A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
about
Epilepsy related to developmental tumors and malformations of cortical developmentDe novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.mTOR signaling in epilepsy: insights from malformations of cortical developmentFetal brain lesions in tuberous sclerosis complex: TORC1 activation and inflammationCellular distribution of vascular endothelial growth factor A (VEGFA) and B (VEGFB) and VEGF receptors 1 and 2 in focal cortical dysplasia type IIB.Temporal lobe sclerosis associated with hippocampal sclerosis in temporal lobe epilepsy: neuropathological features.Hemimegalencephaly with Facial Congenital Infiltrating Lipomatosis in a Child.Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly.Hemimegalencephaly in a patient with coexisting trisomy 21 and hypomelanosis of Ito.Hemimegalencephaly: what happens when children get older?
P2860
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P2860
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
description
2007 nî lūn-bûn
@nan
2007年の論文
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2007年学术文章
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2007年学术文章
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2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
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2007年學術文章
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2007年學術文章
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name
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@en
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@nl
type
label
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@en
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@nl
prefLabel
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@en
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@nl
P2093
P2860
P1476
A neuropathological study of two autopsy cases of syndromic hemimegalencephaly.
@en
P2093
P2860
P304
P356
10.1111/J.1365-2990.2006.00818.X
P577
2007-08-01T00:00:00Z