC Health Serv Res 13:132. 2013
    ..The objective of this study is to evaluate the adaptation and implementation of an intervention involving the integration of chronic disease prevention and management (CDPM) services into primary health care...
  12. 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...