Skip to search formSkip to main contentSkip to account menu

VITREORETINOCHOROIDOPATHY (disorder)

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Mutations in BEST1, the gene encoding for Bestrophin-1 (Best1), cause five, clinically distinct inherited retinopathies: Best… 
Review
2008
Review
2008
1. Thirkill CE, Fitzgerald P, Sergott RC, Roth AM, Tyler NK, Kaltner JL. Cancerassociated retinopathy (CAR-syndrome) with… 
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… 
2005
2005
ZusammenfassungDie Best’sche vitelliforme Makuladystrophie (Morbus Best) ist eine autosomal dominante Erkrankung der zentralen… 
2005
2005
This paper describes a new MAC protocol for integrated inter-vehicle and road to vehicle communications called VRCP (Vehicle and… 
1998
1998
Abstract • Background: Autosomal dominant vitreoretinochoroidopathy (ADVIRC) is a rare disorder previously described in four… 
1995
1995
The clinicopathologic findings were obtained from enucleated eyes, obtained post mortem, of a 26-year-old woman with autosomal…