STARGARDT DISEASE 1 (disorder)

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

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Topic mentions per year

1964-2017
051019642017

Papers overview

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Highly Cited
2004
Highly Cited
2004
PURPOSE To quantify autofluorescence (AF) levels in patients with Stargardt macular dystrophy-fundus flavimaculatus (STGD-FFM… (More)
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Highly Cited
2003
Highly Cited
2003
Genetic variation in the ABCR (ABCA4) gene has been associated with five distinct retinal phenotypes, including Stargardt disease… (More)
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Highly Cited
2000
Highly Cited
2000
The photoreceptor cell-specific ATP-binding cassette transporter gene (ABCA4; previously denoted "ABCR") is mutated, in most… (More)
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Highly Cited
1999
Highly Cited
1999
Mutation scanning and direct DNA sequencing of all 50 exons of ABCR were completed for 150 families segregating recessive… (More)
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Highly Cited
1999
Highly Cited
1999
OBJECTIVE To report the spectrum of ophthalmic findings in patients with Stargardt dystrophy or fundus flavimaculatus who have a… (More)
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Highly Cited
1997
Highly Cited
1997
Stargardt disease (STGD, also known as fundus flavimaculatus; FFM) is an autosomal recessive retinal disorder characterized by a… (More)
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Highly Cited
1997
Highly Cited
1997
Highly Cited
1997
OBJECTIVE To document the deviation from normal of fundus autofluorescence in patients with inherited macular dystrophies… (More)
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Highly Cited
1993
Highly Cited
1993
BACKGROUND AND OBJECTIVES Mutations of the peripherin/RDS gene have been reported in autosomal dominant retinitis pigmentosa… (More)
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Highly Cited
1980
Highly Cited
1980
Light, fluorescent, and scanning and transmission electron microscopic examinations of two postmortem eyes from a 24-year-old man… (More)
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