Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Evidence of widespread retinal dysfunction in patients with stargardt disease and morphologically unaffected carrier relatives.

Investigative ophthalmology & visual science - 1 Mar 2008

Maia-Lopes Susana, Silva Eduardo D, Silva Maria Fátima, Reis Aldina, Faria Pedro, Castelo-Branco Miguel

Abstract excerpt

PURPOSE: To characterize contrast sensitivity (CS) across the visual field for two achromatic spatial-temporal frequencies in 21 families with Stargardt disease (STGD) and to correlate psychophysical impairment with patterns of change in multifocal electroretinography (mfERG). METHODS: Twenty-sev...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to ATP-Binding Cassette Transporters
Share to Color Vision Defects
Share to Electroretinography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Carrier Screening

Share to Macular Degeneration

Share to Oligonucleotide Array Sequence Analysis

Share to Retina

Share to Visual Fields

Source

Identifiers

PMID: 18326749
DOI: 10.1167/iovs.07-1051

Genes

ABCA4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18326749-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Evidence of widespread retinal dysfunction in patients with stargardt disease and morphologically unaffected carrier relatives.PMID 18326749Read ↗

The Pattern of Retinal Ganglion Cell Loss in OPA1-Related Autosomal Dominant Optic Atrophy Inferred From Temporal, Spatial, and Chromatic Sensitivity Losses.Semantic proximity Read ↗

Multidimensional Functional Phenotyping Based on Photoreceptor-Directed Temporal Contrast Sensitivity Defects in Inherited Retinal Diseases.Semantic proximity Read ↗

New insights into Stargardt disease with multimodal imaging.Semantic proximity Read ↗

Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.Semantic proximity Read ↗

ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina.Semantic proximity Read ↗

Retinal function in best macular dystrophy: relationship between electrophysiological, psychophysical, and structural measures of damage.Semantic proximity Read ↗

Early impairment of the full-field photopic negative response in patients with Stargardt disease and pathogenic variants of the ABCA4 gene.Semantic proximity Read ↗

Peripapillary dark choroid ring as a helpful diagnostic sign in advanced stargardt disease.Semantic proximity Read ↗

Test–Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy TrialSemantic proximity Read ↗

Correlations among near-infrared and short-wavelength autofluorescence and spectral-domain optical coherence tomography in recessive Stargardt disease.Semantic proximity Read ↗

Colour Vision in Stargardt Disease.Semantic proximity Read ↗

Disruption in Bruch membrane in patients with Stargardt disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.