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Avellino corneal dystrophy

Known as: CDA, Granular and lattice corneal dystrophies, ACD 
 
National Institutes of Health

Papers overview

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2013
2013
The hallmark of granular corneal dystrophy type 2 (GCD2) is the deposit of mutant transforming growth factor-β (TGF-β)-induced… Expand
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2011
2011
PURPOSE. The purpose of this study was to investigate the effects and molecular mechanisms of lithium on inhibition of TGFBIp… Expand
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2009
2009
Granular corneal dystrophy type II (GCD II) is an autosomal dominant disorder characterized by age-dependent progressive… Expand
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2009
2009
Purpose To characterize the clinical phenotype, histopathological features, and molecular genetic basis of an Avellino corneal… Expand
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2009
2009
PURPOSE To report a case of Avellino corneal dystrophy (ACD) in a patient of Indian origin treated with femtosecond-assisted… Expand
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2008
2008
PURPOSE To analyze components of the deposits in the corneal flap interface of granular corneal dystrophy type II (GCD II… Expand
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2007
2007
PURPOSE To describe the clinical features of homozygous granular corneal dystrophy type II (GCDII) with age and with several… Expand
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2001
2001
PURPOSE Mutations in the BIGH3 gene on chromosome 5q31 cause four distinct autosomal dominant corneal dystrophies. We sought to… Expand
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2000
2000
PURPOSE To investigate mutations of the human transforming growth factor beta-induced gene (TGFBI), transforming growth factor… Expand
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2000
2000
Purpose. To investigate corneal deposits associated with kerato-epithelin (KE) in three corneal dystrophies harboring mutations… Expand
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