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Dernières publications
Chiffres clés
45
Publications avec texte intégral
Open Access
49 %
Mots clés
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