Familial exudative vitreoretinopathy (FEVR) is a heritable vitreoretinopathy characterized by
anomalous retinal vascular development. The principal feature of the disease is an …

Familial exudative vitreoretinopathy (FEVR) is a hereditary ocular disorder characterized by
incomplete vascularization/abnormality of peripheral retina. Four of the identified disease …

Purpose.: Familial exudative vitreoretinopathy (FEVR) is a developmental disease that can
cause visual impairment and retinal detachment at a young age. Four genes involved in the …

Purpose The in vivo microstructural features of familial exudative vitreoretinopathy (FEVR)
have not been well described. We present new anatomic features of FEVR with functional …

Purpose: To discuss the latest advances and controversies in the diagnosis and care of
infants with retinopathy of prematurity (ROP). Methods: Literature review. Results …

Purpose: To study vascular endothelial growth factor (VEGF) regulation in the development
of intravitreous neovascularization and peripheral avascular retina in peripheral severe …

Purpose Retinopathy of prematurity (ROP) is a complex disease with a genetic
predisposition, but little is known about its genetic background. It has a clinical resemblance …

Purpose.: To determine genetic variants associated with severe retinopathy of prematurity
(ROP) in a candidate gene cohort study of US preterm infants. Methods.: Preterm infants in …

Purpose: To investigate the clinical findings in Chinese patients diagnosed with familial
exudative vitreoretinopathy (FEVR) and carrying pathogenic mutations. Methods: One …

Wnt-signaling, a ubiquitous pathway that directs differentiation, cell polarity, and tissue
specificity, has been implicated as an important gene-expression pathway in retinal …