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Investigative Ophthalmology & Visual Science|December 13, 2022
Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 MutationsArtur V Cideciyan, Samuel G Jacobson, Malgorzata Swider, et al.
Human Molecular Genetics|April 18, 2003
Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal laminationSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|October 3, 2009
Normal central retinal function and structure preserved in retinitis pigmentosaSamuel G Jacobson, Alejandro J Roman, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|January 2, 2007
RDH12 and RPE65, visual cycle genes causing leber congenital amaurosis, differ in disease expressionSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Investigative Ophthalmology & Visual Science|September 28, 2007
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|July 31, 2014
TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular conesSamuel G Jacobson, Artur V Cideciyan, Wei Chieh Huang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 13, 2019
Long-Term Structural Outcomes of Late-Stage RPE65 Gene TherapyKristin L Gardiner, Artur V Cideciyan, Malgorzata Swider, et al.
Translational Vision Science & Technology|January 24, 2023
Color Vision in Blue Cone Monochromacy: Outcome Measures for a Clinical TrialAbraham A Mascio, Alejandro J Roman, Artur V Cideciyan, et al.
American Journal of Ophthalmology Case Reports|June 30, 2023
Durable vision improvement after a single intravitreal treatment with antisense oligonucleotide in CEP290-LCA: Replication in two eyesArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Human Molecular Genetics|July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degenerationSamuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
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