Loading...
Dernières publications
Chiffres clés
Open Access
49 %
Mots clés
Jonction neuro musculaire
Jonction Neuromusculaire NMJ
Female
Actionable genes
Rare diseases
Agrin
Embryo
Biological Markers
CLS
Conduction disease
IL-22 binding protein isoform
Brain
Congenital myopathy
Deficiency
IL22RA2
Cluster Analysis
Amyloid
Congenital myasthenic syndrome
Paramyotonia congenita
Expression
COVID-19
Amyotrophic lateral sclerosis
Chemokines
ALS HDAC motor neuron neuromuscular junction reinnervation
MBNL
Multiple sclerosis
Congenital myasthenic syndromes
Neuromuscular disease
GFPT1
Non-dystrophic myotonia
Clinical trials
Lithium chloride
MuSK
Awareness
Frontotemporal lobar degeneration
Gating pore current Abbreviations CMAP ¼ compound muscle action potential
Epidemiology
Cercopithecus aethiops
Disability
HEK293 Cells
HypoPP ¼ hypokalaemic periodic paralysis
Chloride channel
Jonction neuromusculaire
Drainage
Cell Cycle Proteins/chemistry/genetics/metabolism
80 and over
CMS
NMJ
LRP4
Cytokines
Hypokalaemic periodic paralysis
COS Cells
Synaptotagmin2
Longitudinal progression
Adult SMA
Motoneuron
Treatment delay
Butyrylcholinesterase
Precision medicine
Minigene
Wnt
Knockout mouse
Heart failure
Mexiletine
Aged
Cell-cell communication
Calcium channel
Frontotemporal Dementia/genetics
Ca V
Cholinergic
Clinical trial
Myotonia congenita
Developmental
Experimental disease models
Database
Mutation
Actin cytoskeleton
Animals
Myotonic Dystrophy
Humans
HSP70 Heat-Shock Proteins/genetics/metabolism
Neuromuscular junction
Body Patterning
Dimerization
Autoimmune
Nondystrophic myotonias
Aging
Distal myopathy
Diseases
Alzheimer's disease
Amyotrophic Lateral Sclerosis/genetics
Genetic Association Studies
Cognitive decline
Acetylcholinesterase
Acetylcholine receptor clustering
M3243AG
Gene Expression Regulation
Hereditary/genetics
Receptors
Acetyltransferase