• A case of exudative vitreoretinopathy and chorioretinal coloboma associated with microcephaly in a female with contiguous Xp11.3-11.4 deletion
• An essential role of the cysteine-rich domain of FZD4 in Norrin/Wnt signaling and familial exudative vitreoretinopathy
• Asymmetric familial exudative vitreoretinopathy in a premature infant misdiagnosed as retinopathy of prematurity
• Avascular Peripheral Retina in Infants
• Challenges in posterior uveitis-tips and tricks for the retina specialist
• Clinical characteristics and surgical management of familial exudative vitreoretinopathy-associated rhegmatogenous retinal detachment
• Familial exudative vitreoretinopathy
• Familial Exudative Vitreoretinopathy and Systemic Abnormalities in Patients With CTNNB1 Mutations
• Familial exudative vitreoretinopathy simulating Coats disease: case report
• Familial exudative vitreoretinopathy with an anterior segment vasoproliferative mass
• FEVR phenotype associated with septo-optic dysplasia
• FEVR-like Presentation in an 11q Deletion Syndrome and 16p13.11 Microdeletion
• Long term clinical outcomes and genotype-phenotype correlation in Familial Exudative Vitreoretinopathy in a tertiary referral center
• Long-term efficacy and complications of intravitreal anti-vascular endothelial growth factor agents combined with ablative therapies in juvenile Coats disease: a five year follow-up study
• Loss of Tbx3 in Mouse Eye Causes Retinal Angiogenesis Defects Reminiscent of Human Disease
• Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy
• Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes
• Optical Coherence Tomography Angiography in Pediatric Retinal Disorders
• Osteoporotic vertebral fractures during pregnancy: be aware of a potential underlying genetic cause
• Pattern of choroidal thickness in early-onset high myopia
• Pediatric cataract, myopic astigmatism, familial exudative vitreoretinopathy and primary open-angle glaucoma co-segregating in a family
• Peripheral and central retinal vascular changes in asymptomatic family members of patients with familial exudative vitreoretinopathy
• Phenotype-Based Genetic Analysis Reveals Missing Heritability of <em>KIF11</em>-Related Retinopathy: Clinical and Genetic Findings
• Quantitative Analysis of Vascular Abnormalities in Full-Term Infants With Mild Familial Exudative Vitreoretinopathy
• Ultra-widefield imaging for the management of pediatric retinal diseases
• Vascular features around the optic disc in familial exudative vitreoretinopathy: findings and their relationship to disease severity
• Vitreoretinopathy-Associated Pediatric Retinal Detachment Treatment Outcomes: IRIS® Registry (Intelligent Research in Sight) Analysis
• Whole-Gene Deletions of <em>FZD4</em> Cause Familial Exudative Vitreoretinopathy