Michel Michaelides
UCL Institute of Ophthalmology
11-43 Bath Street
London EC1V 9EL
UK;
Name/email consistency: high
- Developmental macular disorders: phenotypes and underlying molecular genetic basis. Michaelides, M., Jeffery, G., Moore, A.T. Br. J. Ophthalmol (2012)
- The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy. Michaelides, M., Gaillard, M.C., Escher, P., Tiab, L., Bedell, M., Borruat, F.X., Barthelmes, D., Carmona, R., Zhang, K., White, E., McClements, M., Robson, A.G., Holder, G.E., Bradshaw, K., Hunt, D.M., Webster, A.R., Moore, A.T., Schorderet, D.F., Munier, F.L. Invest. Ophthalmol. Vis. Sci. (2010)
- A prospective randomized trial of intravitreal bevacizumab or laser therapy in the management of diabetic macular edema (BOLT study) 12-month data: report 2. Michaelides, M., Kaines, A., Hamilton, R.D., Fraser-Bell, S., Rajendram, R., Quhill, F., Boos, C.J., Xing, W., Egan, C., Peto, T., Bunce, C., Leslie, R.D., Hykin, P.G. Ophthalmology (2010)
- Macular dystrophy associated with the A3243G mitochondrial DNA mutation. Distinct retinal and associated features, disease variability, and characterization of asymptomatic family members. Michaelides, M., Jenkins, S.A., Bamiou, D.E., Sweeney, M.G., Davis, M.B., Luxon, L., Bird, A.C., Rath, P.P. Arch. Ophthalmol. (2008)
- Glaucoma following congenital cataract surgery--the role of early surgery and posterior capsulotomy. Michaelides, M., Bunce, C., Adams, G.G. BMC. Ophthalmol (2007)
- Evidence of genetic heterogeneity in MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome. Michaelides, M., Urquhart, J., Holder, G.E., Restori, M., Kayali, N., Manson, F.D., Black, G.C. Am. J. Ophthalmol. (2006)









