Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options.
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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsMicrocephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitorsCerebral cortex expansion and folding: what have we learned?Partial epilepsy: A pictorial review of 3 TESLA magnetic resonance imaging featuresPhysical biology of human brain developmentDISC1: a key lead in studying cortical development and associated brain disordersGenetic Basis of Brain MalformationsA Case for Microtubule Vulnerability in Amyotrophic Lateral Sclerosis: Altered Dynamics During DiseasePeriventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 geneAn inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation.Bilateral subcortical heterotopia with partial callosal agenesis in a mouse mutantNovel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction.Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis.Dampened hippocampal oscillations and enhanced spindle activity in an asymptomatic model of developmental cortical malformationsLayer-specific gene expression in epileptogenic type II focal cortical dysplasia: normal-looking neurons reveal the presence of a hidden laminar organization.Renewed focus on the developing human neocortex.Gene expression analysis of tuberous sclerosis complex cortical tubers reveals increased expression of adhesion and inflammatory factors.Polymicrogyria: pathology, fetal origins and mechanisms.Malformations of cortical development with good clinical outcome: a case report and review of literature.Increased temporolimbic cortical folding complexity in temporal lobe epilepsy.Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations.Analysis of epigenetic factors in mouse embryonic neural stem cells exposed to hyperglycemiaControl of cortical neuronal migration by glutamate and GABAPolymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization.Fish do not feel pain and its implications for understanding phenomenal consciousness.Malformations of cortical development: clinical features and genetic causesNodule excitability in an animal model of periventricular nodular heterotopia: c-fos activation in organotypic hippocampal slices.Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disabilityIn vitro effects of fetal rat cerebrospinal fluid on viability and neuronal differentiation of PC12 cells.Are Somatic Mutations in Cortical Development the One Bad Apple That Spoils the Bunch?Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations.POU-III transcription factors (Brn1, Brn2, and Oct6) influence neurogenesis, molecular identity, and migratory destination of upper-layer cells of the cerebral cortexMutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephalyAlterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletions.Mutation of the variant alpha-tubulin TUBA8 results in polymicrogyria with optic nerve hypoplasia.Neuropathology of brain and spinal malformations in a case of monosomy 1p36.miRNAs: Key Players in Neurodegenerative Disorders and EpilepsySurgical management of medically refractory epilepsy in patients with polymicrogyria.Basic mechanisms of MCD in animal modelsRole of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.
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P2860
Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on 08 February 2008
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vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Abnormal development of the hu ...... quences and treatment options.
@en
Abnormal development of the hu ...... quences and treatment options.
@nl
type
label
Abnormal development of the hu ...... quences and treatment options.
@en
Abnormal development of the hu ...... quences and treatment options.
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prefLabel
Abnormal development of the hu ...... quences and treatment options.
@en
Abnormal development of the hu ...... quences and treatment options.
@nl
P1476
Abnormal development of the hu ...... quences and treatment options.
@en
P2093
A James Barkovich
Renzo Guerrini
P304
P356
10.1016/J.TINS.2007.12.004
P577
2008-02-08T00:00:00Z