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Isabelle Audo

Showing results (111-120 of 234) with videos related to

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Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Ophthalmology Science|March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene NeparvovecM Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Investigative Ophthalmology & Visual Science|March 24, 2017
LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar CellsMarion Neuillé, Yan Cao, Romain Caplette, et al.
American Journal of Ophthalmology|December 20, 2025
Autosomal Recessive Bestrophinopathy - Phenotypic variability, Natural History, and Genotype-phenotype correlationsLorenzo Bianco, Alessio Antropoli, Elise Boulanger-Scemama, et al.
Human Gene Therapy|July 6, 2024
An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI StudyRobert E MacLaren, Isabelle Audo, M Dominik Fischer, et al.
Ophthalmology and Therapy|February 27, 2023
Psychometric Validation of the ViSIO-PRO and ViSIO-ObsRO in Retinitis Pigmentosa and Leber Congenital AmaurosisM Dominik Fischer, Francesco Patalano, Christel Naujoks, et al.
Human Mutation|March 25, 2010
EYS is a major gene for rod-cone dystrophies in FranceIsabelle Audo, José-Alain Sahel, Saddek Mohand-Saïd, et al.
International Journal of Molecular Sciences|July 9, 2022
Retrospective Natural History Study of <i>RPGR</i>-Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the DiseaseMarco Nassisi, Giuseppe De Bartolo, Saddek Mohand-Said, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
Brain Communications|June 25, 2026
Magnetoencephalography biomarkers for assessing myelin content and neuronal function in acute optic neuritisYsoline Beigneux, Christophe Gitton, Abdul Rauf Anwar, et al.
Pageof 24

Showing results (111-120 of 234) with videos related to

Sort By:
Pageof 24
Human Mutation|April 17, 2018
MERTK mutation update in inherited retinal diseasesIsabelle Audo, Saddek Mohand-Said, Elise Boulanger-Scemama, et al.
Ophthalmology Science|March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene NeparvovecM Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Investigative Ophthalmology & Visual Science|March 24, 2017
LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar CellsMarion Neuillé, Yan Cao, Romain Caplette, et al.
American Journal of Ophthalmology|December 20, 2025
Autosomal Recessive Bestrophinopathy - Phenotypic variability, Natural History, and Genotype-phenotype correlationsLorenzo Bianco, Alessio Antropoli, Elise Boulanger-Scemama, et al.
Human Gene Therapy|July 6, 2024
An Open-Label Phase II Study Assessing the Safety of Bilateral, Sequential Administration of Retinal Gene Therapy in Participants with Choroideremia: The GEMINI StudyRobert E MacLaren, Isabelle Audo, M Dominik Fischer, et al.
Ophthalmology and Therapy|February 27, 2023
Psychometric Validation of the ViSIO-PRO and ViSIO-ObsRO in Retinitis Pigmentosa and Leber Congenital AmaurosisM Dominik Fischer, Francesco Patalano, Christel Naujoks, et al.
Human Mutation|March 25, 2010
EYS is a major gene for rod-cone dystrophies in FranceIsabelle Audo, José-Alain Sahel, Saddek Mohand-Saïd, et al.
International Journal of Molecular Sciences|July 9, 2022
Retrospective Natural History Study of <i>RPGR</i>-Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the DiseaseMarco Nassisi, Giuseppe De Bartolo, Saddek Mohand-Said, et al.
Biomed Research International|February 19, 2015
Targeted next generation sequencing identifies novel mutations in RP1 as a relatively common cause of autosomal recessive rod-cone dystrophySaid El Shamieh, Elise Boulanger-Scemama, Marie-Elise Lancelot, et al.
Brain Communications|June 25, 2026
Magnetoencephalography biomarkers for assessing myelin content and neuronal function in acute optic neuritisYsoline Beigneux, Christophe Gitton, Abdul Rauf Anwar, et al.
Pageof 24