(Q35041227)

6 August 2017

title

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

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6 August 2017

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4

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6 August 2017

Alexander R Judkins

1

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6 August 2017

Daniel Martinez

series ordinal

2

1 reference

6 August 2017

Pamela Ferreira

series ordinal

3

1 reference

6 August 2017

Jeffrey A Golden

series ordinal

5

1 reference

6 August 2017

publication date

1 June 2011

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Journal of Neuropathology & Experimental Neurology

6 August 2017

published in

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6 August 2017

volume

70

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6 August 2017

issue

6

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6 August 2017

page(s)

438-443

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

6 August 2017

1 reference

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Abnormal development of the human cerebral cortex: genetics, functional consequences and treatment options

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Layer-specific markers as probes for neuron type identity in human neocortex and malformations of cortical development

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

SRPX2 mutations in disorders of language cortex and cognition

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

G protein-coupled receptor-dependent development of human frontal cortex

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Prenatal clastic encephalopathies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct "pseudo-TORCH" phenotype.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Interneuron deficits in patients with the Miller-Dieker syndrome

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Periventricular heterotopia may result from radial glial fiber disruption

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

Unlayered polymicrogyria : structural and developmental aspects

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3113653

10.1097/NEN.0B013E31821CCF1C

25 October 2018

Identifiers

DOI

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6 August 2017

1 reference

6 August 2017

1 reference