familial exudative vitreoretinopathy

familial exudative vitreoretinopathy

familial exudative vitreoretinopathy

Familial Exudative Vitreoretinopathy - an overview | Scien...
Familial exudative vitreoretinopathy (FEVR) is a bilateral disorder of aberrant peripheral retinal development, including peripheral avascular retina, abnor...
Familial Exudative Vitreoretinopathy - ScienceDirect
Familial Exudative Vitreoretinopathy Author links open overlay panelM. MadisonSlusherM.D.W.E.HuttonM.D. Previous article in issue First page previe...
Familial exudative vitreoretinopathy mimicking persistent...
Conclusions: With highly asymmetric involvement, neonatal familial exudative vitreoretinopathy can mimic persistent hyperplastic primary vitreous. Fellow eye...
A mutation in the Norrie disease gene (NDP) associated with X...
Familial exudative vitreoretinopathy (FEVR) is a hereditary disorder characterized by an abnormality of the peripheral retina. Both autosomal dominant (...
LDL-Rezeptor-related-Protein 5
Qin M et al. (2008) Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudati...
FZD4 (frizzled class receptor 4)
Note Familial Exudative Vitreoretinopathy (FEVR) is a hereditary ocular disorder characterized by incomplete development of the retinal vasculature. It is pos...
Archive - Nature Genetics
A mutation in the Norrie disease gene (NDP) associated with X−linked familial exudative vitreoretinopathy Z-Y. Chen, E.M. Battinelli, A. Fielder, S. Bundey, ...
Genetic susceptibility to advanced retinopathy of prematurity (...
Molecular genetics of Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematurity. In In retinal degeneration: causes, diagnosis and treat...
FZD4 - Frizzled-4 precursor - Homo sapiens (Human) - FZD4 g...
Orphaneti 891Familial exudative vitreoretinopathy 91495Persistent hyperplastic primary vitreous 90050Retinopathy of prematurity Polymorphism and mutation...
LRP5 (low density lipoprotein receptor-related protein 5)
Schematic representation of LRP5 mutations; those associated with osteoporosis pseudoglioma (OPPG) syndrome, autosomal-dominant familial exudative vi...