The aim of this review article is to describe the specific features of Stargardt disease and ABCA4 retinopathies (ABCA4R) using multimodal imaging and functional testing and to highlight their relevance to potential therapeutic interventions. Standardised measures of tissue loss, tissue function and rate of change over time using formal structured deep phenotyping in Stargardt disease and ABCA4R are key in diagnosis, and prognosis as well as when selecting cohorts for therapeutic intervention. In addition, a meticulous documentation of natural history will be invaluable in the future to compare treated with untreated retinas. Despite the familiarity with the term Stargardt disease, this eponymous classification alone is unhelpful when evalu...
PURPOSE. Stargardt disease (STGD1). the most common early-onset recessive macular degeneration, is c...
Background: Stargardt disease (STGD) is the most common juvenile hereditary macular dystrophy. In th...
Stargardt disease is caused by mutations in the ABCA4 gene and is probably the commonest inherited c...
PURPOSE: To perform a clinical characterization of Stargardt patients with ABCA4 gene mutation, and ...
Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotyp...
BACKGROUND: Each inherited retinal disorder is rare, but together, they affect millions of people wo...
Purpose: To investigate phenotypic variability in terms of best-corrected visual acuity (BCVA) in pa...
BackgroundEach inherited retinal disorder is rare, but together, they affect millions of people worl...
Purpose: The purpose of our study was to investigate morpho-functional features of the preferred ret...
<p><i>Background</i>: The goal of this study was to define the histopathology of the retina in donor...
Stargardt disease (STGD1) and ABCA4 retinopathies (ABCA4R) are caused by pathogenic variants in the ...
Purpose: To assess retinal function in combination with the retinal structure in ABCA4-associated re...
Stargardt disease (STGD1; MIM 248200) is the most common inherited macular dystrophy in both adults ...
BACKGROUND: The majority of studies on the retina-specific ATP-binding cassette transporter (ABCA4) ...
[EN] Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phe...
PURPOSE. Stargardt disease (STGD1). the most common early-onset recessive macular degeneration, is c...
Background: Stargardt disease (STGD) is the most common juvenile hereditary macular dystrophy. In th...
Stargardt disease is caused by mutations in the ABCA4 gene and is probably the commonest inherited c...
PURPOSE: To perform a clinical characterization of Stargardt patients with ABCA4 gene mutation, and ...
Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotyp...
BACKGROUND: Each inherited retinal disorder is rare, but together, they affect millions of people wo...
Purpose: To investigate phenotypic variability in terms of best-corrected visual acuity (BCVA) in pa...
BackgroundEach inherited retinal disorder is rare, but together, they affect millions of people worl...
Purpose: The purpose of our study was to investigate morpho-functional features of the preferred ret...
<p><i>Background</i>: The goal of this study was to define the histopathology of the retina in donor...
Stargardt disease (STGD1) and ABCA4 retinopathies (ABCA4R) are caused by pathogenic variants in the ...
Purpose: To assess retinal function in combination with the retinal structure in ABCA4-associated re...
Stargardt disease (STGD1; MIM 248200) is the most common inherited macular dystrophy in both adults ...
BACKGROUND: The majority of studies on the retina-specific ATP-binding cassette transporter (ABCA4) ...
[EN] Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phe...
PURPOSE. Stargardt disease (STGD1). the most common early-onset recessive macular degeneration, is c...
Background: Stargardt disease (STGD) is the most common juvenile hereditary macular dystrophy. In th...
Stargardt disease is caused by mutations in the ABCA4 gene and is probably the commonest inherited c...