index - Connectivité neuromusculaire en santé & pathologies

Dernières publications

Chiffres clés

41 Publications avec texte intégral

Open Access

48 %

Mots clés

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