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Andrew R Webster

Showing results (191-200 of 372) with videos related to

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Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Ophthalmology. Retina|September 1, 2024
PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural HistoryShaima Awadh Hashem, Michalis Georgiou, Genevieve Wright, et al.
Plos One|March 30, 2017
Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt diseaseStanley Lambertus, Nathalie M Bax, Ana Fakin, 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.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
American Journal of Ophthalmology|February 16, 2024
Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal DystrophyShaima Awadh Hashem, Michalis Georgiou, Yu Fujinami-Yokokawa, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, 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.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Human Mutation|January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophyAlice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Pageof 38

Showing results (191-200 of 372) with videos related to

Sort By:
Pageof 38
Investigative Ophthalmology & Visual Science|June 6, 2025
Clinical and Biochemical Characterization of Specific GUCY2D Alleles Associated With a Rare Form of Night BlindnessRola Ba-Abbad, Igor V Peshenko, Malena Daich Varela, et al.
Ophthalmology. Retina|September 1, 2024
PDE6A-Associated Retinitis Pigmentosa, Clinical Characteristics, Genetics, and Natural HistoryShaima Awadh Hashem, Michalis Georgiou, Genevieve Wright, et al.
Plos One|March 30, 2017
Highly sensitive measurements of disease progression in rare disorders: Developing and validating a multimodal model of retinal degeneration in Stargardt diseaseStanley Lambertus, Nathalie M Bax, Ana Fakin, 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.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
American Journal of Ophthalmology|February 16, 2024
Genetics, Clinical Characteristics, and Natural History of PDE6B-Associated Retinal DystrophyShaima Awadh Hashem, Michalis Georgiou, Yu Fujinami-Yokokawa, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, 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.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Human Mutation|January 3, 2013
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophyAlice E Davidson, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Pageof 38