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Rebecca Procopio

Showing results (1-10 of 14) with videos related to

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Retinal Cases & Brief Reports|October 14, 2024
Secondary Multiple Evanescent White Dot Syndrome in a patient with North Carolina Macular DystrophyNikhil Bommakanti, Rebecca Procopio, Jose S Pulido
International Journal of Molecular Sciences|January 21, 2023
Initial Investigations of Intrinsically Disordered Regions in Inherited Retinal DiseasesKaren E Lee, Rebecca Procopio, Jose S Pulido, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
International Journal of Retina and Vitreous|December 30, 2025
Concentric macular rings and OCT corrugations in foveal hypoplasia: proof of concept for an optical interference mechanismAri H August, Ralph C Eagle, Tatyana Milman, et al.
Genes|August 26, 2023
A Comprehensive Report of Intrinsically Disordered Regions in Inherited Retinal DiseasesKaren E Lee, Jose S Pulido, Mariana M da Palma, et al.
American Journal of Ophthalmology Case Reports|February 7, 2025
Superotemporal predisposition to traumatic subretinal fibrosis in Stargardt disease: A case reportJamie A Nassur, Jose S Pulido, Rebecca Procopio, et al.
Ophthalmic Genetics|April 16, 2026
Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathyRoselind L Ni, Rebecca Procopio, Ezann Siebert, et al.
Cornea|September 15, 2023
Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea SyndromeBonnie A Sklar, Phattrawan Pisuchpen, Mor Bareket, et al.
Genes|March 29, 2023
Comparing Gene Panels for Non-Retinal Indications: A Systematic ReviewRebecca Procopio, Jose S Pulido, Kammi B Gunton, et al.
Ophthalmic Genetics|January 5, 2026
Novel variant in <i>FGFR2</i> in a family with anterior segment anomaliesGoura Chattannavar, Lorena M Haefeli, Rebecca Procopio, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Retinal Cases & Brief Reports|October 14, 2024
Secondary Multiple Evanescent White Dot Syndrome in a patient with North Carolina Macular DystrophyNikhil Bommakanti, Rebecca Procopio, Jose S Pulido
International Journal of Molecular Sciences|January 21, 2023
Initial Investigations of Intrinsically Disordered Regions in Inherited Retinal DiseasesKaren E Lee, Rebecca Procopio, Jose S Pulido, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
International Journal of Retina and Vitreous|December 30, 2025
Concentric macular rings and OCT corrugations in foveal hypoplasia: proof of concept for an optical interference mechanismAri H August, Ralph C Eagle, Tatyana Milman, et al.
Genes|August 26, 2023
A Comprehensive Report of Intrinsically Disordered Regions in Inherited Retinal DiseasesKaren E Lee, Jose S Pulido, Mariana M da Palma, et al.
American Journal of Ophthalmology Case Reports|February 7, 2025
Superotemporal predisposition to traumatic subretinal fibrosis in Stargardt disease: A case reportJamie A Nassur, Jose S Pulido, Rebecca Procopio, et al.
Ophthalmic Genetics|April 16, 2026
Gain of function in BEST1: photoreceptor changes and myopia in autosomal dominant vitreoretinochoroidopathyRoselind L Ni, Rebecca Procopio, Ezann Siebert, et al.
Cornea|September 15, 2023
Identification and Management of a Novel PRDM5 Gene Pathologic Variant in a Family With Brittle Cornea SyndromeBonnie A Sklar, Phattrawan Pisuchpen, Mor Bareket, et al.
Genes|March 29, 2023
Comparing Gene Panels for Non-Retinal Indications: A Systematic ReviewRebecca Procopio, Jose S Pulido, Kammi B Gunton, et al.
Ophthalmic Genetics|January 5, 2026
Novel variant in <i>FGFR2</i> in a family with anterior segment anomaliesGoura Chattannavar, Lorena M Haefeli, Rebecca Procopio, et al.
Pageof 2