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