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Alejandro J Roman

Showing results (11-20 of 96) with videos related to

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Investigative Ophthalmology & Visual Science|June 17, 2016
Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone DiseasesArtur V Cideciyan, Alejandro J Roman, Samuel G Jacobson, et al.
The New England Journal of Medicine|May 5, 2015
Improvement and decline in vision with gene therapy in childhood blindnessSamuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|June 16, 2016
Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical TrialsDavid B McGuigan, Alejandro J Roman, Artur V Cideciyan, et al.
Translational Vision Science & Technology|December 21, 2020
Reading Performance in Blue Cone Monochromacy: Defining an Outcome Measure for a Clinical TrialEvelyn P Semenov, Rebecca Sheplock, Alejandro J Roman, et al.
Expert Opinion on Orphan Drugs|August 7, 2015
Improvement in vision: a new goal for treatment of hereditary retinal degenerationsSamuel G Jacobson, Artur V Cideciyan, Gustavo D Aguirre, et al.
Vision Research|February 24, 2020
Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone functionArun K Krishnan, Samuel G Jacobson, Alejandro J Roman, et al.
Ophthalmology|February 20, 2007
Leber congenital amaurosis caused by an RPGRIP1 mutation shows treatment potentialSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Frontiers in Cell and Developmental Biology|September 6, 2021
A Novel <i>ARL3</i> Gene Mutation Associated With Autosomal Dominant Retinal DegenerationRinki Ratnapriya, Samuel G Jacobson, Artur V Cideciyan, et al.
BMC Ophthalmology|June 14, 2022
Mobility test to assess functional vision in dark-adapted patients with Leber congenital amaurosisAlejandro J Roman, Artur V Cideciyan, Vivian Wu, et al.
Investigative Ophthalmology & Visual Science|April 14, 2017
Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D GeneGeoffrey K Aguirre, Omar H Butt, Ritobrato Datta, et al.
Pageof 10

Showing results (11-20 of 96) with videos related to

Sort By:
Pageof 10
Investigative Ophthalmology & Visual Science|June 17, 2016
Developing an Outcome Measure With High Luminance for Optogenetics Treatment of Severe Retinal Degenerations and for Gene Therapy of Cone DiseasesArtur V Cideciyan, Alejandro J Roman, Samuel G Jacobson, et al.
The New England Journal of Medicine|May 5, 2015
Improvement and decline in vision with gene therapy in childhood blindnessSamuel G Jacobson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|June 16, 2016
Automated Light- and Dark-Adapted Perimetry for Evaluating Retinitis Pigmentosa: Filling a Need to Accommodate Multicenter Clinical TrialsDavid B McGuigan, Alejandro J Roman, Artur V Cideciyan, et al.
Translational Vision Science & Technology|December 21, 2020
Reading Performance in Blue Cone Monochromacy: Defining an Outcome Measure for a Clinical TrialEvelyn P Semenov, Rebecca Sheplock, Alejandro J Roman, et al.
Expert Opinion on Orphan Drugs|August 7, 2015
Improvement in vision: a new goal for treatment of hereditary retinal degenerationsSamuel G Jacobson, Artur V Cideciyan, Gustavo D Aguirre, et al.
Vision Research|February 24, 2020
Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone functionArun K Krishnan, Samuel G Jacobson, Alejandro J Roman, et al.
Ophthalmology|February 20, 2007
Leber congenital amaurosis caused by an RPGRIP1 mutation shows treatment potentialSamuel G Jacobson, Artur V Cideciyan, Tomas S Aleman, et al.
Frontiers in Cell and Developmental Biology|September 6, 2021
A Novel <i>ARL3</i> Gene Mutation Associated With Autosomal Dominant Retinal DegenerationRinki Ratnapriya, Samuel G Jacobson, Artur V Cideciyan, et al.
BMC Ophthalmology|June 14, 2022
Mobility test to assess functional vision in dark-adapted patients with Leber congenital amaurosisAlejandro J Roman, Artur V Cideciyan, Vivian Wu, et al.
Investigative Ophthalmology & Visual Science|April 14, 2017
Postretinal Structure and Function in Severe Congenital Photoreceptor Blindness Caused by Mutations in the GUCY2D GeneGeoffrey K Aguirre, Omar H Butt, Ritobrato Datta, et al.
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