Showing results (41-50 of 110) with videos related to

Sort By:
Pageof 11
Investigative Ophthalmology & Visual Science|December 17, 2008
Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutationsSamuel G Jacobson, Tomas S Aleman, Alexander Sumaroka, et al.
Nature Medicine|April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case reportArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retinaArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 11, 2011
Defective photoreceptor phagocytosis in a mouse model of enhanced S-cone syndrome causes progressive retinal degenerationDebarshi Mustafi, Brian M Kevany, Christel Genoud, et al.
Investigative Ophthalmology & Visual Science|September 23, 2016
Complexity of the Class B Phenotype in Autosomal Dominant Retinitis Pigmentosa Due to Rhodopsin MutationsSamuel G Jacobson, David B McGuigan, Alexander Sumaroka, et al.
Ophthalmic Genetics|March 30, 2026
Bi-allelic pathogenic variants in NR2E3 may be associated with a subtle enhanced S-cone syndrome phenotypeAlexander Hüther, Caroline L Sherman, Alexander Sumaroka, et al.
American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Pageof 11