Dilated cardiomyopathy Congenital muscular dystrophy PABPN1 Myositis Animals Autoimmune diseases COVID-19 Centronuclear myopathy Biomarkers Neuromuscular junction Myasthenia gravis Treatment Exercise FSHD Calcium Myogenesis CRISPRi Myopathy Long read sequencing LMNA AAV RNA biology Skeletal muscle Fibrosis Aging Duchenne muscular dystrophy Nuclear envelope Inflammation Heart Transcriptomics Satellite cell ALS Male Therapy Glutamate Myotonic Dystrophy Mechanotransduction Muscle regeneration Genetics Regeneration Biomarker Dermatomyositis Actin Aged Autoantibodies Satellite cells Congenital myopathy Laminopathie LMNA gene Myoblasts MBNL RNA interference Myotonic Dystrophy type 1 Cytoskeleton Myasthenia Gravis MG Rare diseases Astrocyte Becker muscular dystrophy Neuromuscular disease Outcome measures Neuromuscular diseases Transgenic mouse model Brain Antisense oligonucleotides Fabry disease Thérapie génique Alternative splicing Mouse model Spinal muscular atrophy Cytokines Lamin A/C LMNA gene Myotonic dystrophy type 1 Rare neuromuscular diseases Cell therapy Trinucleotide repeat expansion Amyotrophic lateral sclerosis Myotonic dystrophy Lamin A/C Autoimmunity Cardiomyopathy CTG repeat contractions Humans Motoneuron OPMD Thymus CMS Heart failure Autophagy Genotype phenotype correlation Myopathies DMD Muscle Laminopathies Dynamin 2 Muscular dystrophy Mice Errance diagnostique Laminopathy Gene therapy Dystrophin