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

Dernières publications

Chiffres clés

41 Publications with fulltext

Open Access

48 %

Mots clés

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