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Cynthia Gagnon
Cynthia Gagnon
Verified email at usherbrooke.ca
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Consensus-based care recommendations for adults with myotonic dystrophy type 1
T Ashizawa, C Gagnon, WJ Groh, L Gutmann, NE Johnson, G Meola, ...
Neurology: Clinical Practice 8 (6), 507-520, 2018
1592018
Predictors of disrupted social participation in myotonic dystrophy type 1
C Gagnon, J Mathieu, S Jean, L Laberge, M Perron, S Veillette, L Richer, ...
Archives of physical medicine and rehabilitation 89 (7), 1246-1255, 2008
1182008
Health supervision and anticipatory guidance in adult myotonic dystrophy type 1
C Gagnon, MC Chouinard, L Laberge, S Veillette, P Bégin, R Breton, ...
Neuromuscular Disorders 20 (12), 847-851, 2010
1022010
CpG methylation, a parent-of-origin effect for maternal-biased transmission of congenital myotonic dystrophy
L Barbé, S Lanni, A López-Castel, S Franck, C Spits, K Keymolen, ...
The American Journal of Human Genetics 100 (3), 488-505, 2017
972017
Daytime sleepiness and myotonic dystrophy
L Laberge, C Gagnon, Y Dauvilliers
Current neurology and neuroscience reports 13, 1-8, 2013
942013
207th ENMC Workshop on chronic respiratory insufficiency in myotonic dystrophies: management and implications for research, 27–29 June 2014, Naarden, The Netherlands
VA Sansone, C Gagnon
Neuromuscular Disorders 25 (5), 432-442, 2015
91*2015
Fatigue and daytime sleepiness rating scales in myotonic dystrophy: a study of reliability
L Laberge, C Gagnon, S Jean, J Mathieu
Journal of Neurology, Neurosurgery & Psychiatry 76 (10), 1403-1405, 2005
912005
Towards an integrative approach to the management of myotonic dystrophy type 1
C Gagnon, L Noreau, RT Moxley, L Laberge, S Jean, L Richer, M Perron, ...
Journal of Neurology, Neurosurgery & Psychiatry 78 (8), 800-806, 2007
902007
Evaluating the integration of chronic disease prevention and management services into primary health care
M Fortin, MC Chouinard, T Bouhali, MF Dubois, C Gagnon, M Bélanger
BMC health services research 13, 1-13, 2013
882013
Cognitive decline over time in adults with myotonic dystrophy type 1: a 9-year longitudinal study
B Gallais, C Gagnon, J Mathieu, L Richer
Neuromuscular Disorders 27 (1), 61-72, 2017
832017
Life habits in myotonic dystrophy type 1
C Gagnon, J Mathieu, L Noreau
Journal of rehabilitation medicine 39 (7), 560-566, 2007
782007
Prevalence and correlates of apathy in myotonic dystrophy type 1
B Gallais, M Montreuil, M Gargiulo, B Eymard, C Gagnon, L Laberge
BMC neurology 15, 1-8, 2015
762015
Standardized finger-nose test validity for coordination assessment in an ataxic disorder
C Gagnon, J Mathieu, J Desrosiers
Canadian journal of neurological sciences 31 (4), 484-489, 2004
642004
Clinical, psychosocial, and central correlates of quality of life in myotonic dystrophy type 1 patients
L Laberge, J Mathieu, J Auclair, É Gagnon, L Noreau, C Gagnon
European neurology 70 (5-6), 308-315, 2013
622013
Antifungal activity of Rhizobium
R Drapeau, JA Fortin, C Gagnon
Canadian Journal of Botany 51 (3), 681-682, 1973
551973
Consensus on cerebral involvement in myotonic dystrophy: workshop report: May 24–27, 2013, Ferrere (AT), Italy
E Bugiardini, G Meola
Neuromuscular Disorders 24 (5), 445-452, 2014
502014
Report of the second outcome measures in myotonic dystrophy type 1 (OMMYD-2) international workshop San Sebastian, Spain, October 16, 2013
C Gagnon, G Meola, LJ Hébert, L Laberge, M Leone, C Heatwole
Neuromuscular Disorders 25 (7), 603-616, 2015
492015
Report of the first outcome measures in myotonic dystrophy type 1 (OMMYD-1) international workshop: Clearwater, Florida, November 30, 2011
C Gagnon, G Meola, LJ Hébert, J Puymirat, L Laberge, M Leone
Neuromuscular Disorders 23 (12), 1056-1068, 2013
482013
Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes
G Overend, C Légaré, J Mathieu, L Bouchard, C Gagnon, DG Monckton
Human Molecular Genetics 28 (13), 2245-2254, 2019
452019
A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1
C Gagnon, É Petitclerc, M Kierkegaard, J Mathieu, É Duchesne, LJ Hébert
Journal of neurology 265, 1698-1705, 2018
432018
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