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Investigative Ophthalmology & Visual Science
|
October 27, 2022
Foveal Cone Structure in Patients With Blue Cone Monochromacy
Emily J Patterson, Angelos Kalitzeos, Thomas M Kane, et al.
Investigative Ophthalmology & Visual Science
|
January 26, 2019
Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability
Michalis Georgiou, Katie M Litts, Angelos Kalitzeos, et al.
Ophthalmic Genetics
|
May 4, 2026
<i>MERTK</i>-associated retinal dystrophy: clinical course and imaging
Thales A C de Guimarães, Juan Romo-Aguas, Nancy Aychoua, et al.
Investigative Ophthalmology & Visual Science
|
December 12, 2019
Deep Phenotyping of PDE6C-Associated Achromatopsia
Michalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science
|
April 30, 2020
Retinal Structure in RPE65-Associated Retinal Dystrophy
Neruban Kumaran, Michalis Georgiou, James W B Bainbridge, et al.
Ophthalmology
|
January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy
Kamron N Khan, Melissa Kasilian, Omar A R Mahroo, et al.
Investigative Ophthalmology & Visual Science
|
July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History
Thales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Translational Vision Science & Technology
|
August 21, 2020
Longitudinal Assessment of Remnant Foveal Cone Structure in a Case Series of Early Macular Telangiectasia Type 2
Katie M Litts, Mali Okada, Tjebo F C Heeren, et al.
Progress in Retinal and Eye Research
|
January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science
|
April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome
Juan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
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of 7
Search research articles
Search
Showing results (41-50 of 65) with videos related to
Sort By:
Page
of 7
Investigative Ophthalmology & Visual Science
|
October 27, 2022
Foveal Cone Structure in Patients With Blue Cone Monochromacy
Emily J Patterson, Angelos Kalitzeos, Thomas M Kane, et al.
Investigative Ophthalmology & Visual Science
|
January 26, 2019
Adaptive Optics Retinal Imaging in CNGA3-Associated Achromatopsia: Retinal Characterization, Interocular Symmetry, and Intrafamilial Variability
Michalis Georgiou, Katie M Litts, Angelos Kalitzeos, et al.
Ophthalmic Genetics
|
May 4, 2026
<i>MERTK</i>-associated retinal dystrophy: clinical course and imaging
Thales A C de Guimarães, Juan Romo-Aguas, Nancy Aychoua, et al.
Investigative Ophthalmology & Visual Science
|
December 12, 2019
Deep Phenotyping of PDE6C-Associated Achromatopsia
Michalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science
|
April 30, 2020
Retinal Structure in RPE65-Associated Retinal Dystrophy
Neruban Kumaran, Michalis Georgiou, James W B Bainbridge, et al.
Ophthalmology
|
January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy
Kamron N Khan, Melissa Kasilian, Omar A R Mahroo, et al.
Investigative Ophthalmology & Visual Science
|
July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural History
Thales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Translational Vision Science & Technology
|
August 21, 2020
Longitudinal Assessment of Remnant Foveal Cone Structure in a Case Series of Early Macular Telangiectasia Type 2
Katie M Litts, Mali Okada, Tjebo F C Heeren, et al.
Progress in Retinal and Eye Research
|
January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
Michalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Investigative Ophthalmology & Visual Science
|
April 21, 2025
Detailed Clinical, Ophthalmic, and Genetic Characterization of MYO7A-Associated Usher Syndrome
Juan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
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of 7