Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders (Q30480684)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Visual phenotype in Williams-Beuren syndrome challenges magnocellular theories explaining human neurodevelopmental visual cortical disorders	scientific article

Statements

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

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q30480684&oldid=1975331919"