Michaelides M - Search Results

1

Genetic treatment for autosomal dominant inherited retinal dystrophies: approaches, challenges and targeted genotypes.

Daich Varela M, Georgiadis A, Michaelides M. Daich Varela M, et al. Among authors: michaelides m. Br J Ophthalmol. 2023 Sep;107(9):1223-1230. doi: 10.1136/bjo-2022-321903. Epub 2022 Aug 29. Br J Ophthalmol. 2023. PMID: 36038193 Review.

2

A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.

Michaelides M, Holder GE, Hunt DM, Fitzke FW, Bird AC, Moore AT. Michaelides M, et al. Br J Ophthalmol. 2005 Feb;89(2):198-206. doi: 10.1136/bjo.2004.050773. Br J Ophthalmol. 2005. PMID: 15665353 Free PMC article.

3

Progressive cone and cone-rod dystrophies: phenotypes and underlying molecular genetic basis.

Michaelides M, Hardcastle AJ, Hunt DM, Moore AT. Michaelides M, et al. Surv Ophthalmol. 2006 May-Jun;51(3):232-58. doi: 10.1016/j.survophthal.2006.02.007. Surv Ophthalmol. 2006. PMID: 16644365 Review.

4

Characterisation of the macular dystrophy in patients with the A3243G mitochondrial DNA point mutation with fundus autofluorescence.

Rath PP, Jenkins S, Michaelides M, Smith A, Sweeney MG, Davis MB, Fitzke FW, Bird AC. Rath PP, et al. Among authors: michaelides m. Br J Ophthalmol. 2008 May;92(5):623-9. doi: 10.1136/bjo.2007.131177. Br J Ophthalmol. 2008. PMID: 18441172 Free PMC article.

5

High-resolution optical coherence tomography imaging in KCNV2 retinopathy.

Sergouniotis PI, Holder GE, Robson AG, Michaelides M, Webster AR, Moore AT. Sergouniotis PI, et al. Among authors: michaelides m. Br J Ophthalmol. 2012 Feb;96(2):213-7. doi: 10.1136/bjo.2011.203638. Epub 2011 May 10. Br J Ophthalmol. 2012. PMID: 21558291

6

Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2.

Subash M, Rotsos T, Wright GA, Devery S, Holder GE, Robson AG, Pal B, Tufail A, Webster AR, Moore AT, Michaelides M. Subash M, et al. Among authors: michaelides m. Br J Ophthalmol. 2012 May;96(5):719-22. doi: 10.1136/bjophthalmol-2011-300964. Epub 2011 Dec 15. Br J Ophthalmol. 2012. PMID: 22174098

7

Developmental macular disorders: phenotypes and underlying molecular genetic basis.

Michaelides M, Jeffery G, Moore AT. Michaelides M, et al. Br J Ophthalmol. 2012 Jul;96(7):917-24. doi: 10.1136/bjophthalmol-2011-300994. Epub 2012 Apr 19. Br J Ophthalmol. 2012. PMID: 22517799 Review.

8

Retinal structure and function in achromatopsia: implications for gene therapy.

Sundaram V, Wilde C, Aboshiha J, Cowing J, Han C, Langlo CS, Chana R, Davidson AE, Sergouniotis PI, Bainbridge JW, Ali RR, Dubra A, Rubin G, Webster AR, Moore AT, Nardini M, Carroll J, Michaelides M. Sundaram V, et al. Among authors: michaelides m. Ophthalmology. 2014 Jan;121(1):234-245. doi: 10.1016/j.ophtha.2013.08.017. Epub 2013 Oct 20. Ophthalmology. 2014. PMID: 24148654 Free PMC article.

9

Clinical and molecular characteristics of childhood-onset Stargardt disease.

Fujinami K, Zernant J, Chana RK, Wright GA, Tsunoda K, Ozawa Y, Tsubota K, Robson AG, Holder GE, Allikmets R, Michaelides M, Moore AT. Fujinami K, et al. Among authors: michaelides m. Ophthalmology. 2015 Feb;122(2):326-34. doi: 10.1016/j.ophtha.2014.08.012. Epub 2014 Oct 12. Ophthalmology. 2015. PMID: 25312043 Free PMC article.

10

The cone dysfunction syndromes.

Aboshiha J, Dubis AM, Carroll J, Hardcastle AJ, Michaelides M. Aboshiha J, et al. Among authors: michaelides m. Br J Ophthalmol. 2016 Jan;100(1):115-21. doi: 10.1136/bjophthalmol-2014-306505. Epub 2015 Mar 13. Br J Ophthalmol. 2016. PMID: 25770143 Free PMC article. Review.

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