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Phenotypic variation in enhanced S-cone syndrome.
Audo I, Michaelides M, Robson AG, Hawlina M, Vaclavik V, Sandbach JM, Neveu MM, Hogg CR, Hunt DM, Moore AT, Bird AC, Webster AR, Holder GE. Audo I, et al. Among authors: robson ag. Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93. doi: 10.1167/iovs.05-1629. Invest Ophthalmol Vis Sci. 2008. PMID: 18436841
A phenotype-genotype correlation study of X-linked retinoschisis.
Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE. Vincent A, et al. Among authors: robson ag. Ophthalmology. 2013 Jul;120(7):1454-64. doi: 10.1016/j.ophtha.2012.12.008. Epub 2013 Feb 28. Ophthalmology. 2013. PMID: 23453514
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variants.
Gardner JC, Liew G, Quan YH, Ermetal B, Ueyama H, Davidson AE, Schwarz N, Kanuga N, Chana R, Maher ER, Webster AR, Holder GE, Robson AG, Cheetham ME, Liebelt J, Ruddle JB, Moore AT, Michaelides M, Hardcastle AJ. Gardner JC, et al. Among authors: robson ag. Hum Mutat. 2014 Nov;35(11):1354-62. doi: 10.1002/humu.22679. Hum Mutat. 2014. PMID: 25168334 Free PMC article.
The Natural History of the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Studies: Design and Baseline Characteristics: ProgStar Report No. 1.
Strauss RW, Ho A, Muñoz B, Cideciyan AV, Sahel JA, Sunness JS, Birch DG, Bernstein PS, Michaelides M, Traboulsi EI, Zrenner E, Sadda S, Ervin AM, West S, Scholl HP; Progression of Stargardt Disease Study Group. Strauss RW, et al. Ophthalmology. 2016 Apr;123(4):817-28. doi: 10.1016/j.ophtha.2015.12.009. Epub 2016 Jan 16. Ophthalmology. 2016. PMID: 26786511
207 results