Major advances in the study of inherited retinal diseases (IRDs) have placed efforts to
develop treatments for these blinding conditions at the forefront of the emerging field of …

Stargardt macular dystrophy (Stargardt disease; STGD1; OMIM 248200) is the most
prevalent inherited macular dystrophy. STGD1 is an autosomal recessive disorder caused …

Importance Sensitive outcome measures for disease progression are needed for treatment
trials of Stargardt disease. Objective To estimate the progression rate of atrophic lesions in …

Purpose To determine the reliability and repeatability of quantitative evaluation of areas of
decreased autofluorescence (DAF) from fundus autofluorescence (FAF) images and track …

Purpose To explore fundus autofluorescence (FAF) imaging as an alternative to
electroretinography as a noninvasive, quick, and readily interpretable method to predict …

Purpose: To define unmet needs in ophthalmology that can realistically be addressed in the
next 5 years (2019–2025) and describe potential avenues for research to address these …

Inherited retinal dystrophies (IRDs) are bilateral genetic conditions of the retina, leading to
irreversible vision loss. This study included 55 eyes afflicted with IRDs affecting the macula …

Purpose To investigate lipofuscin-related quantitative autofluorescence measures and their
association with demographic characteristics, retinal structure, retinal function and genotype …

Abstract The Progression of Atrophy Secondary to Stargardt Disease (ProgStar) studies
were designed to measure the progression of Stargardt disease through the use of fundus …

Purpose To compare full-field stimulus (FST) threshold values to conventional functional and
anatomical measures commonly used in clinical practice. Design Cross-sectional study …