Showing results (91-100 of 456) with videos related to
Sort By:
Pageof 46
Clinical & Experimental Ophthalmology|June 3, 2011
Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye StudyJustin C Sherwin, John Kelly, Alex W Hewitt, et al.Clinical & Experimental Ophthalmology|October 23, 2018
Repurposing blue laser autofluorescence to measure ocular sun exposureGareth Lingham, Alex Burton, Holly A Brown, et al.Ophthalmic Genetics|October 20, 2006
Familial transmission risk of infantile glaucoma in AustraliaAlex W Hewitt, Jane R MacKinnon, Antonio Giubilato, et al.Human Mutation|June 21, 2007
A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteKathryn P Burdon, Shiwani Sharma, Celia S Chen, et al.Clinical & Experimental Optometry|August 23, 2022
Deep learning: applications in retinal and optic nerve diseasesJason Charng, Khyber Alam, Gavin Swartz, et al.Translational Vision Science & Technology|December 16, 2017
Intersession Test-Retest Variability of Microperimetry in Type 2 Macular TelangiectasiaEvan N Wong, Jehan D A De Soyza, David A Mackey, et al.BMJ Open Ophthalmology|June 11, 2019
Traumatic hyphaema in children: a retrospective and prospective study of outcomes at an Australian paediatric centreMichael D Richards, Kate Barnes, Anne-Marie E Yardley, et al.Medrxiv : the Preprint Server for Health Sciences|February 23, 2026
Genome-wide association study of corneal dystrophy uncovers novel risk loci and enables improved polygenic prediction of Fuchs endothelial corneal dystrophyBenyapa Insawang, David A Mackey, Alex W Hewitt, et al.Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|December 5, 2002
Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutationsNeil Howell, Neil R Miller, David A Mackey, et al.JAMA Ophthalmology|April 21, 2022
Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on AgingWeixiong He, Xikun Han, Jue-Sheng Ong, et al.Pageof 46