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VITREORETINOCHOROIDOPATHY (disorder)

Known as: Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos, Vitreoretinochoroidopathy With Microcornea, Glaucoma, And Cataract, Vitreoretinochoroidopathy, Autosomal Dominant 
National Institutes of Health

Papers overview

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Review
2011
Review
2011
PurposeTo describe the spectrum of phenotypic characteristics of BEST1-related autosomal dominant vitreoretinochoroidopathy… 
Review
2006
Review
2006
Mutations in VMD2, encoding bestrophin (best-1), cause Best vitelliform macular dystrophy (BMD), adult-onset vitelliform macular… 
Highly Cited
2006
Highly Cited
2006
Mutations in human bestrophin-1 (VMD2) are genetically linked to a juvenile form of macular degeneration and autosomal dominant… 
Highly Cited
2004
Highly Cited
2004
PURPOSE To investigate the genetic basis of autosomal dominant vitreoretinochoroidopathy (ADVIRC), a rare, inherited retinal… 
2001
2001
Abstract.Purpose: To report the clinical and electrophysiological findings in a three-generation pedigree with autosomal dominant… 
1992
1992
Thirteen members of a family presumed to be harboring the gene for autosomal dominant vitreoretinochoroidopathy were examined. In… 
1984
1984
We report the second family recognised to have autosomal dominant vitreoretinochoroidopathy. The clinical features were (1…