The histopathology of polymicrogyria: a series of 71 brain autopsy studies (Q50577595)

15 March 2018

title

The histopathology of polymicrogyria: a series of 71 brain autopsy studies (English)

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Anna C Jansen

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author name string

Yves Robitaille

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Mrinalini Honavar

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Nandini Mullatti

4

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Richard J Leventer

5

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Eva Andermann

6

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Frederick Andermann

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Waney Squier

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publication date

14 July 2015

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Developmental Medicine and Child Neurology

published in

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volume

58

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issue

1

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page(s)

39-48

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Genetics of the polymicrogyria syndromes.

cites work

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Clinical and imaging heterogeneity of polymicrogyria: a study of 328 patients

21 January 2018

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Polymicrogyria: a common and heterogeneous malformation of cortical development

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MRI analysis of sulcation morphology in polymicrogyria

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A particular type of epilepsy in children with congenital hemiparesis associated with unilateral polymicrogyria

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Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

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Bilateral generalized polymicrogyria (BGP): a distinct syndrome of cortical malformation

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Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome

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Bilateral parasagittal parietooccipital polymicrogyria and epilepsy

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Congenital bilateral perisylvian syndrome: study of 31 patients. The CBPS Multicenter Collaborative Study

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Unlayered polymicrogyria : structural and developmental aspects

21 January 2018

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Polymicrogyria includes fusion of the molecular layer and decreased neuronal populations but normal cortical laminar organization

21 January 2018

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Arthrogryposis multiplex congenita and bilateral parietal polymicrogyria in association with the intrauterine death of a twin

21 January 2018

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Monozygous twin with polymicrogyria and normal co-twin

21 January 2018

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Five children with del (2)(q31q33) and one individual with dup (2)(q31q33) from a single family: review of brain, cardiac, and limb malformations

21 January 2018

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Clinical, MRI, and pathological features of polymicrogyria in chromosome 22q11 deletion syndrome.

21 January 2018

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Polymicrogyria with dysmorphic basal ganglia? Think tubulin!

21 January 2018

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Recessive LAMC3 mutations cause malformations of occipital cortical development

21 January 2018

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Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria

21 January 2018

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TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria

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RTTN mutations link primary cilia function to organization of the human cerebral cortex

21 January 2018

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WDR62 is associated with the spindle pole and is mutated in human microcephaly

21 January 2018

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Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria

21 January 2018

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).

21 January 2018

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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

21 January 2018

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Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria

21 January 2018

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Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responses.

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Neuroimaging of ventriculomegaly in the fetal period

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Fetal magnetic resonance imaging and three-dimensional ultrasound in clinical practice: general aspects

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Megalencephaly syndromes and activating mutations in the PI3K-AKT pathway: MPPH and MCAP.

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Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

21 January 2018

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COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans

21 January 2018

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Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly

21 January 2018

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We have got you 'covered': how the meninges control brain development

21 January 2018

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Experimentally induced focal microgyria and status verrucosus deformis in rats--pathogenesis and interrelation. Histological and autoradiographical study

21 January 2018

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Experimentally induced laminar necrosis, status verrucosus, focal cortical dysplasia reminiscent of microgyria, and porencephaly in the rat.

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Regulation of radial glial survival by signals from the meninges.

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GPR56 regulates pial basement membrane integrity and cortical lamination

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Primary cortical folding in the human newborn: an early marker of later functional development

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Mapping the early cortical folding process in the preterm newborn brain

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Complication begets clarification in classification

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Development of the cortical dysplasia of type II lissencephaly

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Early formative stage of human focal cortical gyration anomalies: fetal MRI.

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Identifiers

DOI

10.1111/DMCN.12840

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15 March 2018

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15 March 2018