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Alejandro J Roman

Showing results (51-60 of 96) with videos related to

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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.
Genes|July 15, 2017
EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease ProgressionDavid B McGuigan, Elise Heon, 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 <i>CEP2</i>90-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.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Experimental Eye Research|January 27, 2005
Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measuresAlejandro J Roman, Sharon B Schwartz, Tomas S Aleman, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
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.
Genes|July 15, 2017
EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease ProgressionDavid B McGuigan, Elise Heon, 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 <i>CEP2</i>90-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.
Proceedings of the National Academy of Sciences of the United States of America|January 24, 2013
Human retinal gene therapy for Leber congenital amaurosis shows advancing retinal degeneration despite enduring visual improvementArtur V Cideciyan, Samuel G Jacobson, William A Beltran, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Retinal laminar architecture in human retinitis pigmentosa caused by Rhodopsin gene mutationsTomas S Aleman, Artur V Cideciyan, Alexander Sumaroka, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
Experimental Eye Research|January 27, 2005
Quantifying rod photoreceptor-mediated vision in retinal degenerations: dark-adapted thresholds as outcome measuresAlejandro J Roman, Sharon B Schwartz, Tomas S Aleman, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Pageof 10