(Q34320039)

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Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype

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scholarly article

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Europe PubMed Central

PubMed publication ID

1 August 2017

Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype (English)

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Europe PubMed Central

PubMed publication ID

1 August 2017

diffusion tensor imaging

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based on heuristic

inferred from title

14

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1 August 2017

Enza Maria Valente

8

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Enza Maria Valente

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13

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Ronen Spiegel

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Sabina Barresi

6

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object named as

Ginevra Zanni

2

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Duccio M. Cordelli

object named as

Duccio Maria Cordelli

5

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Carlo Cosimo Quattrocchi

object named as

Carlo C Quattrocchi

1

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Nicola Specchio

object named as

Nicola Specchio

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4

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Daniela Longo

1 reference

Europe PubMed Central

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1 August 2017

Francesco Randisi

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Francesco Randisi

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1 August 2017

Giuseppina Vitiello

12

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Giuseppina Vitiello

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1 August 2017

author name string

Antonio Napolitano

3

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1 August 2017

Tommaso Verdolotti

9

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1 August 2017

Elisabetta Genovese

10

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1 August 2017

Bruno Bernardi

15

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1 August 2017

publication date

30 December 2012

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1 August 2017

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1 August 2017

14

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1 August 2017

1

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1 August 2017

77-83

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PubMed publication ID

1 August 2017

A developmental and genetic classification for midbrain-hindbrain malformations

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Cellular and molecular biology of orphan G protein-coupled receptors

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

GPR56 regulates pial basement membrane integrity and cortical lamination

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex.

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Disease-associated GPR56 mutations cause bilateral frontoparietal polymicrogyria via multiple mechanisms

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Disease-associated mutations prevent GPR56-collagen III interaction

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Loss of Col3a1, the gene for Ehlers-Danlos syndrome type IV, results in neocortical dyslamination

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

1 reference

https://api.crossref.org/works/10.1007%2FS10048-012-0352-7

21 January 2018

Identifiers

10.1007/S10048-012-0352-7

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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