index - Connectivité neuromusculaire en santé & pathologies Accéder directement au contenu

Dernières publications

Chiffres clés

41 Publications avec texte intégral

Open Access

48 %

Mots clés

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