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Investigative Ophthalmology & Visual Science|December 28, 2013
Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod functionAndrew Stockman, G Bruce Henning, Michel Michaelides, et al.Journal of Vision|March 6, 2008
The loss of the PDE6 deactivating enzyme, RGS9, results in precocious light adaptation at low light levelsAndrew Stockman, Hannah E Smithson, Andrew R Webster, et al.Investigative Ophthalmology & Visual Science|January 16, 2014
Vision in observers with enhanced S-cone syndrome: an excess of s-cones but connected mainly to conventional s-cone pathwaysCaterina Ripamonti, Jonathan Aboshiha, G Bruce Henning, et al.Journal of Vision|November 26, 2015
Spectral sensitivity measurements reveal partial success in restoring missing rod function with gene therapyCaterina Ripamonti, G Bruce Henning, Scott J Robbie, et al.Investigative Ophthalmology & Visual Science|September 27, 2014
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65Caterina Ripamonti, G Bruce Henning, Robin R Ali, et al.Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.American Journal of Human Genetics|June 29, 2010
X-linked cone dystrophy caused by mutation of the red and green cone opsinsJessica C Gardner, Tom R Webb, Naheed Kanuga, et al.The New England Journal of Medicine|April 29, 2008
Effect of gene therapy on visual function in Leber's congenital amaurosisJames W B Bainbridge, Alexander J Smith, Susie S Barker, et al.American Journal of Ophthalmology|April 26, 2022
WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease ProgressionAnna Majander, Neringa Jurkute, Florence Burté, et al.Pageof 6