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Jean Mathieu
Jean Mathieu
Professeur agrégé, Université de Sherbrooke
Verified email at usherbrooke.ca
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Cited by
Cited by
Year
A 10-year study of mortality in a cohort of patients with myotonic dystrophy
J Mathieu, P Allard, L Potvin, C Prevost, P Begin
Neurology 52 (8), 1658-1658, 1999
5031999
ARSACS, a spastic ataxia common in northeastern Quebec, is caused by mutations in a new gene encoding an 11.5-kb ORF
JC Engert, P Bérubé, J Mercier, C Doré, P Lepage, B Ge, JP Bouchard, ...
Nature genetics 24 (2), 120-125, 2000
4832000
Assessment of a disease-specific muscular impairment rating scale in myotonic dystrophy
J Mathieu, H Boivin, D Meunier, M Gaudreault, P Begin
Neurology 56 (3), 336-340, 2001
4172001
The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum
HC Howard, DB Mount, D Rochefort, N Byun, N Dupré, J Lu, X Fan, ...
Nature genetics 32 (3), 384-392, 2002
3072002
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion
L Montermini, A Richeter, K Morgan, CM Justice, D Julien, B Castellotti, ...
Annals of Neurology: Official Journal of the American Neurological …, 1997
3031997
Specific pathological Tau protein variants characterize Pick's disease
A Delacourte, Y Robitaille, N Sergeant, L Buée, PR Hof, A Wattez, ...
Journal of Neuropathology & Experimental Neurology 55 (2), 159-168, 1996
2781996
Measuring participation in children with disabilities using the Assessment of Life Habits
L Noreau, C Lepage, L Boissiere, R Picard, P Fougeyrollas, J Mathieu, ...
Developmental Medicine & Child Neurology 49 (9), 666-671, 2007
2062007
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans
V Bayat, I Thiffault, M Jaiswal, M Tétreault, T Donti, F Sasarman, ...
PLoS biology 10 (3), e1001288, 2012
1972012
Anesthetic and surgical complications in 219 cases of myotonic dystrophy
J Mathieu, P Allard, G Gobeil, M Girard, M De Braekeleer, P Begin
Neurology 49 (6), 1646-1650, 1997
1961997
Genealogical reconstruction of myotonic dystrophy in the Saguenay‐Lac‐Saint‐Jean area (Quebec, Canada)
J Mathieu, M De Braekeleer, C Prévost
Neurology 40 (5), 839-839, 1990
1931990
Autosomal recessive spastic ataxia of Charlevoix–Saguenay
JP Bouchard, A Richter, J Mathieu, D Brunet, TJ Hudson, K Morgan, ...
Neuromuscular disorders 8 (7), 474-479, 1998
1831998
Relationship between chronic hypercapnia and inspiratory-muscle weakness in myotonic dystrophy
P Begin, J Mathieu, J Almirall, A Grassino
American journal of respiratory and critical care medicine 156 (1), 133-139, 1997
1661997
Myotonic dystrophy: clinical assessment of muscular disability in an isolated population with presumed homogeneous mutation
J Mathieu, MD Braekeleer, C Prévost, C Boily
Neurology 42 (1), 203-203, 1992
1611992
Sleep complaints in patients with myotonic dystrophy
L Laberge, P Bégin, J Montplaisir, J Mathieu
Journal of sleep research 13 (1), 95-100, 2004
1552004
Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy
A Duquette, K Roddier, J McNabb‐Baltar, I Gosselin, A St‐Denis, ...
Annals of neurology 57 (3), 408-414, 2005
1412005
Genes, maternal smoking, and the offspring brain and body during adolescence: design of the Saguenay Youth Study
Z Pausova, T Paus, M Abrahamowicz, J Almerigi, N Arbour, M Bernard, ...
Human brain mapping 28 (6), 502-518, 2007
1402007
Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions
ME Arsenault, C Prevost, A Lescault, C Laberge, J Puymirat, J Mathieu
Neurology 66 (8), 1248-1250, 2006
1232006
A polysomnographic study of daytime sleepiness in myotonic dystrophy type 1
L Laberge, P Bégin, Y Dauvilliers, M Beaudry, M Laforte, S Jean, ...
Journal of Neurology, Neurosurgery & Psychiatry 80 (6), 642-646, 2009
1202009
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
1192008
Hereditary motor and sensory neuropathy with agenesis of the corpus callosum
N Dupré, HC Howard, J Mathieu, G Karpati, M Vanasse, JP Bouchard, ...
Annals of neurology 54 (1), 9-18, 2003
1092003
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