(Q37841670)

24 August 2017

title

The clinical spectrum of nodular heterotopias in children: report of 31 patients (English)

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24 August 2017

9

Lionel Carmant

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24 August 2017

8

Jacques Michaud

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24 August 2017

Myriam Srour

1

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24 August 2017

Marie-France Rioux

2

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24 August 2017

Caroline Varga

3

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24 August 2017

Anne Lortie

4

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24 August 2017

Philippe Major

5

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24 August 2017

Yves Robitaille

6

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24 August 2017

Jean-Claude Décarie

7

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24 August 2017

language of work or name

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14 February 2011

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24 August 2017

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24 August 2017

volume

52

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24 August 2017

issue

4

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24 August 2017

page(s)

728-737

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Periventricular nodular heterotopia: epileptogenic findings.

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Periventricular nodular heterotopia: classification, epileptic history, and genesis of epileptic discharges.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Movement disorder and neuronal migration disorder due to ARFGEF2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Filamin A mutation, a common cause for periventricular heterotopia, aneurysms and cardiac defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Periventricular and subcortical nodular heterotopia. A study of 33 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Cocaine-induced disturbances of corticogenesis in the developing murine brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Neuronal migration disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Focal cerebral mantle disruption in fetal hydrocephalus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Mutations in the gene encoding filamin A as a cause for familial cardiac valvular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5-11.1 Mb terminal deletion of 1p36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Autosomal recessive form of periventricular heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Periventricular heterotopia associated with chromosome 5p anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

Periventricular nodular heterotopia and Williams syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2010.02975.X

10.1111/J.1528-1167.2010.02975.X

21 January 2018

Identifiers

DOI

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24 August 2017

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