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WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease Progression.
Majander A, Jurkute N, Burté F, Brock K, João C, Huang H, Neveu MM, Chan CM, Duncan HJ, Kelly S, Burkitt-Wright E, Khoyratty F, Lai YT, Subash M, Chinnery PF, Bitner-Glindzicz M, Arno G, Webster AR, Moore AT, Michaelides M, Stockman A, Robson AG, Yu-Wai-Man P. Majander A, et al. Among authors: neveu mm. Am J Ophthalmol. 2022 Sep;241:9-27. doi: 10.1016/j.ajo.2022.04.003. Epub 2022 Apr 22. Am J Ophthalmol. 2022. PMID: 35469785 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: neveu mm. 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: neveu mm. 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
Electroretinogram measures in a septuagenarian population.
Neveu MM, Dangour A, Allen E, Robson AG, Bird AC, Uauy R, Holder GE. Neveu MM, et al. Doc Ophthalmol. 2011 Oct;123(2):75-81. doi: 10.1007/s10633-011-9282-1. Epub 2011 Aug 4. Doc Ophthalmol. 2011. PMID: 21814827
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: neveu mm. Ophthalmology. 2013 Jul;120(7):1454-64. doi: 10.1016/j.ophtha.2012.12.008. Epub 2013 Feb 28. Ophthalmology. 2013. PMID: 23453514
Isolated rod dysfunction associated with a novel genotype of CNGB1.
Ba-Abbad R, Holder GE, Robson AG, Neveu MM, Waseem N, Arno G, Webster AR. Ba-Abbad R, et al. Among authors: neveu mm. Am J Ophthalmol Case Rep. 2019 Mar 19;14:83-86. doi: 10.1016/j.ajoc.2019.03.004. eCollection 2019 Jun. Am J Ophthalmol Case Rep. 2019. PMID: 30976726 Free PMC article.
Juvenile Batten Disease (CLN3): Detailed Ocular Phenotype, Novel Observations, Delayed Diagnosis, Masquerades, and Prospects for Therapy.
Wright GA, Georgiou M, Robson AG, Ali N, Kalhoro A, Holthaus SK, Pontikos N, Oluonye N, de Carvalho ER, Neveu MM, Weleber RG, Michaelides M. Wright GA, et al. Among authors: neveu mm. Ophthalmol Retina. 2020 Apr;4(4):433-445. doi: 10.1016/j.oret.2019.11.005. Epub 2019 Nov 13. Ophthalmol Retina. 2020. PMID: 31926949 Free PMC article.
39 results