Gender as a Modifying Factor Influencing Myotonic Dystrophy Type 1 Phenotype Severity and Mortality: A Nationwide Multiple Databases Cross-Sectional Observational Study - Dogan, Celine; De Antonio, Marie; Hamroun, Dalil; Varet, Hugo; Fabbro, Marianne; Rougier, Felix; Amarof, Khadija; Arne Bes, Marie-Christine; Bedat-Millet, Anne-Laure; Behin, Anthony; Bellance, Remi; Bouhour, Françoise; et al. (PloS one, 2016)
Keywords: Abnormalities; Adult; Biology and Life Sciences; Care and treatment; Cataracts; Chronology; Clinical trials; Cognitive ability; Complications and side effects; Cross-Sectional Studies; Databases, Factual; Development and progression; Digestive tract; Dysphagia; Dystrophy; Economic conditions; Economics; Female; Females; Gastrointestinal tract; Gender differences; Gene expression; Genetics; Genotype & phenotype; Health services; Heart diseases; Human genetics; Humans; Impact analysis; Kinases; Life Sciences; Male; Males; Medical research; Medicine and Health Sciences; Morbidity; Mortality; Muscular dystrophy; Myotonia; Myotonic dystrophy; Myotonic Dystrophy - epidemiology; Myotonic Dystrophy - mortality; Neurology; Obesity; Observational studies; Patient outcomes; People and Places; Phenotype; Protein kinases; Santé publique et épidémiologie; Sex Distribution; Socioeconomic Factors; Studies; Thyroid; Trinucleotide repeat diseases; United States; France; Cataracts; Obesity; Death rates; Myotonic dystrophy; Maternal inheritance; Dysphagia; Morbidity; Cognitive impairment