(Q35788517)

10 August 2017

Red-green color vision impairment in Duchenne muscular dystrophy (English)

1 reference

10 August 2017

4

Mayana Zatz

1 reference

PubMed ID

17503325

10 August 2017

Claudia Feitosa-Santana

Claudia Feitosa-Santana

3

0 references

Marcelo F Costa

Marcelo Fernandes Costa

1

0 references

Dora F. Ventura

Dora Fix Ventura

Andre Gustavo Fernandes Oliveira

5

0 references

2

Andre Gustavo Fernandes Oliveira

1 reference

PubMed ID

17503325

10 August 2017

language of work or name

English

0 references

publication date

13 April 2007

1 reference

American Journal of Human Genetics

10 August 2017

1 reference

10 August 2017

80

1 reference

10 August 2017

1064-1075

1 reference

10 August 2017

6

1 reference

Normal photoresponses and altered b-wave responses to APB in the mdx(Cv3) mouse isolated retina ERG supports role for dystrophin in synaptic transmission

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Multifocal and full-field electroretinogram changes associated with color-vision loss in mercury vapor exposure.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Paths to colour in the retina

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Simultaneous comparison of relative damage to chromatic pathways in ocular hypertension and glaucoma: correlation with clinical measures

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Colour coding in the primate retina: diverse cell types and cone-specific circuitry

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Preterm birth and visual development

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Dystrophin and muscular dystrophy: past, present, and future

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Correlation between electroretinographic findings, clinical phenotypic and genotypic analysis in Duchenne and Becker muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Characterization of the intermolecular associations of the dystrophin-associated glycoprotein complex in retinal Müller glial cells

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

What covariance mechanisms underlie green/red equiluminance, luminance contrast sensitivity and chromatic (green/red) contrast sensitivity?

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Molecular genetics of color vision and color vision defects

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Some transformations of color information from lateral geniculate nucleus to striate cortex

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Expression of Dp71 in Müller glial cells: a comparison with utrophin- and dystrophin-associated proteins.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

12 July 2018

Dystrophin in the retina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Localization of dystrophin and beta-dystroglycan in bovine retinal photoreceptor processes extending into the postsynaptic dendritic complex

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Duchenne/Becker muscular dystrophy: from molecular diagnosis to gene therapy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Carrier detection in Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

The X-Chrom lens. On seeing red.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Analysis of Response Patterns of LGN Cells*

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Colour vision and contrast sensitivity losses of mercury intoxicated industry workers in Brazil.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Absence of binocular summation, eye dominance, and learning effects in color discrimination.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

L and M cone contributions to the midget and parasol ganglion cell receptive fields of macaque monkey retina.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Dystrophin Dp71 is critical for the clustered localization of potassium channels in retinal glial cells.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Extra-muscle involvement in dystrophinopathies: an electroretinography and evoked potential study.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

A novel dystrophin isoform is required for normal retinal electrophysiology.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Exon–Intron Organization of the Human Dystrophin Gene

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1867095

Electroretinogram in Duchenne/Becker muscular dystrophy

15 November 2018

1 reference

12 December 2020

Diagnosis of progressive muscular dystrophy

1 reference

12 December 2020

Colour discrimination thresholds in Parkinson's disease: results obtained with a rapid computer-controlled colour vision test

1 reference

12 December 2020

Immunocytochemical study of dystrophin-related protein in the rat retina

1 reference

12 December 2020

Variation of chromatic sensitivity across the life span

1 reference

12 December 2020

Colour discrimination ellipses in patients with dominant optic atrophy

1 reference

12 December 2020

The effects of dystrophin gene mutations on the ERG in mice and humans

1 reference

12 December 2020

Dystrophin and the dystrophin-associated glycoprotein, beta-dystroglycan, co-localize in photoreceptor synaptic complexes of the human retina

1 reference

12 December 2020

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

1 reference

12 December 2020

mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy

1 reference

12 December 2020

Duchenne muscular dystrophy: negative scotopic bright-flash electroretinogram and normal dark adaptation

1 reference

12 December 2020

Dystrophin in rod spherules; submembranous dense regions facing bipolar cell processes

1 reference

12 December 2020

Luminance noise and the rapid determination of discrimination ellipses in colour deficiency

1 reference

12 December 2020

Genotype and electroretinal heterogeneity in Duchenne muscular dystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1086/518127

1 reference

10 August 2017

1 reference

10 August 2017

1 reference

PubMed ID

17503325