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Cognitive decline over time in adults with myotonic dystrophy type 1: a 9-year longitudinal study

Neuromuscular disorders : NMD, 2017-01, Vol.27 (1), p.61-72

2017

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Rest-activity disturbances and light exposure in myotonic dystrophy type 1 patients with apathy: An exploratory study using actigraphy

Journal of affective disorders reports, 2023-12, Vol.14, p.100637, Article 100637

2023

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Accomplishment of instrumental activities of daily living and its relationship with cognitive functions in adults with myotonic dystrophy type 1 childhood phenotype: an exploratory study

BMC Psychology, 2021-04, Vol.9 (1), p.56-56, Article 56

2021

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Understanding factors hampering activities of daily living performance in childhood‐onset myotonic dystrophy phenotypes

Developmental medicine and child neurology, 2020-06, Vol.62 (6), p.665-665

2020

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Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease

Quality of life research, 2015-11, Vol.24 (11), p.2615-2623

2015

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Instrumental activities of daily living in adults with the DM1 childhood phenotype: going beyond motor impairments

Neuromuscular disorders : NMD, 2022-04, Vol.32 (4), p.313-320

2022

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Myotonic dystrophy type 1: reasons to be OPTIMISTIC

Lancet neurology, 2018-08, Vol.17 (8), p.652-653

2018

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A supervised resistance training program in women with myotonic dystrophy type 1

Journal of the neurological sciences, 2023-12, Vol.455, p.122026, Article 122026

2023

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Predicting daytime sleepiness and fatigue: a 9-year prospective study in myotonic dystrophy type 1

Journal of neurology, 2020-02, Vol.267 (2), p.461-468

2020

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Do classical and computerized cognitive tests have equal intrarater reliability in myotonic dystrophy type 1?

Neuromuscular disorders : NMD, 2023-06, Vol.33 (6), p.490-497

2023

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Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1

Disability and rehabilitation, 2022-06, Vol.44 (12), p.2615-2631

2022

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Further evidence for the reliability and validity of the Fatigue and Daytime Sleepiness Scale

Journal of the neurological sciences, 2017-04, Vol.375, p.23-26

2017

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Prevalence and correlates of apathy in myotonic dystrophy type 1

BMC neurology, 2015-08, Vol.15 (1), p.148-148, Article 148

2015

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Responsiveness of Daytime Sleepiness and Fatigue Scales in Myotonic Dystrophy Type 1

Canadian journal of neurological sciences, 2022-03, Vol.49 (2), p.287-290

2022

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Resistance training in women with myotonic dystrophy type 1: a multisystemic therapeutic avenue

Neuromuscular disorders : NMD, 2024-07, Vol.40, p.38-51

2024

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Évaluation du rythme veille-sommeil chez des adultes avec la forme infantile de la dystrophie myotonique de type 1 : une étude en actimétrie

Médecine du sommeil, 2024-03, Vol.21 (1), p.64-65

2024

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207th ENMC Workshop on chronic respiratory insufficiency in myotonic dystrophies: Management and implications for research, 27–29 June 2014, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2015-05, Vol.25 (5), p.432-442

2015

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Further evidence for the reliability and validity of the f atigue and d aytime s leepiness s cale

Journal of the neurological sciences, 2016

2016

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DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1

Epigenomics, 2020-12, Vol.12 (23), p.2051-2064

2020

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A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

Journal of neuromuscular diseases, 2018, Vol.5 (3), p.279-294

2018

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Becoming a research participant: Decision-making needs of individuals with neuromuscular diseases

Translational science of rare diseases, 2023-07, Vol.6 (3), p.39-57

2023

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Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review

Journal of neuromuscular diseases, 2024-01, Vol.11 (3), p.567-577

2024

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A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

Journal of neuromuscular diseases, 2018-08, Vol.5 (3), p.279-294

2018

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A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

Journal of neuromuscular diseases, 2018-08, Vol.5 (3), p.279-294

2018

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Cognitive decline over time in adults with myotonic dystrophy type 1: a 9-year longitudinal study

Rest-activity disturbances and light exposure in myotonic dystrophy type 1 patients with apathy: An exploratory study using actigraphy

Accomplishment of instrumental activities of daily living and its relationship with cognitive functions in adults with myotonic dystrophy type 1 childhood phenotype: an exploratory study

Understanding factors hampering activities of daily living performance in childhood‐onset myotonic dystrophy phenotypes

Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease

Instrumental activities of daily living in adults with the DM1 childhood phenotype: going beyond motor impairments

Myotonic dystrophy type 1: reasons to be OPTIMISTIC

A supervised resistance training program in women with myotonic dystrophy type 1

Predicting daytime sleepiness and fatigue: a 9-year prospective study in myotonic dystrophy type 1

Do classical and computerized cognitive tests have equal intrarater reliability in myotonic dystrophy type 1?

Predictors of participation restriction over a 9-year period in adults with myotonic dystrophy type 1

Further evidence for the reliability and validity of the Fatigue and Daytime Sleepiness Scale

Prevalence and correlates of apathy in myotonic dystrophy type 1

Responsiveness of Daytime Sleepiness and Fatigue Scales in Myotonic Dystrophy Type 1

Resistance training in women with myotonic dystrophy type 1: a multisystemic therapeutic avenue

Évaluation du rythme veille-sommeil chez des adultes avec la forme infantile de la dystrophie myotonique de type 1 : une étude en actimétrie

207th ENMC Workshop on chronic respiratory insufficiency in myotonic dystrophies: Management and implications for research, 27–29 June 2014, Naarden, The Netherlands

267th ENMC International workshop: psychological interventions for improving quality of life in slowly progressive neuromuscular disorders

Further evidence for the reliability and validity of the f atigue and d aytime s leepiness s cale

DNA methylation at the DMPK gene locus is associated with cognitive functions in myotonic dystrophy type 1

A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

Becoming a research participant: Decision-making needs of individuals with neuromuscular diseases

Patient-Reported Outcome Measures in Neuromuscular Diseases: A Scoping Review

A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

A Review of Psychopathology Features, Personality, and Coping in Myotonic Dystrophy Type 1

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