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Investigative Ophthalmology & Visual Science|August 30, 2011
Retinal disease course in Usher syndrome 1B due to MYO7A mutationsSamuel G Jacobson, Artur V Cideciyan, Dan Gibbs, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 12, 2011
Variations in NPHP5 in patients with nonsyndromic leber congenital amaurosis and Senior-Loken syndromeEdwin M Stone, Artur V Cideciyan, Tomas S Aleman, et al.
Human Molecular Genetics|August 11, 2016
Overlap of abnormal photoreceptor development and progressive degeneration in Leber congenital amaurosis caused by NPHP5 mutationLouise M Downs, Erin M Scott, Artur V Cideciyan, et al.
Human Mutation|October 2, 2004
Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone SyndromeAlan F Wright, Adam C Reddick, Sharon B Schwartz, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Macular pigment and lutein supplementation in ABCA4-associated retinal degenerationsTomas S Aleman, Artur V Cideciyan, Elizabeth A M Windsor, et al.
Investigative Ophthalmology & Visual Science|May 1, 2001
An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 22, 2018
Mutation-independent rhodopsin gene therapy by knockdown and replacement with a single AAV vectorArtur V Cideciyan, Raghavi Sudharsan, Valérie L Dufour, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 18, 1999
Stable transgene expression in rod photoreceptors after recombinant adeno-associated virus-mediated gene transfer to monkey retinaJ Bennett, A M Maguire, A V Cideciyan, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 14, 2015
Successful arrest of photoreceptor and vision loss expands the therapeutic window of retinal gene therapy to later stages of diseaseWilliam A Beltran, Artur V Cideciyan, Simone Iwabe, et al.
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