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Retinoschisis

Known as: Retinoschises, Retinoschisis [Disease/Finding], Retinoschisis, unspecified 
A vitreoretinal dystrophy characterized by splitting of the neuroretinal layers. It occurs in two forms: degenerative retinoschisis and X chromosome… 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Purpose: Retinoschisis and retinal detachments are primarily differentiated based on characteristic examination findings. In… 
Highly Cited
2008
Highly Cited
2008
Purpose X-linked congenital retinoschisis (RS) is a relatively frequent retinal dystrophy associated with RS1 gene mutations. A… 
Highly Cited
2003
Highly Cited
2003
A missense mutation in the mouse Col2a1 gene has been discovered, resulting in a mouse phenotype with similarities to human… 
2001
2001
PURPOSE The purpose of this study was to evaluate the hypothesis that the reduced b-wave to a-wave ratio of the brief-flash… 
Highly Cited
1999
Highly Cited
1999
The RS1 gene is the causative gene in X‐linked juvenile retinoschisis (RS). We have screened this gene for mutations in 13… 
1999
1999
X-linked retinoschisis (XLRS) is a vitreoretinal disease responsible for most cases of juvenile macular degeneration in males… 
Highly Cited
1998
Highly Cited
1998
OBJECTIVE To evaluate long-term changes in visual acuity, clinical features and complications in X-linked retinoschisis, and to… 
1977
1977
Twenty-eight eyes of 14 males affected with congenital retinoschisis were studied. The amplitude ratio of b-over a-wave (b/a… 
Review
1976
Review
1976
About 13 observations of sexe linked juvenile retinoschisis, the authors describe the ophthalmoscopic, fluorographic and… 
1964
1964
Introduction Retinoschisis is the term used to describe a split in the sensory retina. In this condition a new cleavage plane…