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Auteur Mathieu J |
Documents disponibles écrits par cet auteur (74)



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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
Revue : Epigenomics, 12, 23 Titre : DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1 Type de document : Article Auteurs : Breton É ; Legare C ; Overend G ; Guay SP ; Monckton D ; Mathieu J ; Gagnon C ; Richer L ; Gallais B ; Bouchard L Editeur : England Année de publication : 12/2020 Pages : p 2051 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33301350 / DOI : 10.2217/epi-2020-0328
N° Profil MNM : 2020122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33301350 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Disability and rehabilitation Titre : Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1 Type de document : Article Auteurs : Raymond K ; Levasseur M ; Gallais B ; Richer L ; Laberge L ; Petitclerc à ; Mathieu J ; Gagnon C Editeur : England Année de publication : 02/11/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33135946 / DOI : 10.1080/09638288.2020.1837264
N° Profil MNM : 2020111 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33135946 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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A study of impairments in Oculopharyngeal Muscular Dystrophy
Brisson JD, Gagnon C, Brais B, et al.
Muscle & Nerve, 2020
Revue : Muscle & Nerve Titre : A study of impairments in Oculopharyngeal Muscular Dystrophy Type de document : Article Auteurs : Brisson JD, Auteur ; Gagnon C ; Brais B ; Côté I ; Mathieu J Editeur : United States Année de publication : 04/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32270505 / DOI : 10.1002/mus.26888
N° Profil MNM : 2020041 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32270505 Voir aussiAvis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Validity of the Mini-BESTest in adults with myotonic dystrophy type 1
Duchesne E, Hebert LJ, Mathieu J, et al.
Muscle & Nerve, 2020
Revue : Muscle & Nerve Titre : Validity of the Mini-BESTest in adults with myotonic dystrophy type 1 Type de document : Article Auteurs : Duchesne E, Auteur ; Hebert LJ ; Mathieu J ; Côté I ; Roussel MP ; Gagnon C Editeur : United States Année de publication : 04/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32314404 / DOI : 10.1002/mus.26893
N° Profil MNM : 2020042 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32314404 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians
Pellerin D, Aykanat A, Ellezam B, et al.
Annals of neurology, 2020
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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