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Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucomaGenetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsIon channels in genetic and acquired forms of epilepsy.Common variants of KCNJ10 are associated with susceptibility and anti-epileptic drug resistance in Chinese genetic generalized epilepsiesGenetic basis of pediatric epilepsy syndromes.A visual migraine aura locus maps to 9q21-q22GABAergic neuron deficit as an idiopathic generalized epilepsy mechanism: the role of BRD2 haploinsufficiency in juvenile myoclonic epilepsy.Impaired action potential initiation in GABAergic interneurons causes hyperexcitable networks in an epileptic mouse model carrying a human Na(V)1.1 mutationMolecular basis of decreased Kir4.1 function in SeSAME/EAST syndrome.A genetic interaction network model of a complex neurological disease.Candidate genes for idiopathic epilepsy in four dog breeds.Gene-wide tagging study of the association between KCNT1 polymorphisms and the susceptibility and efficacy of genetic generalized epilepsy in Chinese population.Contrast gain control abnormalities in idiopathic generalized epilepsy.Comparative proteomic approach in rat model of absence epilepsy.No relation between EFHC2 gene polymorphism and Idiopathic generalized epilepsyShared loci for migraine and epilepsy on chromosomes 14q12-q23 and 12q24.2-q24.3.Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14.Functional analysis of a de novo GRIN2A missense mutation associated with early-onset epileptic encephalopathy.The methylation hypothesis: do epigenetic chromatin modifications play a role in epileptogenesis?HCN and KV7 (M-) channels as targets for epilepsy treatment.Genetic biomarkers in epilepsy.The role of genetic testing in epilepsy diagnosis and management.[Genetics of idiopathic epilepsies].PRRT2 mutations are the major cause of benign familial infantile seizures.A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p.Common variants of APOE are associated with anti-epileptic drugs resistance in Han Chinese patients.Pharmakogenetik
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Genetic mechanisms in idiopathic epilepsies.
@en
Genetic mechanisms in idiopathic epilepsies.
@nl
type
label
Genetic mechanisms in idiopathic epilepsies.
@en
Genetic mechanisms in idiopathic epilepsies.
@nl
prefLabel
Genetic mechanisms in idiopathic epilepsies.
@en
Genetic mechanisms in idiopathic epilepsies.
@nl
P1476
Genetic mechanisms in idiopathic epilepsies.
@en
P2093
Holger Lerche
Yvonne G Weber
P2860
P304
P356
10.1111/J.1469-8749.2008.03058.X
P577
2008-09-01T00:00:00Z