about
De novo mutations in epileptic encephalopathiesNINDS epilepsy and autism spectrum disorders workshop reportEpileptic syndromes: From clinic to geneticIntegrative biological analysis for neuropsychopharmacologyMapping genetic modifiers of survival in a mouse model of Dravet syndrome.WONOEP appraisal: new genetic approaches to study epilepsyThe hidden genetics of epilepsy-a clinically important new paradigm.Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrumOligogenic heterozygosity in individuals with high-functioning autism spectrum disorders.Genetic [corrected] insights into the causes and classification of [corrected] cerebral palsies.Advances in epilepsy genetics and genomics.Array comparative genomic hybridization: results from an adult population with drug-resistant epilepsy and co-morbiditiesGenetic variations and associated pathophysiology in the management of epilepsy.Temperature-dependent changes in neuronal dynamics in a patient with an SCN1A mutation and hyperthermia induced seizuresGenome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.Dissecting the genetic basis of myoclonic-astatic epilepsy.Developmental psychopathology: the role of structural variation in the genome.Advances in genetic diagnosis of neurological disorders.Refractory epilepsy in children.The Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Epilepsy in Paediatric Patients.A subset of genomic alterations detected in rolandic epilepsies contains candidate or known epilepsy genes including GRIN2A and PRRT2.From genetics to genomics of epilepsy.How should children with West syndrome be efficiently and accurately investigated? Results from the National Infantile Spasms Consortium.Epileptic encephalopathies of the Landau-Kleffner and continuous spike and waves during slow-wave sleep types: genomic dissection makes the link with autism.Targeted capture and sequencing for detection of mutations causing early onset epileptic encephalopathy.Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.GPR37L1 modulates seizure susceptibility: Evidence from mouse studies and analyses of a human GPR37L1 variant.Epilepsy with cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH.Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.A survey of seizures and current treatments in 15q duplication syndrome.The genetic landscape of infantile spasmsRare gene deletions in genetic generalized and Rolandic epilepsies
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Epilepsy and the new cytogenetics.
@ast
Epilepsy and the new cytogenetics.
@en
Epilepsy and the new cytogenetics.
@nl
type
label
Epilepsy and the new cytogenetics.
@ast
Epilepsy and the new cytogenetics.
@en
Epilepsy and the new cytogenetics.
@nl
prefLabel
Epilepsy and the new cytogenetics.
@ast
Epilepsy and the new cytogenetics.
@en
Epilepsy and the new cytogenetics.
@nl
P2860
P1433
P1476
Epilepsy and the new cytogenetics.
@en
P2093
Heather C Mefford
John C Mulley
P2860
P304
P356
10.1111/J.1528-1167.2010.02932.X
P577
2011-01-26T00:00:00Z