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Anthony G Robson

Showing results (51-60 of 188) with videos related to

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Documenta Ophthalmologica. Advances in Ophthalmology|June 24, 2018
ISCEV extended protocol for the photopic On-Off ERGMaja Sustar, Graham E Holder, Jan Kremers, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 1, 2019
ISCEV extended protocol for the stimulus-response series for light-adapted full-field ERGDaphne L McCulloch, Mineo Kondo, Ruth Hamilton, et al.
The British Journal of Ophthalmology|February 25, 2016
Preserved visual function in retinal dystrophy due to hypomorphic <i>RPE65</i> mutationsSarah Hull, Graham E Holder, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 25, 2021
ISCEV standard for clinical multifocal electroretinography (mfERG) (2021 update)Michael B Hoffmann, Michael Bach, Mineo Kondo, et al.
Orphanet Journal of Rare Diseases|March 13, 2021
Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophyMichalis Georgiou, Naser Ali, Elizabeth Yang, et al.
Retina (Philadelphia, Pa.)|March 11, 2014
Prph2 mutations as a cause of electronegative ERGRola Ba-Abbad, Anthony G Robson, Yew C Yap, et al.
Investigative Ophthalmology & Visual Science|October 27, 2004
Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Catherine A Egan, Vy A Luong, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 5, 2011
Electroretinogram measures in a septuagenarian populationMagella M Neveu, Alan Dangour, Elizabeth Allen, et al.
Ophthalmology. Retina|July 18, 2020
Enhanced S-Cone Syndrome: Spectrum of Clinical, Imaging, Electrophysiologic, and Genetic Findings in a Retrospective Case Series of 56 PatientsEmanuel R de Carvalho, Anthony G Robson, Gavin Arno, et al.
American Journal of Ophthalmology Case Reports|April 13, 2019
Isolated rod dysfunction associated with a novel genotype of <i>CNGB1</i>Rola Ba-Abbad, Graham E Holder, Anthony G Robson, et al.
Pageof 19

Showing results (51-60 of 188) with videos related to

Sort By:
Pageof 19
Documenta Ophthalmologica. Advances in Ophthalmology|June 24, 2018
ISCEV extended protocol for the photopic On-Off ERGMaja Sustar, Graham E Holder, Jan Kremers, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|April 1, 2019
ISCEV extended protocol for the stimulus-response series for light-adapted full-field ERGDaphne L McCulloch, Mineo Kondo, Ruth Hamilton, et al.
The British Journal of Ophthalmology|February 25, 2016
Preserved visual function in retinal dystrophy due to hypomorphic <i>RPE65</i> mutationsSarah Hull, Graham E Holder, Anthony G Robson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|January 25, 2021
ISCEV standard for clinical multifocal electroretinography (mfERG) (2021 update)Michael B Hoffmann, Michael Bach, Mineo Kondo, et al.
Orphanet Journal of Rare Diseases|March 13, 2021
Extending the phenotypic spectrum of PRPF8, PRPH2, RP1 and RPGR, and the genotypic spectrum of early-onset severe retinal dystrophyMichalis Georgiou, Naser Ali, Elizabeth Yang, et al.
Retina (Philadelphia, Pa.)|March 11, 2014
Prph2 mutations as a cause of electronegative ERGRola Ba-Abbad, Anthony G Robson, Yew C Yap, et al.
Investigative Ophthalmology & Visual Science|October 27, 2004
Comparison of fundus autofluorescence with photopic and scotopic fine-matrix mapping in patients with retinitis pigmentosa and normal visual acuityAnthony G Robson, Catherine A Egan, Vy A Luong, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|August 5, 2011
Electroretinogram measures in a septuagenarian populationMagella M Neveu, Alan Dangour, Elizabeth Allen, et al.
Ophthalmology. Retina|July 18, 2020
Enhanced S-Cone Syndrome: Spectrum of Clinical, Imaging, Electrophysiologic, and Genetic Findings in a Retrospective Case Series of 56 PatientsEmanuel R de Carvalho, Anthony G Robson, Gavin Arno, et al.
American Journal of Ophthalmology Case Reports|April 13, 2019
Isolated rod dysfunction associated with a novel genotype of <i>CNGB1</i>Rola Ba-Abbad, Graham E Holder, Anthony G Robson, et al.
Pageof 19