about
Genes and brain malformations associated with abnormal neuron positioningA developmental and genetic classification for malformations of cortical development: update 2012Bilateral subcortical heterotopia with partial callosal agenesis in a mouse mutantCurrent concepts of polymicrogyria.Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.Polymicrogyria: pathology, fetal origins and mechanisms.GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.GPR56 and the developing cerebral cortex: cells, matrix, and neuronal migrationGenetic malformations of the human frontal lobe.What disorders of cortical development tell us about the cortex: one plus one does not always make twoGermline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposisImpact of GPCRs in clinical medicine: monogenic diseases, genetic variants and drug targetsAsymmetry of Radial and Symmetry of Tangential Neuronal Migration Pathways in Developing Human Fetal Brains.Topological properties of large-scale structural brain networks in children with familial risk for reading difficulties.Distinct genetic influences on cortical surface area and cortical thickness.Quantification and discrimination of abnormal sulcal patterns in polymicrogyriaAbnormal development of the human cerebral cortex.Recent advances in the genetic etiology of brain malformations.The epilepsy phenome/genome project.A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22.Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria.Postsynaptic currents prior to onset of epileptiform activity in rat microgyria.De novo mutations in GRIN1 cause extensive bilateral polymicrogyria.Genetic and environmental influences on cortical surface area and cortical thickness in bipolar disorder.The histopathology of polymicrogyria: a series of 71 brain autopsy studies.Tubacin prevents neuronal migration defects and epileptic activity caused by rat Srpx2 silencing in utero.Verbal and gestural communication in children with bilateral perisylvian polymicrogyria.Review of X-linked syndromes with arthrogryposis or early contractures-aid to diagnosis and pathway identification.Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria.Personality Changes in Bilateral Superior Frontal and Parafalcine Frontoparietal Polymicrogyria: A Rare Case Report.Bilateral perisylvian polymicrogyria with cerebellar dysplasia and ectopic neurohypophysisMalformations of cortical developmentMalformations of cortical development and epilepsy
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Genetics of the polymicrogyria syndromes.
@ast
Genetics of the polymicrogyria syndromes.
@en
type
label
Genetics of the polymicrogyria syndromes.
@ast
Genetics of the polymicrogyria syndromes.
@en
prefLabel
Genetics of the polymicrogyria syndromes.
@ast
Genetics of the polymicrogyria syndromes.
@en
P2860
P356
P1476
Genetics of the polymicrogyria syndromes
@en
P2093
Andermann E
P2860
P304
P356
10.1136/JMG.2004.023952
P407
P577
2005-05-01T00:00:00Z