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Andrew R Webster

Showing results (211-220 of 372) with videos related to

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Investigative Ophthalmology & Visual Science|December 7, 2007
An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophyRobert H Henderson, Naushin Waseem, Rowan Searle, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
Investigative Ophthalmology & Visual Science|October 4, 2014
Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone healthAdam M Dubis, Robert F Cooper, Jonathan Aboshiha, et al.
Translational Vision Science & Technology|September 30, 2022
Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field ElectroretinographySophie L Glinton, Antonio Calcagni, Watjana Lilaonitkul, et al.
JAMA Ophthalmology|November 26, 2025
Clinical Findings and Molecular Genetics of USH1C-Associated Usher SyndromeNancy Aychoua, Thales A C de Guimarães, Manav B Ponnekanti, et al.
Ophthalmology|November 24, 2022
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural HistoryMichalis Georgiou, Anthony G Robson, Katarina Jovanovic, et al.
Translational Vision Science & Technology|August 22, 2020
Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular DegenerationKamron N Khan, Shyamanga Borooah, Leonardo Lando, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2022
Electrical responses from human retinal cone pathways associate with a common genetic polymorphism implicated in myopiaXiaofan Jiang, Zihe Xu, Talha Soorma, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Pageof 38

Showing results (211-220 of 372) with videos related to

Sort By:
Pageof 38
Investigative Ophthalmology & Visual Science|December 7, 2007
An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophyRobert H Henderson, Naushin Waseem, Rowan Searle, et al.
Investigative Ophthalmology & Visual Science|October 2, 2014
The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotypeSarah Hull, Gavin Arno, Vincent Plagnol, et al.
Investigative Ophthalmology & Visual Science|October 4, 2014
Genotype-dependent variability in residual cone structure in achromatopsia: toward developing metrics for assessing cone healthAdam M Dubis, Robert F Cooper, Jonathan Aboshiha, et al.
Translational Vision Science & Technology|September 30, 2022
Phenotyping of ABCA4 Retinopathy by Machine Learning Analysis of Full-Field ElectroretinographySophie L Glinton, Antonio Calcagni, Watjana Lilaonitkul, et al.
JAMA Ophthalmology|November 26, 2025
Clinical Findings and Molecular Genetics of USH1C-Associated Usher SyndromeNancy Aychoua, Thales A C de Guimarães, Manav B Ponnekanti, et al.
Ophthalmology|November 24, 2022
RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural HistoryMichalis Georgiou, Anthony G Robson, Katarina Jovanovic, et al.
Translational Vision Science & Technology|August 22, 2020
Quantifying the Separation Between the Retinal Pigment Epithelium and Bruch's Membrane using Optical Coherence Tomography in Patients with Inherited Macular DegenerationKamron N Khan, Shyamanga Borooah, Leonardo Lando, et al.
JAMA Ophthalmology|January 6, 2017
Clinical Characterization of CNGB1-Related Autosomal Recessive Retinitis PigmentosaSarah Hull, Marcella Attanasio, Gavin Arno, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2022
Electrical responses from human retinal cone pathways associate with a common genetic polymorphism implicated in myopiaXiaofan Jiang, Zihe Xu, Talha Soorma, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Pageof 38