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STARGARDT DISEASE 1 (disorder)

Known as: Fundus Flavimaculatus, Macular Dystrophy With Flecks, Type 1, Stargardt disease 1 
National Institutes of Health

Papers overview

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2018
2018
Stargardt disease (STGD1, OMIM 248200) is a common hereditary juvenile or early adult onset macular degeneration. It ultimately… 
Review
2017
Review
2017
The accessible and immune-privileged environment of the eye makes it ideal for gene therapy. It has been 8 years since successful… 
2009
2009
Aim: To describe a patient with type 3 choroidal neovascularization (CNV) associated with fundus flavimaculatus (FFM), who… 
2005
2005
The current issue presents a paper in which Klevering et al. see DOI 10.1007/s00417-004-1079-4 report on further cases to support… 
2004
2004
Purpose: To determine the prognostic significance of widespread flecks, described as fundus flavimaculatus, in patients with… 
1997
1997
Patients with Stargardt's disease often show a significantly reduced ability to read despite fairly good visual acuity. We… 
1989
1989
A retrospective study was performed comparing the ERG results of 15 patients with Stargardt's disease and fundus flavimaculatus… 
1982
1982
• The blood-retinal barrier was assessed by vitreous fluorophotometry in eight patients with fundus flavimaculatus (Stargardt's… 
1972
1972
In a series of three papers, Stargardt ( 1909, I93, I9I6) described with precision and thoroughness a form of hereditary macular…