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Last Updated: 01/07/2026

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Found 382 publications

A Novel Frameshift Variant in KIF11 Causes Autosomal Dominant Familial Exudative Vitreoretinopathy in a Chinese Family.

A Novel Frameshift Variant in KIF11 Causes Autosomal Dominant Familial Exudative Vitreoretinopathy in a Chinese Family.

Journal: Genetic testing and molecular biomarkers
Published: December 04, 2025

A novel TSPAN12 mutation causing retinitis pigmentosa-like appearance of familial exudative vitreoretinopathy.

A novel TSPAN12 mutation causing retinitis pigmentosa-like appearance of familial exudative vitreoretinopathy.

Journal: Ophthalmic genetics
Published: November 20, 2025

Late Reactivation of Retinopathy in a Treatment-Naive Female Adult Patient With History of Prematurity and ZNF408 Mutation.

Late Reactivation of Retinopathy in a Treatment-Naive Female Adult Patient With History of Prematurity and ZNF408 Mutation.

Journal: Journal of vitreoretinal diseases
Published: November 20, 2025

Schisis-Like Presentations of Familial Exudative Vitreoretinopathy Caused by FZD4 Mutations.

Schisis-Like Presentations of Familial Exudative Vitreoretinopathy Caused by FZD4 Mutations.

Journal: Journal of vitreoretinal diseases
Published: November 17, 2025

Severe Exudative Vitreoretinopathy Secondary to Homozygous PCDH12 Mutations.

Severe Exudative Vitreoretinopathy Secondary to Homozygous PCDH12 Mutations.

Journal: Retinal cases & brief reports
Published: November 07, 2025

Efficacy and Vascular Redevelopment of Anti-vascular Endothelial Growth Factor Therapy for Stage 2 early-diagnosed Familial Exudative Vitreoretinopathy.

Efficacy and Vascular Redevelopment of Anti-vascular Endothelial Growth Factor Therapy for Stage 2 early-diagnosed Familial Exudative Vitreoretinopathy.

Journal: Retina (Philadelphia, Pa.)
Published: November 06, 2025

Rigid gas permeable contact lens correction for young children with special refractive errors.

Rigid gas permeable contact lens correction for young children with special refractive errors.

Journal: Clinical & experimental optometry
Published: October 27, 2025

KIF11-related MCLMR presenting with FEVR-like retinopathy: first report in an Indian child.

KIF11-related MCLMR presenting with FEVR-like retinopathy: first report in an Indian child.

Journal: Ophthalmic genetics
Published: October 09, 2025

Feasibility of Multimodal Deep Learning for Automated Staging of Familial Exudative Vitreoretinopathy Using Color Fundus Photographs and Fluorescein Angiography.

Feasibility of Multimodal Deep Learning for Automated Staging of Familial Exudative Vitreoretinopathy Using Color Fundus Photographs and Fluorescein Angiography.

Journal: Diagnostics (Basel, Switzerland)
Published: October 08, 2025

Refractive Error Correction With Glasses in Congenital Ocular Fundus Anomalies: A Retrospective Series of 18 Children With Different Disease Entities Followed Up for More Than 10 Years.

Refractive Error Correction With Glasses in Congenital Ocular Fundus Anomalies: A Retrospective Series of 18 Children With Different Disease Entities Followed Up for More Than 10 Years.

Journal: Cureus
Published: October 07, 2025

A genotype to phenotype relationship of exudative vitreoretinopathy in Loeys-Dietz syndrome due to a pathogenic variant in TGFBR2.

A genotype to phenotype relationship of exudative vitreoretinopathy in Loeys-Dietz syndrome due to a pathogenic variant in TGFBR2.

Journal: Ophthalmic genetics
Published: September 30, 2025

Clinical Characteristics and Long-term Visual Prognosis of Familial Exudative Vitreoretinopathy.

Clinical Characteristics and Long-term Visual Prognosis of Familial Exudative Vitreoretinopathy.

Journal: American journal of ophthalmology
Published: September 20, 2025
Showing 1-12 of 382

Last Updated: 01/07/2026