Corneal Dystrophy, Juvenile Epithelial of Meesmann

Known as: Dystrophies, Meesmann Corneal, Corneal Dystrophies, Meesmann, Juvenile epithelial corneal dystrophy 
An autosomal dominant inherited corneal disorder caused by mutations in the KRT3 and KRT12 genes. It is characterized by the formation of multiple… (More)
National Institutes of Health

Papers overview

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Review
2013
Review
2013
The main treatment available for restoration of the corneal endothelium is keratoplasty. This procedure is faced with several… (More)
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2010
2010
BACKGROUND Mutations in COL8A2 gene which encodes the collagen alpha-2 (VIII) chain have been identified in both familial and… (More)
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Highly Cited
2008
Highly Cited
2008
The endothelial (posterior) corneal dystrophies, which result from primary endothelial dysfunction, include Fuchs endothelial… (More)
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Highly Cited
2008
Highly Cited
2008
The centriole is the core structure of centrosome and cilium. Failure to restrict centriole duplication to once per cell cycle… (More)
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2006
2006
PURPOSE To investigate the genetic basis of late-onset, familial Fuchs endothelial corneal dystrophy (FECD) through screening of… (More)
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2004
2004
OBJECTIVE We analyzed laboratory results from corneal ulcers seen from 1976 to 1999 at the Francis I. Proctor Foundation, a… (More)
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2000
2000
PURPOSE The authors describe the clinicopathologic features of three patients with adult onset foveomacular pigment epithelial… (More)
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1998
1998
PURPOSE To report a family with several members affected with granular corneal dystrophy Groenouw type 1. Three members of the… (More)
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1997
1997
Keratin 12 (K12) is an intermediate-filament protein expressed specifically in corneal epithelium. Recently, we isolated K12 cDNA… (More)
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1980
1980
Thirty-three pateints had adult-onset foveomacular dystrophy. The macular lesions typically resulted in a mild to moderate… (More)
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