Pei-liang Wu - Publications

Visual and refractive outcomes of retinopathy of prematurity in school-age patients.

Journal: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie

Published: April 11, 2026

Epidemiology and treatment trends of retinopathy of prematurity: a multi-center study involving four Asian centers and one European center (2016-2023).

Journal: Japanese journal of ophthalmology

Published: November 19, 2025

Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene Therapy.

Journal: Investigative ophthalmology & visual science

Published: September 09, 2025

Retinopathy of prematurity epidemiology and treatment trend in a tertiary medical center in Taiwan: From 2016 to 2023.

Journal: Taiwan journal of ophthalmology

Published: May 04, 2025

Advancements in ocular blood flow imaging: Clinical applications of laser speckle flowgraphy and optical coherence tomography angiography in retinal and choroidal vascular diseases.

Journal: Survey of ophthalmology

Published: April 10, 2025

Associations of PEDF genetic polymorphisms with retinopathy of prematurity.

Journal: Experimental eye research

Published: October 07, 2024

ADMINISTERING INTRAVITREAL BEVACIZUMAB FOR RETINOPATHY OF PREMATURITY: 8-Year Cognitive Outcomes In A Prospective Cohort.

Journal: Retina (Philadelphia, Pa.)

Published: August 09, 2024

Cross-Sectional Analysis of Outer Retinal Tubulation in Inherited Retinal Diseases: A Multicenter Study.

Journal: American journal of ophthalmology

Published: April 03, 2024

A GUCY2D variant associated cone-rod dystrophy with electronegative ERG: A case report and review.

Journal: American journal of ophthalmology case reports

Published: January 03, 2024

Clinical Characteristics and Genetic Variants in Taiwanese Patients With PROM1-Related Inherited Retinal Disorders.

Journal: Investigative ophthalmology & visual science

Published: November 17, 2023

Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29.

Journal: BMC medical genomics

Published: October 27, 2023

The Value of Electroretinography in Identifying Candidate Genes for Inherited Retinal Dystrophies: A Diagnostic Guide.

Journal: Diagnostics (Basel, Switzerland)

Published: August 20, 2023