Hereditary macular dystrophy

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1975-2016
0119752016

Papers overview

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2016
2016
PURPOSE To assess the etiology, clinical features, and outcome of choroidal neovascularization (CNV) in children. METHODS We… (More)
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Review
2009
Review
2009
Untreatable hereditary macular dystrophy (HMD) presents a major burden to society in terms of the resulting patient disability… (More)
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2001
2001
PURPOSE To report a new North American family with dominant radial drusen and Arg345Trp mutation in the EFEMP1 gene. METHODS… (More)
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1998
1998
Background: North Carolina macular dystrophy (NCMD) is a rare autosomal dominant maculopathy with highly variable expressivity… (More)
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Review
1996
Review
1996
PURPOSE To clarify the nosology of autosomal dominant central areolar pigment epithelial dystrophy (CAPED) as previously… (More)
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1985
1985
The enzyme activities of acid phosphatase, beta-glucuronidase, N-acetyl-beta-D-glucosaminidase, and alpha-D-mannosidase were not… (More)
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1983
1983
Chloroquine retinopathy is a well-documented toxic manifestation of a commonly used systemic medication. The major retinal… (More)
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1975
1975
A family with a unique hereditary macular dystrophy is presented. The disorder is transmitted as an autosomal dominant trait… (More)
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