index - Connectivité neuromusculaire en santé & pathologies

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MBNL Deficiency Conduction disease ALS HDAC motor neuron neuromuscular junction reinnervation Jonction neuro musculaire Calcium channel 80 and over Dimerization Acetyltransferase Amyloid Gene Expression Regulation Cluster Analysis Cell Cycle Proteins/chemistry/genetics/metabolism Synaptotagmin2 MuSK Amyotrophic lateral sclerosis Distal myopathy Amyotrophic Lateral Sclerosis/genetics Disability Body Patterning Animals Neuromuscular disease Multiple sclerosis Treatment delay CMS Expression Acetylcholinesterase Hereditary/genetics Hypokalaemic periodic paralysis Clinical trial Wnt MRC ¼ Medical Research Council Receptors Chemokines Drainage HSP70 Heat-Shock Proteins/genetics/metabolism Cytokines Agrin Actin cytoskeleton Genetic Association Studies Clinical trials Epidemiology Mexiletine Chloride channel Aging CLS Nondystrophic myotonias NMJ Precision medicine Cognitive decline Minigene Female Neuromuscular junction Diseases Developmental Humans Motoneuron Brain Rare diseases Database Embryo Experimental disease models LRP4 Congenital myasthenic syndromes Jonction neuromusculaire Heart failure Acetylcholine receptor clustering M3243AG Ca V Alzheimer's disease Biological Markers Cercopithecus aethiops Congenital myopathy COVID-19 Myotonic Dystrophy Congenital myasthenic syndrome Non-dystrophic myotonia Knockout mouse Autoimmune IL22RA2 IL-22 binding protein isoform GFPT1 COS Cells HEK293 Cells Lithium chloride Gating pore current Abbreviations CMAP ¼ compound muscle action potential Frontotemporal lobar degeneration Actionable genes Cholinergic Paramyotonia congenita Adult SMA Jonction Neuromusculaire NMJ Aged HypoPP ¼ hypokalaemic periodic paralysis Frontotemporal Dementia/genetics Longitudinal progression Myotonia congenita Awareness Mutation Butyrylcholinesterase