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

Clinical phenotype as a prognostic factor in Stargardt disease.

Retina (Philadelphia, Pa.) - 1 Apr 2004

Oh Kean T, Weleber Richard G, Oh Dawn M, Billingslea Andrea M, Rosenow Justin, Stone Edwin M

Abstract excerpt

PURPOSE: To determine the prognostic significance of widespread flecks, described as fundus flavimaculatus, in patients with Stargardt disease. DESIGN: Historical cohort study. SUBJECTS AND METHODS: Patients with Stargardt disease were identified by searching preexisting databases at the University of Iowa and Oregon Health Sciences University. The medical records of these patients were evaluated for the validity...

Read the complete abstract on PubMed

Topics

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

Share to Prognosis
Share to Life Tables
Share to Macular Degeneration

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Cohort Studies

Share to Fundus Oculi

Share to Infant

Share to Survival Analysis

Share to Visual Acuity

Source

Identifiers

PMID: 15097887
DOI: 10.1097/00006982-200404000-00011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical phenotype as a prognostic factor in Stargardt disease.PMID 15097887Read ↗

Early-onset stargardt disease: phenotypic and genotypic characteristics.Semantic proximity Read ↗

ASSOCIATION BETWEEN GENOTYPE AND DISEASE PROGRESSION IN ITALIAN STARGARDT PATIENTS: A Retrospective Natural History Study.Semantic proximity Read ↗

Clinical phenotypes and prognostic full-field electroretinographic findings in Stargardt disease.Semantic proximity Read ↗

Study of Late-Onset Stargardt Type 1 DiseaseSemantic proximity Read ↗

A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlations.Semantic proximity Read ↗

Clinical and molecular analysis of Stargardt disease with preserved foveal structure and function.Semantic proximity Read ↗

Predictors of visual acuity and genotype-phenotype correlates in a cohort of patients with Stargardt disease.Semantic proximity Read ↗

Foveal sparing in Stargardt disease.Semantic proximity Read ↗

The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.Semantic proximity Read ↗

Loss of peripapillary sparing in non-group I Stargardt disease.Semantic proximity Read ↗

Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus.Semantic proximity Read ↗

Natural history of phenotypic changes in Stargardt macular dystrophy.Semantic proximity Read ↗

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