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VITREORETINOCHOROIDOPATHY (disorder)
Known as:
Vitreoretinochoroidopathy, Autosomal Dominant, With Nanophthalmos
, Vitreoretinochoroidopathy With Microcornea, Glaucoma, And Cataract
, Vitreoretinochoroidopathy, Autosomal Dominant
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National Institutes of Health
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Related topics
Related topics
10 relations
Autosomal dominant inheritance
Autosomal dominant vitreoretinochoroidopathy
BEST1, VAL235ALA
BEST1, VAL86MET
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Broader (3)
Choroid Diseases
Eye Diseases, Hereditary
Retinal Degeneration
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
A virtual reality counterconditioning procedure to reduce methamphetamine cue-induced craving.
Yong-guang Wang
,
Meng-Hui Liu
,
Zhi-hua Shen
Journal of Psychiatric Research
2019
Corpus ID: 195261307
2014
2014
Disease-causing mutations associated with four bestrophinopathies exhibit disparate effects on the localization, but not the oligomerization, of Bestrophin-1.
Adiv A. Johnson
,
Yong-Suk Lee
,
+4 authors
A. Marmorstein
Experimental Eye Research
2014
Corpus ID: 7197964
Review
2011
Review
2011
BEST1-related autosomal dominant vitreoretinochoroidopathy: a degenerative disease with a range of developmental ocular anomalies
A. Vincent
,
C. Mcalister
,
C. Vandenhoven
,
E. Héon
Eye
2011
Corpus ID: 24776168
PurposeTo describe the spectrum of phenotypic characteristics of BEST1-related autosomal dominant vitreoretinochoroidopathy…
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Review
2006
Review
2006
The Light Peak of the Electroretinogram Is Dependent on Voltage-gated Calcium Channels and Antagonized by Bestrophin (Best-1)
L. Marmorstein
,
Jiang Wu
,
+10 authors
A. Marmorstein
The Journal of General Physiology
2006
Corpus ID: 14972609
Mutations in VMD2, encoding bestrophin (best-1), cause Best vitelliform macular dystrophy (BMD), adult-onset vitelliform macular…
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Highly Cited
2006
Highly Cited
2006
The Anion-Selective Pore of the Bestrophins, a Family of Chloride Channels Associated with Retinal Degeneration
Zhiqiang Qu
,
L. Chien
,
Yuan-yuan Cui
,
H. Hartzell
Journal of Neuroscience
2006
Corpus ID: 18068564
Mutations in human bestrophin-1 (VMD2) are genetically linked to a juvenile form of macular degeneration and autosomal dominant…
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Highly Cited
2004
Highly Cited
2004
Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC).
J. Yardley
,
B. Leroy
,
+18 authors
G. C. Black
Investigative Ophthalmology and Visual Science
2004
Corpus ID: 24859246
PURPOSE To investigate the genetic basis of autosomal dominant vitreoretinochoroidopathy (ADVIRC), a rare, inherited retinal…
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2003
2003
Multidetector‐Row Computed Tomography with Three‐Dimensional Volume Rendering of Pancreatic Cancer: A Complete Preoperative Staging Tool Using Computed Tomography Angiography and Volume‐Rendered…
Pamela T. Johnson
,
D. Heath
,
L. Hofmann
,
K. Horton
,
E. Fishman
Journal of computer assisted tomography
2003
Corpus ID: 25512328
&NA; Volume rendering, a postprocessing computer algorithm that creates three‐dimensional (3D) displays from computed tomography…
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2001
2001
Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree
B. Lafaut
,
Bart Loeys
,
Bart P. Leroy
,
W. Spileers
,
J. J. Laey
,
P. Kestelyn
Graefe's Archive for Clinical and Experimental…
2001
Corpus ID: 2020319
Abstract.Purpose: To report the clinical and electrophysiological findings in a three-generation pedigree with autosomal dominant…
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1992
1992
Electro-oculography in autosomal dominant vitreoretinochoroidopathy.
D. Han
,
M. F. Lewandowski
A M A Archives of Ophthalmology
1992
Corpus ID: 1193022
Thirteen members of a family presumed to be harboring the gene for autosomal dominant vitreoretinochoroidopathy were examined. In…
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1984
1984
Autosomal dominant vitreoretinochoroidopathy (ADVIRC).
N. Blair
,
M. Goldberg
,
Gerald A. Fishman
,
T. Salzano
British Journal of Ophthalmology
1984
Corpus ID: 32212710
We report the second family recognised to have autosomal dominant vitreoretinochoroidopathy. The clinical features were (1…
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