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Alejandro J Roman

Showing results (31-40 of 96) with videos related to

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Scientific Reports|July 30, 2020
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutationsArtur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|December 25, 2014
Pseudo-fovea formation after gene therapy for RPE65-LCAArtur V Cideciyan, Geoffrey K Aguirre, Samuel G Jacobson, et al.
International Journal of Molecular Sciences|January 23, 2024
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an <i>ALG6</i> Modifier VariantElisha Monson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 6, 2018
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion MutationsAlexander Sumaroka, Alexandra V Garafalo, Artur V Cideciyan, et al.
Nature Medicine|April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case reportArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
International Journal of Molecular Sciences|May 24, 2019
Short-Wavelength Sensitive Cone (S-cone) Testing as an Outcome Measure for <i>NR2E3</i> Clinical Treatment TrialsAlejandro J Roman, Christian A Powers, Evelyn P Semenov, et al.
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Pageof 10

Showing results (31-40 of 96) with videos related to

Sort By:
Pageof 10
Scientific Reports|July 30, 2020
Rod function deficit in retained photoreceptors of patients with class B Rhodopsin mutationsArtur V Cideciyan, Samuel G Jacobson, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|December 25, 2014
Pseudo-fovea formation after gene therapy for RPE65-LCAArtur V Cideciyan, Geoffrey K Aguirre, Samuel G Jacobson, et al.
International Journal of Molecular Sciences|January 23, 2024
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an <i>ALG6</i> Modifier VariantElisha Monson, Artur V Cideciyan, Alejandro J Roman, et al.
Investigative Ophthalmology & Visual Science|May 21, 2010
Retinal disease in Rpe65-deficient mice: comparison to human leber congenital amaurosis due to RPE65 mutationsRafael C Caruso, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|January 2, 2009
Defining the residual vision in leber congenital amaurosis caused by RPE65 mutationsSamuel G Jacobson, Tomas S Aleman, Artur V Cideciyan, et al.
Investigative Ophthalmology & Visual Science|December 6, 2018
Blue Cone Monochromacy Caused by the C203R Missense Mutation or Large Deletion MutationsAlexander Sumaroka, Alexandra V Garafalo, Artur V Cideciyan, et al.
Nature Medicine|April 2, 2021
Durable vision improvement after a single treatment with antisense oligonucleotide sepofarsen: a case reportArtur V Cideciyan, Samuel G Jacobson, Allen C Ho, et al.
Investigative Ophthalmology & Visual Science|August 29, 2006
Remodeling of the human retina in choroideremia: rab escort protein 1 (REP-1) mutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
International Journal of Molecular Sciences|May 24, 2019
Short-Wavelength Sensitive Cone (S-cone) Testing as an Outcome Measure for <i>NR2E3</i> Clinical Treatment TrialsAlejandro J Roman, Christian A Powers, Evelyn P Semenov, et al.
Molecular Vision|October 26, 2007
Electroretinographic analyses of Rpe65-mutant rd12 mice: developing an in vivo bioassay for human gene therapy trials of Leber congenital amaurosisAlejandro J Roman, Sanford L Boye, Tomas S Aleman, et al.
Pageof 10