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Isabelle Audo

Showing results (161-170 of 234) with videos related to

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Investigative Ophthalmology & Visual Science|March 2, 2026
Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis PigmentosaEmmanuelle Clérin, Ying Yang, Delphine Pagan, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.
Current Eye Research|July 18, 2018
Usher Syndrome and Color VisionAnne Kurtenbach, Gesa Hahn, Christoph Kernstock, et al.
JAMA Ophthalmology|December 4, 2025
EGFLAM Pathogenic Variants and Congenital Stationary Night BlindnessSanja Boranijasevic, Vasily Smirnov, Julien Navarro, et al.
Translational Vision Science & Technology|October 13, 2016
Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy TrialMaria A Parker, Dongseok Choi, Laura R Erker, et al.
Investigative Ophthalmology & Visual Science|September 11, 2020
Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic FactorsVincent Lhussiez, Elisabeth Dubus, Quénol Cesar, et al.
Human Mutation|August 7, 2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsiaNicole Weisschuh, Katarina Stingl, Isabelle Audo, et al.
Ophthalmology Science|October 17, 2022
Retinitis Punctata Albescens and <i>RLBP1</i>-Allied Phenotypes: Phenotype-Genotype Correlation and Natural History in the Aim of Gene TherapyBéatrice Bocquet, Hicham El Alami Trebki, Anne Françoise Roux, et al.
Iscience|April 2, 2025
Reactivating the phototransduction cascade with a mutation agnostic gene therapy preserves vision in rod-cone dystrophiesCardillia-Joe Simon, Hanen Khabou, Antoine Chaffiol, et al.
American Journal of Ophthalmology|December 22, 2023
Functional Vision in Patients With Biallelic USH2A VariantsElise Heon, Michele Melia, Laura E Bocchino, et al.
Pageof 24

Showing results (161-170 of 234) with videos related to

Sort By:
Pageof 24
Investigative Ophthalmology & Visual Science|March 2, 2026
Combined Expression of hRdCVF and hRdCVFL Through AAV-Mediated Delivery for the Treatment of Retinitis PigmentosaEmmanuelle Clérin, Ying Yang, Delphine Pagan, et al.
Investigative Ophthalmology & Visual Science|May 26, 2005
Identification of novel RPGR ORF15 mutations in X-linked progressive cone-rod dystrophy (XLCORD) familiesNeil D Ebenezer, Michel Michaelides, Sharon A Jenkins, et al.
Current Eye Research|July 18, 2018
Usher Syndrome and Color VisionAnne Kurtenbach, Gesa Hahn, Christoph Kernstock, et al.
JAMA Ophthalmology|December 4, 2025
EGFLAM Pathogenic Variants and Congenital Stationary Night BlindnessSanja Boranijasevic, Vasily Smirnov, Julien Navarro, et al.
Translational Vision Science & Technology|October 13, 2016
Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy TrialMaria A Parker, Dongseok Choi, Laura R Erker, et al.
Investigative Ophthalmology & Visual Science|September 11, 2020
Cohen Syndrome-Associated Cataract Is Explained by VPS13B Functions in Lens Homeostasis and Is Modified by Additional Genetic FactorsVincent Lhussiez, Elisabeth Dubus, Quénol Cesar, et al.
Human Mutation|August 7, 2018
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsiaNicole Weisschuh, Katarina Stingl, Isabelle Audo, et al.
Ophthalmology Science|October 17, 2022
Retinitis Punctata Albescens and <i>RLBP1</i>-Allied Phenotypes: Phenotype-Genotype Correlation and Natural History in the Aim of Gene TherapyBéatrice Bocquet, Hicham El Alami Trebki, Anne Françoise Roux, et al.
Iscience|April 2, 2025
Reactivating the phototransduction cascade with a mutation agnostic gene therapy preserves vision in rod-cone dystrophiesCardillia-Joe Simon, Hanen Khabou, Antoine Chaffiol, et al.
American Journal of Ophthalmology|December 22, 2023
Functional Vision in Patients With Biallelic USH2A VariantsElise Heon, Michele Melia, Laura E Bocchino, et al.
Pageof 24