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Edwin M Stone

Showing results (51-60 of 384) with videos related to

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Veterinary Ophthalmology|May 27, 2010
Effects of hereditary retinal degeneration due to a CEP290 mutation on the feline pupillary light reflexStewart Thompson, Rebecca E H Whiting, Randy H Kardon, et al.
American Journal of Ophthalmology|July 3, 2007
Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 geneByron L Lam, Jeffrey L Goldberg, Kristen L Hartley, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosisRichard G Weleber, Michel Michaelides, Karmen M Trzupek, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 16, 2010
Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the probandPhoebe Lin, Suma P Shankar, Jacque Duncan, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Computational quantification of complex fundus phenotypes in age-related macular degeneration and Stargardt diseaseGwenole Quellec, Stephen R Russell, Todd E Scheetz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2011
Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complicationsAlessandro Iannaccone, Natalie C Kerr, Tyson R Kinnick, et al.
Investigative Ophthalmology & Visual Science|September 18, 2015
Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease FrontArtur V Cideciyan, Malgorzata Swider, Sharon B Schwartz, et al.
Science Translational Medicine|June 12, 2015
Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesisTheodore G Drivas, Adam P Wojno, Budd A Tucker, et al.
Retina (Philadelphia, Pa.)|March 17, 2023
MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATIONAaron M Ricca, Ian C Han, Jeremy Hoffmann, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Complement component C5a activates ICAM-1 expression on human choroidal endothelial cellsJessica M Skeie, John H Fingert, Stephen R Russell, et al.
Pageof 39

Showing results (51-60 of 384) with videos related to

Sort By:
Pageof 39
Veterinary Ophthalmology|May 27, 2010
Effects of hereditary retinal degeneration due to a CEP290 mutation on the feline pupillary light reflexStewart Thompson, Rebecca E H Whiting, Randy H Kardon, et al.
American Journal of Ophthalmology|July 3, 2007
Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 geneByron L Lam, Jeffrey L Goldberg, Kristen L Hartley, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
The phenotype of Severe Early Childhood Onset Retinal Dystrophy (SECORD) from mutation of RPE65 and differentiation from Leber congenital amaurosisRichard G Weleber, Michel Michaelides, Karmen M Trzupek, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|March 16, 2010
Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the probandPhoebe Lin, Suma P Shankar, Jacque Duncan, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Computational quantification of complex fundus phenotypes in age-related macular degeneration and Stargardt diseaseGwenole Quellec, Stephen R Russell, Todd E Scheetz, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 16, 2011
Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complicationsAlessandro Iannaccone, Natalie C Kerr, Tyson R Kinnick, et al.
Investigative Ophthalmology & Visual Science|September 18, 2015
Predicting Progression of ABCA4-Associated Retinal Degenerations Based on Longitudinal Measurements of the Leading Disease FrontArtur V Cideciyan, Malgorzata Swider, Sharon B Schwartz, et al.
Science Translational Medicine|June 12, 2015
Basal exon skipping and genetic pleiotropy: A predictive model of disease pathogenesisTheodore G Drivas, Adam P Wojno, Budd A Tucker, et al.
Retina (Philadelphia, Pa.)|March 17, 2023
MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATIONAaron M Ricca, Ian C Han, Jeremy Hoffmann, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Complement component C5a activates ICAM-1 expression on human choroidal endothelial cellsJessica M Skeie, John H Fingert, Stephen R Russell, et al.
Pageof 39