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DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1
Breton É, Legare C, Overend G, et al.
Epigenomics, 2020, 12, 23, p 2051
Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1
Raymond K, Levasseur M, Gallais B, et al.
Disability and rehabilitation, 2020
A study of impairments in Oculopharyngeal Muscular Dystrophy
Brisson JD, Gagnon C, Brais B, et al.
Muscle & Nerve, 2020
Validity of the Mini-BESTest in adults with myotonic dystrophy type 1
Duchesne E, Hebert LJ, Mathieu J, et al.
Muscle & Nerve, 2020
Clinical, morphological and genetic characterization of Brody disease: an international study of 40 patients
Molenaar JP, Verhoeven JI, Rodenburg RJ, et al.
Brain : a journal of neurology, 2020, 143, 2, p 452
Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians
Pellerin D, Aykanat A, Ellezam B, et al.
Annals of neurology, 2020
Predicting daytime sleepiness and fatigue: a 9-year prospective study in myotonic dystrophy type 1
Laberge L, Gallais B, Auclair J, et al.
Journal of neurology, 2019
Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes.
Overend G, Legare C, Mathieu J, et al.
Human molecular genetics, 2019, 28, n13, p 2245
The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care.
De Antonio M, Dogan C, Daidj F, et al.
Orphanet journal of rare diseases, 2019, 14, n1, p 122
DMPK gene DNA methylation levels are associated with muscular and respiratory profiles in DM1
Legare C, Overend G, Guay SP, et al.
Neurology. Genetics, 2019, 5, 3
Progressive Decline in Daily and Social Activities: A 9-year Longitudinal Study of Participation in Myotonic Dystrophy Type 1
Raymond K, Levasseur M, Mathieu J, et al.
Archives of physical medicine and rehabilitation, 2019
A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1
Gagnon C, Petitclerc É, Kierkegaard M, et al.
Journal of neurology, 2018
Relationships between Lower Limb Muscle Strength Impairments and Physical Limitations in DM1
Petitclerc É, Hebert LJ, Mathieu J, et al.
Journal of Neuromuscular Diseases, 2018, 5, 2, p 215
CpG Methylation, a Parent-of-Origin Effect for Maternal-Biased Transmission of Congenital Myotonic Dystrophy
Barbé L, Lanni S, Lopez-Castel A, et al.
American journal of human genetics, 2017, 100, 3, p 488
Participation restriction in childhood phenotype of myotonic dystrophy type 1: a systematic retrospective chart review
Gagnon C, Kierkegaard M, Blackburn C, et al.
Developmental medicine and child neurology, 2017, 59, 3, p 291
Lower limb muscle strength impairment in late-onset and adult myotonic dystrophy type 1 phenotypes
Petitclerc É, Hebert LJ, Mathieu J, et al.
Muscle & Nerve, 2017, 56, 1, p 57
Cognitive decline over time in adults with myotonic dystrophy type 1: A 9-year longitudinal study
Gallais B, Gagnon C, Mathieu J, et al.
Neuromuscular disorders : NMD, 2017, 27, 1, p 61
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
Raymond K, Levasseur M, Mathieu J, et al.
Neuromuscular disorders : NMD, 2017, 27, 7, p 673
Stanford Chronic Disease Self-Management Program in myotonic dystrophy: New opportunities for occupational therapists : Stanford Chronic Disease Self-Management Program dans la dystrophie myotonique : De nouvelles opportunités pour les ergothérapeutes
Raymond K, Levasseur M, Chouinard MC, et al.
Canadian journal of occupational therapy. Revue canadienne d'ergotherapie, 2016, 83, 3, p 166
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencing
Levesque S, Auray-Blais C, Gravel E, et al.
Orphanet journal of rare diseases, 2016, 11
Psychological characteristics of patients with myotonic dystrophy type 1
Bertrand JA, Jean S, Laberge L, et al.
Acta neurologica Scandinavica, 2015, 132, 1, p 49
Anticipation in myotonic dystrophy type 1 parents with small CTG expansions
Pratte A, Prévost C, Puymirat J, et al.
American Journal of Medical Genetics Part A, 2015, 167A, 4, p 708
DM1 Patients with Small CTG Expansions are also at Risk of Severe Conduction Abnormalities
Denicourt M, Pham MT, Mathieu J, et al.
Journal of Neuromuscular Diseases, 2015, 2, 1, p. 99-105
Assessing upper extremity capacity as a potential indicator of needs related to household activities for rehabilitation services in people with myotonic dystrophy type 1
Raymond K, Auger LP, Cormier MF, et al.
Neuromuscular disorders : NMD, 2015, 25, 6, p 522
Cognitive deficits associated with sleep apnea in myotonic dystrophy type 1
Gallais B, Gagnon C, Mathieu J, et al.
Journal of Neuromuscular Diseases, 2014, 1, p. 95-98
