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Retina (Philadelphia, Pa.)|May 13, 2025
Bilateral Idiopathic Multifocal Pigment Epithelial Detachments: A Case Series and Review of LiteratureSamer Khateb, Sean Ghiam, Jordan Safran, et al.
Ophthalmology|January 25, 2015
Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene TherapyLina Zelinger, Artur V Cideciyan, Susanne Kohl, et al.
Investigative Ophthalmology & Visual Science|January 28, 2026
Enzymatic Disruption of the Internal Limiting Membrane Enhances Transplanted Retinal Ganglion Cell SurvivalDimitrios Stavropoulos, Chia-Chun Liu, Chi-Yu Chen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2022
Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamilyTalya Millo, Antonio Rivera, Alexey Obolensky, et al.
Investigative Ophthalmology & Visual Science|February 27, 2024
Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli PopulationAvigail Beryozkin, Ifat Sher, Miriam Ehrenberg, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 15, 2023
Coagulase-negative staphylococcal endophthalmitis: clinical severity and outcomes based on speciationJennifer O Adeghate, Sanya Yadav, Regis P Kowalski, et al.
NPJ Genomic Medicine|June 30, 2021
Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRDRiccardo Sangermano, Iris Deitch, Virginie G Peter, et al.
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