Residual cone vision without alpha-transducin. by Stockman, A, Smithson, H, Michaelides, M, Moore, A, Webster, A, Sharpe, LT

Residual cone vision without alpha-transducin. by Stockman, A, Smithson, H, Michaelides, M, Moore, A, Webster, A, Sharpe, LT

X-linked cone dysfunction syndrome with myopia and protanopia. by Michaelides, M, Johnson, S, Bradshaw, K, Holder, G, Simunovic, M, Mollon, J, Moore, A, Hunt, D

Blue cone monochromatism: a phenotype and genotype assessment with evidence of progressive loss of cone function in older individuals. by Michaelides, M, Johnson, S, Simunovic, M, Bradshaw, K, Holder, G, Mollon, J, Moore, A, Hunt, D

"Cone dystrophy with supernormal rod electroretinogram": a comprehensive genotype/phenotype study including fundus autofluorescence and extensive electrophysiology. by Robson, A, Webster, A, Michaelides, M, Downes, S, Cowing, J, Hunt, D, Moore, A, Holder, G

The Impact of Inherited Retinal Diseases in the Republic of Ireland (ROI) and the United Kingdom (UK) from a Cost-of-Illness Perspective by Galvin O, Chi G, Brady L, Hippert C, Del Valle Rubido M, Daly A, Michaelides M

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Cone dystrophy phenotype associated with a frameshift mutation (M280fsX291) in the alpha-subunit of cone specific transducin (GNAT2). by Michaelides, M, Aligianis, I, Holder, G, Simunovic, M, Mollon, J, Maher, E, Hunt, D, Moore, A

Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. by McClements, M, Davies, W, Michaelides, M, Young, T, Neitz, M, MacLaren, R, Moore, A, Hunt, D

Correlating reactivity and selectivity to cyclopentadienyl ligand properties in Rh(III)-catalyzed C-H activation reactions: an experimental and computational study by Piou, T, Romanov-Michailidis, F, Romanova-Michaelides, M, Jackson, K, Semakul, N, Taggart, T, Newell, B, Rithner, C, Paton, R, Rovis, T

A randomized controlled trial comparing everting sutures with everting sutures and a lateral tarsal strip for involutional entropion by Scheepers, M.A., Singh, R., Ng, J., Zuercher, D., Gibson, A., Bunce, C., Fong, K., Michaelides, M., Olver, J.

Characterization of CDH3-related congenital hypotrichosis with juvenile macular dystrophy by Hull, S, Arno, G, Robson, A, Broadgate, S, Plagnol, V, McKibbin, M, Halford, S, Michaelides, M, Holder, G, Moore, A, Khan, K, Webster, A

X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene. by McClements, M, Davies, W, Michaelides, M, Carroll, J, Rha, J, Mollon, J, Neitz, M, MacLaren, R, Moore, A, Hunt, D

Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy. by Halford, S, Liew, G, Mackay, D, Sergouniotis, P, Holt, R, Broadgate, S, Volpi, E, Ocaka, L, Robson, A, Holder, G, Moore, A, Michaelides, M, Webster, A

Childhood-onset Leber hereditary optic neuropathy by Majander, A, Bowman, R, Poulton, J, Antcliff, R, Reddy, M, Michaelides, M, Webster, A, Chinnery, P, Votruba, M, Moore, A, Yu-Wai-Man, P

Detailed phenotypic and genotypic characterization of bietti crystalline dystrophy by Halford, S, Liew, G, MacKay, D, Sergouniotis, P, Holt, R, Broadgate, S, Volpi, E, Ocaka, L, Robson, A, Holder, G, Moore, A, Michaelides, M, Webster, A

Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy. by Arrigoni, F, Matarin, M, Thompson, P, Michaelides, M, Mcclements, M, Redmond, E, Clarke, L, Ellins, E, Mohamed, S, Pavord, I, Klein, N, Hunt, D, Moore, A, Halcox, J, Sisodiya, S

Erratum: Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophy (European Journal of Human Genetics (2011) 19 (131-137) DOI:10... by Arrigoni, F, Matarin, M, Thompson, P, Michaelides, M, McClements, M, Redmond, E, Clarke, L, Ellins, E, Mohamed, S, Pavord, I, Klein, N, Hunt, D, Moore, A, Halcox, J, Sisodiya, S

Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen. by Taylor, RL, Poulter, JA, Downes, SM, McKibbin, M, Khan, KN, Inglehearn, CF, Webster, AR, Hardcastle, AJ, Michaelides, M, Bishop, PN, Clark, SJ, Black, GC, United Kingdom Inherited Retinal Dystrophy Consortium, Halford, S

Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa by Fiorentino, A, Yu, J, Arno, G, Pontikos, N, Halford, S, Broadgate, S, Michaelides, M, Carss, K, Raymond, F, Cheetham, M, Webster, A, Downes, S, Hardcastle, A, NIHR-BioResource Rare Diseases Consortium, UK Inherited Retinal Dystrophy Consortium

Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy. by Tan, M, Mackay, D, Cowing, J, Tran, H, Smith, A, Wright, G, Dev-Borman, A, Henderson, R, Moradi, P, Russell-Eggitt, I, Maclaren, R, Robson, A, Cheetham, M, Thompson, D, Webster, A, Michaelides, M, Ali, R, Moore, A