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Ophthalmic Genetics|January 19, 2021
Variable expressivity in patients with autosomal recessive retinitis pigmentosa associated with the gene CNGB1Bojana Radojevic, Kaylie Jones, Martin Klein, et al.
Investigative Ophthalmology & Visual Science|April 26, 2014
Examination of VLC-PUFA-deficient photoreceptor terminalsLea D Bennett, Blake R Hopiavuori, Richard S Brush, et al.
Genes|January 21, 2023
Genetic Diagnosis for 64 Patients with Inherited Retinal DiseaseJacob Lynn, Austin Raney, Nathaniel Britton, et al.
Investigative Ophthalmology & Visual Science|April 12, 2014
Effect of reduced retinal VLC-PUFA on rod and cone photoreceptorsLea D Bennett, Richard S Brush, Michael Chan, et al.
American Journal of Ophthalmology|October 6, 2025
Development and Validation of a Commercially Available Two Color Dark Adapted Perimetry to Assess Inherited Retinal DegenerationsMark E Pennesi, Alessia Amato, Wayne Tschetter, et al.
Investigative Ophthalmology & Visual Science|July 21, 2022
Delineating the Clinical Phenotype of Patients With the c.629C>G, p.Pro210Arg Mutation in Peripherin-2Shannon M Conley, Cynthia K McClard, Maggie L Mwoyosvi, et al.
Investigative Ophthalmology & Visual Science|December 15, 2018
Prospective Evaluation of Patients With X-Linked Retinoschisis During 18 MonthsMark E Pennesi, David G Birch, K Thiran Jayasundera, et al.
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