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David A Mackey

Showing results (111-120 of 498) with videos related to

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Acta Ophthalmologica|January 15, 2015
Distribution of astigmatism as a function of age in an Australian populationPaul G Sanfilippo, Seyhan Yazar, Lisa Kearns, et al.
Journal of Clinical Medicine|August 4, 2015
iPS Cells for Modelling and Treatment of Retinal DiseasesFred K Chen, Samuel McLenachan, Michael Edel, et al.
Ergonomics|December 22, 2018
Mobile touch screen device use and associations with musculoskeletal symptoms and visual health in a nationally representative sample of Singaporean adolescentsSiao Hui Toh, Pieter Coenen, Erin K Howie, et al.
Clinical & Experimental Ophthalmology|October 23, 2004
Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 18, 2026
Multi-Ancestry, Multitrait Polygenic Risk Scores for Myopia: Improved Accuracy and Clinical PotentialBenyapa Insawang, Guiyan Ni, Nicholas Clark, et al.
American Journal of Ophthalmology|October 18, 2005
A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma familiesPaul N Baird, Andrea J Richardson, David A Mackey, et al.
Translational Vision Science & Technology|January 26, 2018
Intrasession Repeatability and Interocular Symmetry of Foveal Avascular Zone and Retinal Vessel Density in OCT AngiographyFred K Chen, Moreno Menghini, Alex Hansen, et al.
Clinical & Experimental Ophthalmology|October 15, 2020
Improving parents' knowledge of early signs of paediatric eye disease: A double-blind randomized controlled trialSandra E Staffieri, Gwyneth Rees, Paul G Sanfilippo, et al.
Ophthalmic Genetics|April 13, 2005
Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pterAmy C Cohn, Lisa S Kearns, Ravi Savarirayan, et al.
American Journal of Ophthalmology|June 15, 2005
The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Pageof 50

Showing results (111-120 of 498) with videos related to

Sort By:
Pageof 50
Acta Ophthalmologica|January 15, 2015
Distribution of astigmatism as a function of age in an Australian populationPaul G Sanfilippo, Seyhan Yazar, Lisa Kearns, et al.
Journal of Clinical Medicine|August 4, 2015
iPS Cells for Modelling and Treatment of Retinal DiseasesFred K Chen, Samuel McLenachan, Michael Edel, et al.
Ergonomics|December 22, 2018
Mobile touch screen device use and associations with musculoskeletal symptoms and visual health in a nationally representative sample of Singaporean adolescentsSiao Hui Toh, Pieter Coenen, Erin K Howie, et al.
Clinical & Experimental Ophthalmology|October 23, 2004
Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|May 18, 2026
Multi-Ancestry, Multitrait Polygenic Risk Scores for Myopia: Improved Accuracy and Clinical PotentialBenyapa Insawang, Guiyan Ni, Nicholas Clark, et al.
American Journal of Ophthalmology|October 18, 2005
A common disease haplotype for the Q368STOP mutation of the myocilin gene in Australian and Canadian glaucoma familiesPaul N Baird, Andrea J Richardson, David A Mackey, et al.
Translational Vision Science & Technology|January 26, 2018
Intrasession Repeatability and Interocular Symmetry of Foveal Avascular Zone and Retinal Vessel Density in OCT AngiographyFred K Chen, Moreno Menghini, Alex Hansen, et al.
Clinical & Experimental Ophthalmology|October 15, 2020
Improving parents' knowledge of early signs of paediatric eye disease: A double-blind randomized controlled trialSandra E Staffieri, Gwyneth Rees, Paul G Sanfilippo, et al.
Ophthalmic Genetics|April 13, 2005
Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pterAmy C Cohn, Lisa S Kearns, Ravi Savarirayan, et al.
American Journal of Ophthalmology|June 15, 2005
The Q368STOP myocilin mutation in a population-based cohort: the Blue Mountains Eye StudyPaul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Pageof 50