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Angelos Kalitzeos

Showing results (41-50 of 65) with videos related to

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Investigative Ophthalmology & Visual Science|October 27, 2022
Foveal Cone Structure in Patients With Blue Cone MonochromacyEmily 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 VariabilityMichalis Georgiou, Katie M Litts, Angelos Kalitzeos, et al.
Ophthalmic Genetics|May 4, 2026
<i>MERTK</i>-associated retinal dystrophy: clinical course and imagingThales A C de Guimarães, Juan Romo-Aguas, Nancy Aychoua, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science|April 30, 2020
Retinal Structure in RPE65-Associated Retinal DystrophyNeruban Kumaran, Michalis Georgiou, James W B Bainbridge, et al.
Ophthalmology|January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated RetinopathyKamron 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 HistoryThales 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 2Katie 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 syndromesMichalis 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 SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Investigative Ophthalmology & Visual Science|October 27, 2022
Foveal Cone Structure in Patients With Blue Cone MonochromacyEmily 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 VariabilityMichalis Georgiou, Katie M Litts, Angelos Kalitzeos, et al.
Ophthalmic Genetics|May 4, 2026
<i>MERTK</i>-associated retinal dystrophy: clinical course and imagingThales A C de Guimarães, Juan Romo-Aguas, Nancy Aychoua, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Investigative Ophthalmology & Visual Science|April 30, 2020
Retinal Structure in RPE65-Associated Retinal DystrophyNeruban Kumaran, Michalis Georgiou, James W B Bainbridge, et al.
Ophthalmology|January 10, 2018
Early Patterns of Macular Degeneration in ABCA4-Associated RetinopathyKamron 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 HistoryThales 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 2Katie 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 syndromesMichalis 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 SyndromeJuan C Romo-Aguas, Thales A C de Guimarães, Angelos Kalitzeos, et al.
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