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Hôpital de Jonquière

Alternate name: Jonquière Hospital
ROR: 03t2rer78
OpenAlex ID: I4405275550
Measuring participation in children with disabilities using the Assessment of Life Habits
2007 · Luc Noreau, Céline Lepage, et al. · Developmental Medicine & Child Neurology · 175
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Predictors of Disrupted Social Participation in Myotonic Dystrophy Type 1
2008 · Cynthia Gagnon, Jean Mathieu, et al. · Archives of Physical Medicine and Rehabilitation · 104
Health supervision and anticipatory guidance in adult myotonic dystrophy type 1
2010 · C. Gagnon, M.C. Chouinard, et al. · Neuromuscular Disorders · 95
Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: To lump or split?
2009 · Luc Laberge, Yves Dauvilliers, et al. · Neuromuscular Disorders · 81
Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer
2006 · Jacques Simard, Martine Dumont, et al. · Journal of Medical Genetics · 81
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Epidemiological surveillance of myotonic dystrophy type 1: A 25-year population-based study
2012 · Jean Mathieu, Claude Prévost · Neuromuscular Disorders · 77
Towards an integrative approach to the management of myotonic dystrophy type 1
2007 · C. Gagnon, L. Noreau, et al. · Journal of Neurology Neurosurgery & Psychiatry · 62
Clinical, Psychosocial, and Central Correlates of Quality of Life in Myotonic Dystrophy Type 1 Patients
2013 · Luc Laberge, Jean Mathieu, et al. · European Neurology · 61
Life habits in myotonic dystrophy type 1
2007 · C Gagnon, J Mathieu, et al. · Acta Dermato Venereologica · 58
The correlation of CTG repeat length with material and social deprivation in myotonic dystrophy
2006 · L Laberge, S Veillette, et al. · Clinical Genetics · 58
Quantitative Motor Assessment in Myotonic Dystrophy
2003 · J. Mathieu, H. Boivin, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 58
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Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing
2016 · Sébastien Lévesque, Christiane Auray-Blais, et al. · Orphanet Journal of Rare Diseases · 57
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A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1
2018 · Cynthia Gagnon, Émilie Petitclerc, et al. · Journal of Neurology · 55
Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians
2008 · Nicolas Dupré, Nicolas Chrestian, et al. · Neuromuscular Disorders · 55
No Evidence of BRCA1/2 Genomic Rearrangements in High-Risk French-Canadian Breast/Ovarian Cancer Families
2006 · Anne-Marie Moisan, Jessyka Fortin, et al. · Genetic Testing · 53
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Further evidence for the reliability and validity of the Fatigue and Daytime Sleepiness Scale
2017 · Benjamin Gallais, Cynthia Gagnon, et al. · Journal of the Neurological Sciences · 48
Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster
2008 · Isabelle Gosselin, Isabelle Thiffault, et al. · Neuromuscular Disorders · 42
A 9-year follow-up study of the natural progression of upper limb performance in myotonic dystrophy type 1: A similar decline for phenotypes but not for gender
2017 · Kateri Raymond, Mélanie Levasseur, et al. · Neuromuscular Disorders · 40
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Anticipation in myotonic dystrophy type 1 parents with small CTG expansions
2015 · Annabelle Pratte, Claude Prévost, et al. · American Journal of Medical Genetics Part A · 37
Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1)
2014 · Stéphane Jean, Louis Richer, et al. · Orphanet Journal of Rare Diseases · 37
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From motor performance to participation: a quantitative descriptive study in adults with autosomal recessive spastic ataxia of Charlevoix-Saguenay
2018 · Cynthia Gagnon, Bernard Brais, et al. · Orphanet Journal of Rare Diseases · 32
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Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS)
2018 · Adam P. Vogel, Natalie Rommel, et al. · Journal of Neurology · 32
The Virtual Peg Insertion Test as an assessment of upper limb coordination in ARSACS patients: A pilot study
2014 · Cynthia Gagnon, Caroline Lavoie, et al. · Journal of the Neurological Sciences · 30
Psychological characteristics of patients with myotonic dystrophy type 1
2014 · J. A. Bertrand, S. Jean, et al. · Acta Neurologica Scandinavica · 27
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Efficacy and Tolerability of a 20-mg Dose of Methylphenidate for the Treatment of Daytime Sleepiness in Adult Patients With Myotonic Dystrophy Type 1: A 2-Center, Randomized, Double-Blind, Placebo-Controlled, 3-Week Crossover Trial
2012 · Jack Puymirat, Jean-Pierre Bouchard, et al. · Clinical Therapeutics · 25
Works count: 71
Citation count: 3,695
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