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Molecular Vision|December 24, 2011
A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a familyAjoy Vincent, Tom Wright, Megan A Day, et al.Ophthalmic Genetics|December 8, 2024
Highly asymmetric early presentation of FEVR requiring enucleationKirill Zaslavsky, Ajoy Vincent, Birgit Betina Ertl-Wagner, et al.Molecular Genetics & Genomic Medicine|April 11, 2018
ERCC6L2-associated inherited bone marrow failure syndromeIren Shabanova, Elisa Cohen, Michaela Cada, et al.Documenta Ophthalmologica. Advances in Ophthalmology|June 23, 2020
Rod bipolar cell dysfunction in POLG retinopathyKit Green Sanderson, Eoghan Millar, Anupreet Tumber, et al.Documenta Ophthalmologica. Advances in Ophthalmology|November 14, 2019
Unique retinal signaling defect in GNB5-related diseaseZhuo Shao, Anupreet Tumber, Jason Maynes, et al.Documenta Ophthalmologica. Advances in Ophthalmology|March 26, 2010
Functional involvement of cone photoreceptors in advanced glaucoma: a multifocal electroretinogram studyAjoy Vincent, Rohit Shetty, Sathi A V Devi, et al.Retina (Philadelphia, Pa.)|January 27, 2012
The characterization of retinal phenotype in a family with C1QTNF5-related late-onset retinal degenerationAjoy Vincent, Francis L Munier, Cynthia C Vandenhoven, et al.Investigative Ophthalmology & Visual Science|December 11, 2012
Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram"Ajoy Vincent, Tom Wright, Yaiza Garcia-Sanchez, et al.Genes|April 28, 2023
Retinal Phenotyping of a Murine Model of Lafora DiseaseAjoy Vincent, Kashif Ahmed, Rowaida Hussein, et al.Documenta Ophthalmologica. Advances in Ophthalmology|October 26, 2007
Electrophysiological and structural assessment of the central retina following intravitreal injection of bevacizumab for treatment of macular edemaRohit Shetty, Sivakami A Pai, Ajoy Vincent, et al.Pageof 9