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Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2The α2B-adrenergic receptor is mutant in cortical myoclonus and epilepsyDe novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndromeLinkage and association analysis of CACNG3 in childhood absence epilepsyIncreased sensitivity of the neuronal nicotinic receptor alpha 2 subunit causes familial epilepsy with nocturnal wandering and ictal fearDefinition and diagnostic criteria of sleep-related hypermotor epilepsyAntiepileptic Drug Treatment in Children with EpilepsyGenetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsThe medical and surgical treatment of tumoral seizures: current and future perspectivesMutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortexSubcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with femalesEpileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testingGenetic malformations of cortical developmentGenetic malformations of the cerebral cortex and epilepsyBenign familial neonatal-infantile seizures: characterization of a new sodium channelopathyXp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathyAbnormal phonologic processing in familial lateral temporal lobe epilepsy due to a new LGI1 mutation
P50
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P50
subject
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Renzo Guerrini
@ast
Renzo Guerrini
@en
Renzo Guerrini
@es
Renzo Guerrini
@nl
Renzo Guerrini
@sl
type
label
Renzo Guerrini
@ast
Renzo Guerrini
@en
Renzo Guerrini
@es
Renzo Guerrini
@nl
Renzo Guerrini
@sl
prefLabel
Renzo Guerrini
@ast
Renzo Guerrini
@en
Renzo Guerrini
@es
Renzo Guerrini
@nl
Renzo Guerrini
@sl