index - Connectivité neuromusculaire en santé & pathologies

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