Neurographie IRM quantitative de patients atteints d’une neuropathie de Charcot-Marie-Tooth de type 1A
Hypersensitivity infusion-associated reactions induced by Enzyme replacement Therapy (Myozyme) in Pompe disease and efficacy of SWORD : a simplified desensitization protocol
Investigating the role of mechanical tension during sarcomere self-organisation in human iPSC-derived myofibers
Essential role of the ESCRT-O hepatocyte growth factor regulated tyrosine kinase substrate HRS/HGS protein in muscle cell biology
Role of caveolae in muscle function and pathophysiology of caveolinopathies
Inhibition of p38 MAPK pathway combined with new biomimetic scaffolds promotes ex vivo expansion of undifferentiated adult muscle stem cells
Dermatomyosite à anticorps anti-TIF1g de l’adulte : la présence d’anti-TIF1gamma-igG2 est associée à la mortalité
TGFb signaling curbs cell fusion and muscle regeneration
Novel mutations in PYROXD1-related myopathy
Rôle inattendu du tissu adipeux dans le processus de régénération musculaire
Rev-erb-alpha exacerbates endoplasmic reticulum stress-induced apoptosis in mouse skeletal muscle
Single-cell functional analysis of aged and dystrophic muscle identifies a novel myogenic population distinct from satellite cells
Relations Génotype-Phénotype des mutations du gène de la filamine C
Étude du rôle de Vangl2, protéine centrale de la voie de signalisation Wnt polarité planaire, dans la connectivité neuromusculaire
Diagnostic des myopathies en Afrique de l'Ouest : expérience de quatre pays
Does abnormal skeletal muscle plasticity contribute to Lamin-related Congenital Muscular Dystrophy (L-CMD)?
Investigation of calcium current properties and leak conductance in mouse muscle fibers expressing the type 1 Hypokalemic Periodic Paralysis V876E mutant calcium channel
Refining myotonic dystrophy type 1 clinical classification : contribution of DM-Scope nationwide registry
Impact of an antioxidant treatment on recombinant adeno-associated vector-mediated gene transfer in a mouse model of Duchenne muscular dystrophy
Dynamics of Triad
Mechanotransduction underlying tendon cell differentiation
Gasp-1 overexpression leads to a deregulation of adiposity and glucose homeostasis in adult mice
Mutations in the SOCE genes STIM1, ORAI1 and CASQ1 cause tubular aggregate myopathy (TAM)
FATopathie: nouvelle pathologie neuromusculaire causée par des mutations de FAT1
Alterations of the microvascular system in chronic myopathies and functional repercussions on the muscle tissue