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Eye (London, England)|August 16, 2008
Genetic heterogeneity in autosomal dominant retinitis pigmentosa with low-frequency damped electroretinographic waveletsT S Aleman, B L Lam, A V Cideciyan, et al.Ophthalmology|November 30, 2000
Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degenerationA H Milam, C A Curcio, A V Cideciyan, et al.American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.Investigative Ophthalmology & Visual Science|June 30, 2001
Macular pigment and lutein supplementation in retinitis pigmentosa and Usher syndromeT S Aleman, J L Duncan, M L Bieber, et al.Documenta Ophthalmologica. Advances in Ophthalmology|January 18, 2024
ISCEV and IPS guideline for the full-field stimulus test (FST)J K Jolly, J R Grigg, A M McKendrick, et al.Investigative Ophthalmology & Visual Science|August 10, 1999
Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degenerationC A Lewis, I R Batlle, K G Batlle, et al.Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.Nature Genetics|April 28, 2001
Gene therapy restores vision in a canine model of childhood blindnessG M Acland, G D Aguirre, J Ray, et al.Nature Biotechnology|October 23, 1997
Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosaR M Petters, C A Alexander, K D Wells, et al.Pageof 5