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Diagnostics (Basel, Switzerland)|October 14, 2023
The Value of Electroretinography in Identifying Candidate Genes for Inherited Retinal Dystrophies: A Diagnostic GuideTsai-Hsuan Yang, Eugene Yu-Chuan Kang, Pei-Hsuan Lin, et al.
American Journal of Ophthalmology Case Reports|August 5, 2024
A <i>GUCY2D</i> variant associated cone-rod dystrophy with electronegative ERG: A case report and reviewPei-Liang Wu, Pei-Hsuan Lin, Winston Lee, et al.
BMC Medical Genomics|April 19, 2024
Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29Ethan Hung-Hsi Wang, Pei-Hsuan Lin, Pei-Liang Wu, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|June 27, 2026
Visual and refractive outcomes of retinopathy of prematurity in school-age patientsYi-Hsuan Tseng, Wei-Yu Wang, Pei-Liang Wu, et al.
International Journal of Molecular Sciences|November 26, 2022
Effects of <i>TIMP-2</i> Polymorphisms on Retinopathy of Prematurity Risk, Severity, Recurrence, and Treatment ResponsePei-Liang Wu, Xiao Chun Ling, Eugene Yu-Chuan Kang, et al.
Experimental Eye Research|October 11, 2025
Associations of PEDF genetic polymorphisms with retinopathy of prematurityPei-Liang Wu, Eugene Yu-Chuan Kang, Xiao Chun Ling, et al.
Investigative Ophthalmology & Visual Science|September 9, 2025
Novel Grm6 Variant in a no b-wave (nob) Mouse Model: Phenotype Characterization and Gene TherapyPei-Hsuan Lin, Eugene Yu-Chuan Kang, Neoklis Makrides, et al.
Retina (Philadelphia, Pa.)|August 9, 2024
ADMINISTERING INTRAVITREAL BEVACIZUMAB FOR RETINOPATHY OF PREMATURITY: 8-Year Cognitive Outcomes In A Prospective CohortPei-Liang Wu, Chia-Pang Shih, Yu-Shu Huang, et al.
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