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Acta Ophthalmologica
|
January 15, 2015
Distribution of astigmatism as a function of age in an Australian population
Paul G Sanfilippo, Seyhan Yazar, Lisa Kearns, et al.
Journal of Clinical Medicine
|
August 4, 2015
iPS Cells for Modelling and Treatment of Retinal Diseases
Fred 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 adolescents
Siao 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 Study
Paul 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 Potential
Benyapa 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 families
Paul 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 Angiography
Fred 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 trial
Sandra 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-pter
Amy 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 Study
Paul N Baird, Andrea J Richardson, Jamie E Craig, et al.
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of 50
Search research articles
Search
Showing results (111-120 of 498) with videos related to
Sort By:
Page
of 50
Acta Ophthalmologica
|
January 15, 2015
Distribution of astigmatism as a function of age in an Australian population
Paul G Sanfilippo, Seyhan Yazar, Lisa Kearns, et al.
Journal of Clinical Medicine
|
August 4, 2015
iPS Cells for Modelling and Treatment of Retinal Diseases
Fred 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 adolescents
Siao 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 Study
Paul 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 Potential
Benyapa 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 families
Paul 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 Angiography
Fred 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 trial
Sandra 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-pter
Amy 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 Study
Paul N Baird, Andrea J Richardson, Jamie E Craig, et al.
Page
of 50