Epilepsies in twins: genetics of the major epilepsy syndromes.
about
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsyLinkage and association analysis of CACNG3 in childhood absence epilepsyAdvancing epilepsy genetics in the genomic eraGenetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental modelsEpilepsy during pregnancy: focus on management strategiesEpileptic syndromes: From clinic to geneticGlucose transporter 1 deficiency in the idiopathic generalized epilepsiesBurden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsiesCommon genetic variation and susceptibility to partial epilepsies: a genome-wide association studyGenome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.Sequencing of the GRIK1 gene in patients with juvenile absence epilepsy does not reveal mutations affecting receptor structure.Seizure susceptibility is associated with altered protein expression of voltage-gated calcium channel subunits in inferior colliculus neurons of the genetically epilepsy-prone ratAbsence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4Australian Twin Registry: 30 years of progress.Rare and common epilepsies converge on a shared gene regulatory network providing opportunities for novel antiepileptic drug discovery.Clinical predictors of 2-year outcome of resective epilepsy surgery in adults with refractory epilepsy: a cohort studyIdiopathic epilepsies with a complex mode of inheritance.The genetics of status epilepticus.Recent advances in the genetics of epilepsy: insights from human and animal studies.Epilepsy genetics--past, present, and futureGenetic testing in the epilepsies-developments and dilemmas.Familial clustering of seizure types within the idiopathic generalized epilepsies.Epilepsy genes: the link between molecular dysfunction and pathophysiology.Genetics of epilepsyGenetics of epilepsy: The testimony of twins in the molecular eraAn Etiological Model for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studiesGenetically complex epilepsies, copy number variants and syndrome constellations.Genes and mutations in idiopathic epilepsy.Progress in the genetics of the partial epilepsies.Channelopathies can cause epilepsy in man.A genetic interaction network model of a complex neurological disease.Heritability of subcortical volumetric traits in mesial temporal lobe epilepsy.Does epilepsy run in families? Getting closer to the answerEvidence for distinct genetic influences on generalized and localization-related epilepsy.Cellular and network mechanisms of genetically-determined absence seizures.Importance of genetic factors in the occurrence of epilepsy syndrome type: a twin study.Epi4K: gene discovery in 4,000 genomes.Advances in epilepsy genetics and genomics.
P2860
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P2860
Epilepsies in twins: genetics of the major epilepsy syndromes.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
@zh-sg
1998年學術文章
@yue
1998年學術文章
@zh-hant
name
Epilepsies in twins: genetics of the major epilepsy syndromes.
@en
Epilepsies in twins: genetics of the major epilepsy syndromes.
@nl
type
label
Epilepsies in twins: genetics of the major epilepsy syndromes.
@en
Epilepsies in twins: genetics of the major epilepsy syndromes.
@nl
prefLabel
Epilepsies in twins: genetics of the major epilepsy syndromes.
@en
Epilepsies in twins: genetics of the major epilepsy syndromes.
@nl
P2860
P356
P1433
P1476
Epilepsies in twins: genetics of the major epilepsy syndromes.
@en
P2093
P2860
P304
P356
10.1002/ANA.410430405
P577
1998-04-01T00:00:00Z