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Andrew R Webster

Showing results (31-40 of 372) with videos related to

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Investigative Ophthalmology & Visual Science|July 1, 2011
A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosaAnna M Rose, Rajarshi Mukhopadhyay, Andrew R Webster, et al.
JAMA Ophthalmology|December 19, 2014
Clinical heterogeneity in a family with mutations in USH2AEva Lenassi, Anthony G Robson, Linda M Luxon, et al.
Clinical Ophthalmology (Auckland, N.Z.)|September 8, 2016
Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindnessJocelyn Cammack, John Whight, Vinette Cross, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|November 8, 2019
Benefit of an electronic head-mounted low vision aidMichael D Crossland, Sandra D Starke, Piotr Imielski, et al.
American Journal of Ophthalmology|July 25, 2021
Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated RetinopathyEvgenia Anikina, Michalis Georgiou, James Tee, et al.
Retina (Philadelphia, Pa.)|October 22, 2024
DIAGNOSTIC AND THERAPEUTIC CHALLENGESLandon J Rohowetz, Janet L Davis, Siying Lin, et al.
American Journal of Ophthalmology|October 6, 2012
Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1)Eva Lenassi, Eric Troeger, Robert Wilke, et al.
Investigative Ophthalmology & Visual Science|February 22, 2014
Visual consequences of molecular changes in the guanylate cyclase-activating proteinAndrew Stockman, G Bruce Henning, Anthony T Moore, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Clinical utility gene card for: choroideremiaMariya Moosajee, Simon C Ramsden, Graeme C M Black, et al.
Acta Ophthalmologica|December 30, 2014
Exome sequencing reveals ADAM9 mutations in a child with cone-rod dystrophySarah Hull, Gavin Arno, Vincent Plagnol, et al.
Pageof 38

Showing results (31-40 of 372) with videos related to

Sort By:
Pageof 38
Investigative Ophthalmology & Visual Science|July 1, 2011
A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosaAnna M Rose, Rajarshi Mukhopadhyay, Andrew R Webster, et al.
JAMA Ophthalmology|December 19, 2014
Clinical heterogeneity in a family with mutations in USH2AEva Lenassi, Anthony G Robson, Linda M Luxon, et al.
Clinical Ophthalmology (Auckland, N.Z.)|September 8, 2016
Psychophysical measures of visual function and everyday perceptual experience in a case of congenital stationary night blindnessJocelyn Cammack, John Whight, Vinette Cross, et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (Optometrists)|November 8, 2019
Benefit of an electronic head-mounted low vision aidMichael D Crossland, Sandra D Starke, Piotr Imielski, et al.
American Journal of Ophthalmology|July 25, 2021
Characterization of Retinal Function Using Microperimetry-Derived Metrics in Both Adults and Children With RPGR-Associated RetinopathyEvgenia Anikina, Michalis Georgiou, James Tee, et al.
Retina (Philadelphia, Pa.)|October 22, 2024
DIAGNOSTIC AND THERAPEUTIC CHALLENGESLandon J Rohowetz, Janet L Davis, Siying Lin, et al.
American Journal of Ophthalmology|October 6, 2012
Laser clearance of drusen deposit in patients with autosomal dominant drusen (p.Arg345Trp in EFEMP1)Eva Lenassi, Eric Troeger, Robert Wilke, et al.
Investigative Ophthalmology & Visual Science|February 22, 2014
Visual consequences of molecular changes in the guanylate cyclase-activating proteinAndrew Stockman, G Bruce Henning, Anthony T Moore, et al.
European Journal of Human Genetics : EJHG|August 22, 2013
Clinical utility gene card for: choroideremiaMariya Moosajee, Simon C Ramsden, Graeme C M Black, et al.
Acta Ophthalmologica|December 30, 2014
Exome sequencing reveals ADAM9 mutations in a child with cone-rod dystrophySarah Hull, Gavin Arno, Vincent Plagnol, et al.
Pageof 38