(Q30558796)

12 August 2017

Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis (English)

1 reference

12 August 2017

0 references

17

1 reference

24 June 2017

Elena Parrini

6

0 references

Stephen Robertson

Stephen Robertson

9

0 references

Ingrid Scheffer

Ingrid E Scheffer

5

0 references

Samuel Berkovic

Samuel F Berkovic

16

0 references

Renzo Guerrini

18

Renzo Guerrini

1 reference

12 August 2017

11

Felix Rosenow

1 reference

12 August 2017

3

Richard J Leventer

1 reference

12 August 2017

10

Gaetano Tortorella

1 reference

12 August 2017

14

Eva Andermann

1 reference

12 August 2017

Tiziana Pisano

1

1 reference

12 August 2017

A James Barkovich

2

1 reference

12 August 2017

Waney Squier

4

1 reference

12 August 2017

Susan Blaser

7

1 reference

12 August 2017

Carla Marini

8

1 reference

12 August 2017

Pierre Thomas

12

1 reference

12 August 2017

George McGillivray

13

1 reference

12 August 2017

Frederick Andermann

15

1 reference

12 August 2017

language of work or name

English

0 references

publication date

22 August 2012

1 reference

12 August 2017

1 reference

12 August 2017

79

1 reference

12 August 2017

12

1 reference

12 August 2017

1244-1251

1 reference

Psychiatry, neurology, and the role of the cerebellum

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Expression of the homeobox genes OTX2 and OTX1 in the early developing human brain

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

The autism susceptibility gene met regulates zebrafish cerebellar development and facial motor neuron migration

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Morphological spectrum of prenatal cerebellar disruptions

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

GPR56 regulates pial basement membrane integrity and cortical lamination

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Periventricular nodular heterotopia with overlying polymicrogyria

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Periventricular heterotopia: new insights into Ehlers-Danlos syndrome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

A developmental and genetic classification for malformations of cortical development

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

X-linked malformations of neuronal migration

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

MRI analysis of sulcation morphology in polymicrogyria

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Identification of region-specific transcription factor genes in the adult mouse brain by medium-scale real-time RT-PCR.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

A rationale for degrees of retardation.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Brain structural abnormalities in young children with autism spectrum disorder.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

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

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Hippocampal developmental changes in patients with partial epilepsy: magnetic resonance imaging and clinical aspects.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440449

Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis

26 November 2018

1 reference

12 December 2020

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

1 reference

12 December 2020

Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females

1 reference

12 December 2020

Germline and mosaic mutations of FLN1 in men with periventricular heterotopia

1 reference

12 December 2020

10.1212/WNL.0B013E31826AAC88

Identifiers

DOI

1 reference

12 August 2017

1 reference

12 August 2017

1 reference