Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
Retinal Cases & Brief Reports
|
October 14, 2024
Secondary Multiple Evanescent White Dot Syndrome in a patient with North Carolina Macular Dystrophy
Nikhil Bommakanti, Rebecca Procopio, Jose S Pulido
International Journal of Molecular Sciences
|
January 21, 2023
Initial Investigations of Intrinsically Disordered Regions in Inherited Retinal Diseases
Karen E Lee, Rebecca Procopio, Jose S Pulido, et al.
Ophthalmic Genetics
|
December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosa
Diego 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 mechanism
Ari H August, Ralph C Eagle, Tatyana Milman, et al.
Genes
|
August 26, 2023
A Comprehensive Report of Intrinsically Disordered Regions in Inherited Retinal Diseases
Karen 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 report
Jamie 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 vitreoretinochoroidopathy
Roselind 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 Syndrome
Bonnie A Sklar, Phattrawan Pisuchpen, Mor Bareket, et al.
Genes
|
March 29, 2023
Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
Rebecca 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 anomalies
Goura Chattannavar, Lorena M Haefeli, Rebecca Procopio, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Retinal Cases & Brief Reports
|
October 14, 2024
Secondary Multiple Evanescent White Dot Syndrome in a patient with North Carolina Macular Dystrophy
Nikhil Bommakanti, Rebecca Procopio, Jose S Pulido
International Journal of Molecular Sciences
|
January 21, 2023
Initial Investigations of Intrinsically Disordered Regions in Inherited Retinal Diseases
Karen E Lee, Rebecca Procopio, Jose S Pulido, et al.
Ophthalmic Genetics
|
December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosa
Diego 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 mechanism
Ari H August, Ralph C Eagle, Tatyana Milman, et al.
Genes
|
August 26, 2023
A Comprehensive Report of Intrinsically Disordered Regions in Inherited Retinal Diseases
Karen 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 report
Jamie 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 vitreoretinochoroidopathy
Roselind 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 Syndrome
Bonnie A Sklar, Phattrawan Pisuchpen, Mor Bareket, et al.
Genes
|
March 29, 2023
Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
Rebecca 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 anomalies
Goura Chattannavar, Lorena M Haefeli, Rebecca Procopio, et al.
Page
of 2