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R A Parry

Showing results (71-80 of 77) with videos related to

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Journal of the Optical Society of America. A, Optics, Image Science, and Vision|August 12, 2025
Color Vision 2025: Introduction by the feature editorsSérgio M C Nascimento, David H Foster, Paul R Martin, et al.
American Journal of Ophthalmology|August 22, 2016
Automated Measurement of Visual Acuity in Pediatric Ophthalmic Patients Using Principles of Game Design and Tablet ComputersTariq M Aslam, Humza J Tahir, Neil R A Parry, et al.
Acta Ophthalmologica|May 28, 2022
Clinical and genetic findings in TRPM1-related congenital stationary night blindnessChristos Iosifidis, Jingshu Liu, Theodora Gale, et al.
Investigative Ophthalmology & Visual Science|January 10, 2015
Abrogation of HMX1 function causes rare oculoauricular syndrome associated with congenital cataract, anterior segment dysgenesis, and retinal dystrophyRachel L Gillespie, Jill Urquhart, Simon C Lovell, et al.
Plos One|March 19, 2015
The spatial properties of L- and M-cone inputs to electroretinograms that reflect different types of post-receptoral processingMellina M Jacob, Gobinda Pangeni, Bruno D Gomes, et al.
Scientific Reports|November 14, 2019
Clinical and genetic variability in children with partial albinismPatrick Campbell, Jamie M Ellingford, Neil R A Parry, et al.
Ophthalmology|March 26, 2017
Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal DiseaseRachel L Taylor, Neil R A Parry, Stephanie J Barton, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Journal of the Optical Society of America. A, Optics, Image Science, and Vision|August 12, 2025
Color Vision 2025: Introduction by the feature editorsSérgio M C Nascimento, David H Foster, Paul R Martin, et al.
American Journal of Ophthalmology|August 22, 2016
Automated Measurement of Visual Acuity in Pediatric Ophthalmic Patients Using Principles of Game Design and Tablet ComputersTariq M Aslam, Humza J Tahir, Neil R A Parry, et al.
Acta Ophthalmologica|May 28, 2022
Clinical and genetic findings in TRPM1-related congenital stationary night blindnessChristos Iosifidis, Jingshu Liu, Theodora Gale, et al.
Investigative Ophthalmology & Visual Science|January 10, 2015
Abrogation of HMX1 function causes rare oculoauricular syndrome associated with congenital cataract, anterior segment dysgenesis, and retinal dystrophyRachel L Gillespie, Jill Urquhart, Simon C Lovell, et al.
Plos One|March 19, 2015
The spatial properties of L- and M-cone inputs to electroretinograms that reflect different types of post-receptoral processingMellina M Jacob, Gobinda Pangeni, Bruno D Gomes, et al.
Scientific Reports|November 14, 2019
Clinical and genetic variability in children with partial albinismPatrick Campbell, Jamie M Ellingford, Neil R A Parry, et al.
Ophthalmology|March 26, 2017
Panel-Based Clinical Genetic Testing in 85 Children with Inherited Retinal DiseaseRachel L Taylor, Neil R A Parry, Stephanie J Barton, et al.
Pageof 8