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Anthony G Robson

Showing results (101-110 of 188) with videos related to

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Eye (London, England)|March 13, 2026
10-year experience in the use of Intravenous Immunoglobulin for Autoimmune RetinopathyAlan R Abraham, Lina Kobayter, Ester Carreno, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 22, 2026
ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli identificationJan Kremers, Mirella T S Barboni, Andrew J Zele, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, 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.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 26, 2026
Correction: ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuliJan Kremers, Mirella T S Barboni, Andrew J Zele, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 19

Showing results (101-110 of 188) with videos related to

Sort By:
Pageof 19
Eye (London, England)|March 13, 2026
10-year experience in the use of Intravenous Immunoglobulin for Autoimmune RetinopathyAlan R Abraham, Lina Kobayter, Ester Carreno, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 22, 2026
ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli identificationJan Kremers, Mirella T S Barboni, Andrew J Zele, et al.
American Journal of Ophthalmology|November 10, 2019
GUCY2D-Associated Leber Congenital Amaurosis: A Retrospective Natural History Study in Preparation for Trials of Novel TherapiesZaina Bouzia, Michalis Georgiou, Sarah Hull, 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.
Molecular Vision|December 4, 2009
A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunctionRobert H Henderson, Kathleen A Williamson, Joanna S Kennedy, et al.
American Journal of Human Genetics|November 3, 2009
Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humansZheng Li, Panagiotis I Sergouniotis, Michel Michaelides, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 26, 2026
Correction: ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuliJan Kremers, Mirella T S Barboni, Andrew J Zele, et al.
The British Journal of Ophthalmology|December 17, 2011
Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2Mala Subash, Tryfonas Rotsos, Genevieve A Wright, et al.
Investigative Ophthalmology & Visual Science|December 12, 2019
Deep Phenotyping of PDE6C-Associated AchromatopsiaMichalis Georgiou, Anthony G Robson, Navjit Singh, et al.
Pageof 19