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Journal of Glaucoma|June 5, 2003
Tonography demonstrates reduced facility of outflow of aqueous humor in myocilin mutation carriersColleen H Wilkinson, David van der Straaten, Jamie E Craig, et al.Molecular Vision|December 20, 2008
Evaluation of splicing efficiency in lymphoblastoid cell lines from patients with splicing-factor retinitis pigmentosaLenka Ivings, Katherine V Towns, M A Matin, et al.Journal of Glaucoma|April 15, 2020
Do Levels of Stress Markers Influence the Retinal Nerve Fiber Layer Thickness in Young Adults?Samantha Sze-Yee Lee, Paul G Sanfilippo, Seyhan Yazar, et al.Investigative Ophthalmology & Visual Science|May 28, 2010
Automated quantification of inherited phenotypes from color images: a twin study of the variability of optic nerve head shapeLi Tang, Todd E Scheetz, David A Mackey, et al.Plos One|September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern AustraliaAlpana Dave, Kate Laurie, Sandra E Staffieri, et al.Mitochondrion|July 21, 2020
OXPHOS bioenergetic compensation does not explain disease penetrance in Leber hereditary optic neuropathyM Isabel G Lopez Sanchez, Nicole J Van Bergen, Lisa S Kearns, et al.JAMA Ophthalmology|November 23, 2013
Common mechanisms underlying refractive error identified in functional analysis of gene lists from genome-wide association study results in 2 European British cohortsPirro G Hysi, Omar A Mahroo, Phillippa Cumberland, et al.Ophthalmology. Retina|May 14, 2022
Prevalence of Toxoplasmic Retinochoroiditis in an Australian Adult Population: A Community-Based StudyLisia B Ferreira, João M Furtado, Jason Charng, et al.Plos One|July 7, 2011
Mitochondrial oxidative phosphorylation compensation may preserve vision in patients with OPA1-linked autosomal dominant optic atrophyNicole J Van Bergen, Jonathan G Crowston, Lisa S Kearns, et al.Cornea|December 8, 2011
Role of the TCF4 gene intronic variant in normal variation of corneal endotheliumDavid A Mackey, Nicole M Warrington, Alex W Hewitt, et al.Pageof 46