(Q30480684)

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Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Williams-Beuren syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Miguel Castelo-Branco

1

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Mafalda Mendes

2

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Ana Raquel Sebastião

3

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Aldina Reis

4

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Mário Soares

5

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Jorge Saraiva

6

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Rui Bernardes

7

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Raquel Flores

8

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Luis Pérez-Jurado

9

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Eduardo Silva

10

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

language of work or name

0 references

publication date

1 December 2007

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

117

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

12

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

3720-3729

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Motion-perception deficits and reading impairment: it's the noise, not the motion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

GTF2IRD1 in craniofacial development of humans and mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

In-depth analysis of spatial cognition in Williams syndrome: A critical assessment of the role of the LIMK1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Deficits in perceptual noise exclusion in developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

TFII-I, a candidate gene for Williams syndrome cognitive profile: parallels between regional expression in mouse brain and human phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Optical coherence tomography for ultrahigh resolution in vivo imaging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Expression of BEN, a member of TFII-I family of transcription factors, during mouse pre- and postimplantation development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Optical tomography-measured retinal nerve fiber layer thickness in normal latinos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Mutational mechanisms of Williams-Beuren syndrome deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Activity patterns in human motion-sensitive areas depend on the interpretation of global motion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

The magnocellular theory of developmental dyslexia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

I. The neurocognitive profile of Williams Syndrome: a complex pattern of strengths and weaknesses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Assessing retinal function with the multifocal technique

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Automated analysis of normal and glaucomatous optic nerve head topography images.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Characterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

A specific deficit of dorsal stream function in Williams' syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

LIM-kinase1 hemizygosity implicated in impaired visuospatial constructive cognition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Limk1 is predominantly expressed in neural tissues and phosphorylates serine, threonine and tyrosine residues in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

20 June 2018

Cortical locus of coherent motion deficits in deaf poor readers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Visual magnocellular and structure from motion perceptual deficits in a neurodevelopmental model of dorsal stream function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Motion processing specialization in Williams syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Specific retinotopically based magnocellular impairment in a patient with medial visual dorsal stream damage.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Neural basis of genetically determined visuospatial construction deficit in Williams syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Retinal origins of the primate multifocal ERG: implications for the human response

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Intact perception of biological motion in the face of profound spatial deficits: Williams syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Functional magnetic resonance imaging of early visual pathways in dyslexia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

Effect of repetitive imaging on topographic measurements of the optic nerve head

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2082146

26 November 2018

The Williams syndrome cognitive profile

1 reference

https://pubmed.ncbi.nlm.nih.gov/18037993

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Optical coherence tomography of the human retina

1 reference

https://pubmed.ncbi.nlm.nih.gov/18037993

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI32556

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

release_a4ittsxwyfchtn356jg5wxyvmu

1 reference

https://api.fatcat.wiki/v0/release/a4ittsxwyfchtn356jg5wxyvmu

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

ResearchGate publication ID

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