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Page 1
Loss of sheen in Oguchi disease following short wavelength exposure.
Akhtar HN, Nicholson L, Ockrim Z, Neveu M, Webster AR, Michaelides M, Mahroo OA. Akhtar HN, et al. Among authors: webster ar. Eye (Lond). 2024 Nov;38(16):3197-3199. doi: 10.1038/s41433-024-03237-4. Epub 2024 Jul 14. Eye (Lond). 2024. PMID: 39003433 Free PMC article. No abstract available.
Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause "cone dystrophy with supernormal rod electroretinogram" in humans.
Wu H, Cowing JA, Michaelides M, Wilkie SE, Jeffery G, Jenkins SA, Mester V, Bird AC, Robson AG, Holder GE, Moore AT, Hunt DM, Webster AR. Wu H, et al. Among authors: webster ar. Am J Hum Genet. 2006 Sep;79(3):574-9. doi: 10.1086/507568. Epub 2006 Jul 24. Am J Hum Genet. 2006. PMID: 16909397 Free PMC article.
Residual cone vision without alpha-transducin.
Stockman A, Smithson HE, Michaelides M, Moore AT, Webster AR, Sharpe LT. Stockman A, et al. Among authors: webster ar. J Vis. 2007 Mar 23;7(4):8. doi: 10.1167/7.4.8. J Vis. 2007. PMID: 17461692 Free article.
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: webster ar. Invest Ophthalmol Vis Sci. 2008 May;49(5):2082-93. doi: 10.1167/iovs.05-1629. Invest Ophthalmol Vis Sci. 2008. PMID: 18436841
Clinicopathological case series of four patients with inherited macular disease.
Wickham L, Chen FK, Lewis GP, Uppal GS, Neveu MM, Wright GA, Robson AG, Webster AR, Grierson I, Hiscott P, Coffey PJ, Holder GE, Fisher SK, Da Cruz L. Wickham L, et al. Among authors: webster ar. Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3553-61. doi: 10.1167/iovs.08-2715. Epub 2009 Mar 11. Invest Ophthalmol Vis Sci. 2009. PMID: 19279306
381 results