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Anthony G Robson

Showing results (61-70 of 188) with videos related to

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Molecular Vision|November 23, 2013
Clinical characteristics of early retinal disease due to CDHR1 mutationRola Ba-Abbad, Panagiotis I Sergouniotis, Vincent Plagnol, et al.
Retina (Philadelphia, Pa.)|March 12, 2011
Serial imaging and structure-function correlates of high-density rings of fundus autofluorescence in retinitis pigmentosaAnthony G Robson, Adnan Tufail, Fred Fitzke, et al.
Acta Ophthalmologica|January 8, 2013
Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration)Vasileios Soumplis, Panagiotis I Sergouniotis, Anthony G Robson, et al.
Acta Ophthalmologica|October 20, 2011
A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 genePanagiotis I Sergouniotis, Anthony G Robson, Zheng Li, et al.
Ophthalmic Genetics|August 14, 2020
Macula-predominant retinopathy associated with biallelic variants in <i>RDH12</i>Rola Ba-Abbad, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 3, 2023
ISCEV guidelines for calibration and verification of stimuli and recording instruments (2023 update)Daphne L McCulloch, Michael Bach, Mitchell Brigell, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 5, 2022
ISCEV Standard for full-field clinical electroretinography (2022 update)Anthony G Robson, Laura J Frishman, John Grigg, et al.
Ophthalmology|March 5, 2013
A phenotype-genotype correlation study of X-linked retinoschisisAjoy Vincent, Anthony G Robson, Magella M Neveu, et al.
Investigative Ophthalmology & Visual Science|July 28, 2004
Fundus autofluorescence in patients with leber congenital amaurosisHendrik P N Scholl, N H Victor Chong, Anthony G Robson, et al.
Pageof 19

Showing results (61-70 of 188) with videos related to

Sort By:
Pageof 19
Molecular Vision|November 23, 2013
Clinical characteristics of early retinal disease due to CDHR1 mutationRola Ba-Abbad, Panagiotis I Sergouniotis, Vincent Plagnol, et al.
Retina (Philadelphia, Pa.)|March 12, 2011
Serial imaging and structure-function correlates of high-density rings of fundus autofluorescence in retinitis pigmentosaAnthony G Robson, Adnan Tufail, Fred Fitzke, et al.
Acta Ophthalmologica|January 8, 2013
Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration)Vasileios Soumplis, Panagiotis I Sergouniotis, Anthony G Robson, et al.
Acta Ophthalmologica|October 20, 2011
A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 genePanagiotis I Sergouniotis, Anthony G Robson, Zheng Li, et al.
Ophthalmic Genetics|August 14, 2020
Macula-predominant retinopathy associated with biallelic variants in <i>RDH12</i>Rola Ba-Abbad, Gavin Arno, Anthony G Robson, et al.
Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 3, 2023
ISCEV guidelines for calibration and verification of stimuli and recording instruments (2023 update)Daphne L McCulloch, Michael Bach, Mitchell Brigell, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 5, 2022
ISCEV Standard for full-field clinical electroretinography (2022 update)Anthony G Robson, Laura J Frishman, John Grigg, et al.
Ophthalmology|March 5, 2013
A phenotype-genotype correlation study of X-linked retinoschisisAjoy Vincent, Anthony G Robson, Magella M Neveu, et al.
Investigative Ophthalmology & Visual Science|July 28, 2004
Fundus autofluorescence in patients with leber congenital amaurosisHendrik P N Scholl, N H Victor Chong, Anthony G Robson, et al.
Pageof 19