Related references
Note: Only part of the references are listed.Metabolic complications in myotonic dystrophy type 1: A cross-sectional survey using the National Registry of Japan
Manami Hama et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2021)
The Canadian Neuromuscular Disease Registry 2010-2019: A Decade of Facilitating Clinical Research Through a Nationwide, Pan-Neuromuscular Disease Registry
V Hodgkinson et al.
JOURNAL OF NEUROMUSCULAR DISEASES (2021)
Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes
Gayle Overend et al.
HUMAN MOLECULAR GENETICS (2019)
The myotonic dystrophy experience: a North American cross-sectional study
Katharine A. Hagerman et al.
MUSCLE & NERVE (2019)
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study
Salvatore Rossi et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2019)
Molecular genetics of congenital myotonic dystrophy
Stella Lanni et al.
NEUROBIOLOGY OF DISEASE (2019)
A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management
Emmanuelle Lagrue et al.
NEUROLOGY (2019)
Respiratory dysfunction in myotonic dystrophy type 1: A systematic review
A. M. Hawkins et al.
NEUROMUSCULAR DISORDERS (2019)
Cognitive impairment and quality of life in patients with myotonic dystrophy type 1
Haruo Fujino et al.
MUSCLE & NERVE (2018)
A 9-year follow-up study of quantitative muscle strength changes in myotonic dystrophy type 1
Cynthia Gagnon et al.
JOURNAL OF NEUROLOGY (2018)
Distribution and Structure of DM2 Repeat Tract Alleles in the German Population
Alexis S. Mahyera et al.
FRONTIERS IN NEUROLOGY (2018)
Eight years after an international workshop on myotonic dystrophy patient registries: case study of a global collaboration for a rare disease
Libby Wood et al.
ORPHANET JOURNAL OF RARE DISEASES (2018)
Myotonic Dystrophies: Targeting Therapies for Multisystem Disease
Samantha LoRusso et al.
NEUROTHERAPEUTICS (2018)
The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research
Libby Wood et al.
JOURNAL OF NEUROLOGY (2017)
A REVIEW OF MUSCLE-AND PERFORMANCE-BASED ASSESSMENT INSTRUMENTS IN DM1
Tara Symonds et al.
MUSCLE & NERVE (2017)
Relationships between grip strength, myotonia, and CTG expansion in myotonic dystrophy type 1
Jean-Yves Hogrel et al.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2017)
Population-based values and abnormalities of the electrocardiogram in the general Dutch population: The LifeLines Cohort Study
M. Yldau van der Ende et al.
CLINICAL CARDIOLOGY (2017)
The cognitive profile of myotonic dystrophy type 1: A systematic review and meta-analysis
Kees Okkersen et al.
CORTEX (2017)
Myotonic dystrophy: disease repeat range, penetrance, age of onset, and relationship between repeat size and phenotypes
Kevin Yum et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2017)
A Systematic Review and Meta-analysis on the Epidemiology of the Muscular Dystrophies
Jean K. Mah et al.
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES (2016)
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophy
Nicholas E. Johnson et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2016)
Association of Age, Sex, Body Size and Ethnicity with Electrocardiographic Values in Community-based Older Asian Adults
Eugene S. J. Tan et al.
HEART LUNG AND CIRCULATION (2016)
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry
Teresinha Evangelista et al.
JOURNAL OF NEUROLOGY (2016)
Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study
Celine Dogan et al.
PLOS ONE (2016)
Natural history of skeletal muscle involvement in myotonic dystrophy type 1: a retrospective study in 204 cases
Jean-Pierre Bouchard et al.
JOURNAL OF NEUROLOGY (2015)
Myotonic dystrophy: diagnosis, management and new therapies
Chris Turner et al.
CURRENT OPINION IN NEUROLOGY (2014)
Epiretinal membrane: a treatable cause of visual disability in myotonic dystrophy type 1
Hannah M. Kersten et al.
JOURNAL OF NEUROLOGY (2014)
Prevalence of Muscular Dystrophies: A Systematic Literature Review
Alice Theadom et al.
NEUROEPIDEMIOLOGY (2014)
Nationwide patient registry for GNE myopathy in Japan
Madoka Mori-Yoshimura et al.
ORPHANET JOURNAL OF RARE DISEASES (2014)
Fatigue and daytime sleepiness scale in myotonic dystrophy type 1
Mieke C. E. Hermans et al.
MUSCLE & NERVE (2013)
Characteristics of Japanese Duchenne and Becker muscular dystrophy patients in a novel Japanese national registry of muscular dystrophy (Remudy)
Harumasa Nakamura et al.
ORPHANET JOURNAL OF RARE DISEASES (2013)
Ocular motor function in relation to gross motor function in congenital and childhood myotonic dystrophy type 1
Eva Aring et al.
ACTA OPHTHALMOLOGICA (2012)
Psychiatric and cognitive phenotype of childhood myotonic dystrophy type 1
Marie Douniol et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2012)
Myotonic dystrophy type 2 is rare in the Japanese population
Tohru Matsuura et al.
JOURNAL OF HUMAN GENETICS (2012)
The myotonic dystrophies: molecular, clinical, and therapeutic challenges
Bjarne Udd et al.
LANCET NEUROLOGY (2012)
Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1)
Chad Heatwole et al.
NEUROLOGY (2012)
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland
Tiina Suominen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Patient Registries and Trial Readiness in Myotonic Dystrophy – TREAT-NMD/Marigold International Workshop Report
Rachel Thompson et al.
NEUROMUSCULAR DISORDERS (2009)
Fatigue and daytime sleepiness in patients with myotonic dystrophy type 1: To lump or split?
Luc Laberge et al.
NEUROMUSCULAR DISORDERS (2009)
Health-related quality of life in myotonic dystrophy type 1 and its relationship with cognitive and emotional functioning
G Antonini et al.
JOURNAL OF REHABILITATION MEDICINE (2006)
Severity of cardiac conduction involvement and arrhythmias in myotonic dystrophy type 1 correlates with age and CTG repeat length
WJ Groh et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2002)