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Robert K Koenekoop

Showing results (1-10 of 122) with videos related to

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Ophthalmic Genetics|June 6, 2003
The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-reviewRobert K Koenekoop
Ophthalmic Genetics|January 28, 2011
Why some photoreceptors die, while others remain dormant: lessons from RPE65 and LRAT associated retinal dystrophiesRobert K Koenekoop
Ophthalmic Genetics|December 15, 2005
RPGRIP1 is mutated in Leber congenital amaurosis: a mini-reviewRobert K Koenekoop
Survey of Ophthalmology|July 3, 2004
An overview of Leber congenital amaurosis: a model to understand human retinal developmentRobert K Koenekoop
Ophthalmic Genetics|November 28, 2009
Why do cone photoreceptors die in rod-specific forms of retinal degenerations?Robert K Koenekoop
Ophthalmic Genetics|September 4, 2008
Successful RPE65 gene replacement and improved visual function in humansRobert K Koenekoop
Children (Basel, Switzerland)|October 29, 2025
Neural Network-Based Prediction of Post-Operative Visual Outcomes Following Secondary Pediatric Intraocular Lens ImplantationAndrew Farah, Raheem Remtulla, Robert K Koenekoop
Acta Ophthalmologica|December 9, 2022
Probing mechanisms and improving management of glaucoma following Boston keratoprosthesis surgeryDominique Geoffrion, Robert K Koenekoop, Mona Harissi-Dagher
Acta Ophthalmologica|February 16, 2023
Probing mechanisms and improving management of glaucoma following Boston keratoprosthesis surgeryDominique Geoffrion, Robert K Koenekoop, Mona Harissi-Dagher
Ophthalmic Genetics|January 18, 2017
Leber congenital amaurosis, from darkness to light: An ode to Irene MaumeneeRazek Georges Coussa, Irma Lopez Solache, Robert K Koenekoop
Pageof 13

Showing results (1-10 of 122) with videos related to

Sort By:
Pageof 13
Ophthalmic Genetics|June 6, 2003
The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-reviewRobert K Koenekoop
Ophthalmic Genetics|January 28, 2011
Why some photoreceptors die, while others remain dormant: lessons from RPE65 and LRAT associated retinal dystrophiesRobert K Koenekoop
Ophthalmic Genetics|December 15, 2005
RPGRIP1 is mutated in Leber congenital amaurosis: a mini-reviewRobert K Koenekoop
Survey of Ophthalmology|July 3, 2004
An overview of Leber congenital amaurosis: a model to understand human retinal developmentRobert K Koenekoop
Ophthalmic Genetics|November 28, 2009
Why do cone photoreceptors die in rod-specific forms of retinal degenerations?Robert K Koenekoop
Ophthalmic Genetics|September 4, 2008
Successful RPE65 gene replacement and improved visual function in humansRobert K Koenekoop
Children (Basel, Switzerland)|October 29, 2025
Neural Network-Based Prediction of Post-Operative Visual Outcomes Following Secondary Pediatric Intraocular Lens ImplantationAndrew Farah, Raheem Remtulla, Robert K Koenekoop
Acta Ophthalmologica|December 9, 2022
Probing mechanisms and improving management of glaucoma following Boston keratoprosthesis surgeryDominique Geoffrion, Robert K Koenekoop, Mona Harissi-Dagher
Acta Ophthalmologica|February 16, 2023
Probing mechanisms and improving management of glaucoma following Boston keratoprosthesis surgeryDominique Geoffrion, Robert K Koenekoop, Mona Harissi-Dagher
Ophthalmic Genetics|January 18, 2017
Leber congenital amaurosis, from darkness to light: An ode to Irene MaumeneeRazek Georges Coussa, Irma Lopez Solache, Robert K Koenekoop
Pageof 13