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Andrew R Webster

Showing results (171-180 of 372) with videos related to

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The British Journal of Ophthalmology|July 24, 2021
Foveal structure and visual function in nanophthalmos and posterior microphthalmosPhilipp L Müller, Tim Treis, Abdulrahman Alsaedi, et al.
Ophthalmology|January 26, 2024
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic FindingsYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Molecular Vision|January 5, 2011
A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1Alice E Davidson, Panagiotis I Sergouniotis, Rosemary Burgess-Mullan, et al.
Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
American Journal of Ophthalmology|October 8, 2023
IMPG2-Related MaculopathyJohannes Birtel, Richard Caswell, Samantha R De Silva, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, 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.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Pageof 38

Showing results (171-180 of 372) with videos related to

Sort By:
Pageof 38
The British Journal of Ophthalmology|July 24, 2021
Foveal structure and visual function in nanophthalmos and posterior microphthalmosPhilipp L Müller, Tim Treis, Abdulrahman Alsaedi, et al.
Ophthalmology|January 26, 2024
Best Vitelliform Macular Dystrophy Natural History Study Report 1: Clinical Features and Genetic FindingsYannik Laich, Michalis Georgiou, Kaoru Fujinami, et al.
Molecular Vision|January 5, 2011
A synonymous codon variant in two patients with autosomal recessive bestrophinopathy alters in vitro splicing of BEST1Alice E Davidson, Panagiotis I Sergouniotis, Rosemary Burgess-Mullan, et al.
Investigative Ophthalmology & Visual Science|March 11, 2026
Characterizing a Unique Retinal Phenotype in INTS11-Associated Neurodevelopmental DisorderSiying Lin, Wendy D Tan, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
American Journal of Ophthalmology|October 8, 2023
IMPG2-Related MaculopathyJohannes Birtel, Richard Caswell, Samantha R De Silva, et al.
Investigative Ophthalmology & Visual Science|November 23, 2013
A longitudinal study of Stargardt disease: quantitative assessment of fundus autofluorescence, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, 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.
Molecular Vision|April 3, 2010
A detailed phenotypic assessment of individuals affected by MFRP-related oculopathyRajarshi Mukhopadhyay, Panagiotis I Sergouniotis, Donna S Mackay, et al.
Pageof 38