Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy von Gill, Jasdeep S, Georgiou, Michalis, Kalitzeos, Angelos, Moore, Anthony T, Michaelides, Michel

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Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups von Parfitt, David A., Lane, Amelia, Ramsden, Conor M., Carr, Amanda-Jayne F., Munro, Peter M., Jovanovic, Katarina, Schwarz, Nele, Kanuga, Naheed, Muthiah, Manickam N., Hull, Sarah, Gallo, Jean-Marc, da Cruz, Lyndon, Moore, Anthony T., Hardcastle, Alison J., Coffey, Peter J., Cheetham, Michael E.

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The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapies von De Silva, Samantha R., Arno, Gavin, Robson, Anthony G., Fakin, Ana, Pontikos, Nikolas, Mohamed, Moin D., Bird, Alan C., Moore, Anthony T., Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.

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Genetic Testing for Inherited Retinal Disease von Moore, Anthony T.

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Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease von Fujinami, Kaoru, MD, Zernant, Jana, MS, Chana, Ravinder K., BSc, Wright, Genevieve A., BSc, Tsunoda, Kazushige, MD, PhD, Ozawa, Yoko, MD, PhD, Tsubota, Kazuo, MD, PhD, Robson, Anthony G., PhD, Holder, Graham E., PhD, Allikmets, Rando, PhD, Michaelides, Michel, MD, FRCOphth, Moore, Anthony T., FRCS, FRCOphth

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Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom von Pontikos, Nikolas, Arno, Gavin, Jurkute, Neringa, Schiff, Elena, Ba-Abbad, Rola, Malka, Samantha, Gimenez, Ainoa, Georgiou, Michalis, Wright, Genevieve, Armengol, Monica, Knight, Hannah, Katz, Menachem, Moosajee, Mariya, Yu-Wai-Man, Patrick, Moore, Anthony T., Michaelides, Michel, Webster, Andrew R., Mahroo, Omar A.

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Optogenetic approaches to therapy for inherited retinal degenerations von De Silva, Samantha R., Moore, Anthony T.

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Valproate administered after traumatic brain injury provides neuroprotection and improves cognitive function in rats von Dash, Pramod K, Orsi, Sara A, Zhang, Min, Grill, Raymond J, Pati, Shibani, Zhao, Jing, Moore, Anthony N

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John Hunter: Personal and professional inspiration from the sovereign of surgery von Moore, Anthony R. (Tony)

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Mitochondrial Disorders and the Eye: A New Era for Diagnosis von Moore, Anthony T, Yu-Wai-Man, Patrick

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WITHDRAWN: There is often - But not always - An alternative von Jacobs, Howard T, Moore, Anthony L

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There is often – but not always – an alternative von Jacobs, Howard T., Moore, Anthony L.

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Prediction of drug-induced mitochondrial dysfunction using succinate-cytochrome c reductase activity, QSAR and molecular docking von Rosell-Hidalgo, Alicia, Moore, Anthony L., Ghafourian, Taravat

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Xenotopic expression of alternative oxidase (AOX) to study mechanisms of mitochondrial disease von Viscomi, Carlo, Moore, Anthony L., Zeviani, Massimo, Szibor, Marten

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100,000 Genomes Pilot on Rare-Disease Diagnosis in Health Care — Preliminary Report von Smedley, Damian, Smith, Katherine R, Martin, Antonio, Thomas, Ellen A, McDonagh, Ellen M, Cipriani, Valentina, Ellingford, Jamie M, Arno, Gavin, Tucci, Arianna, Vandrovcova, Jana, Chan, Georgia, Williams, Hywel J, Ratnaike, Thiloka, Wei, Wei, Stirrups, Kathleen, Ibanez, Kristina, Moutsianas, Loukas, Wielscher, Matthias, Need, Anna, Barnes, Michael R, Vestito, Letizia, Buchanan, James, Wordsworth, Sarah, Ashford, Sofie, Rehmström, Karola, Li, Emily, Fuller, Gavin, Twiss, Philip, Spasic-Boskovic, Olivera, Halsall, Sally, Floto, R Andres, Poole, Kenneth, Wagner, Annette, Mehta, Sarju G, Gurnell, Mark, Burrows, Nigel, James, Roger, Penkett, Christopher, Dewhurst, Eleanor, Gräf, Stefan, Mapeta, Rutendo, Kasanicki, Mary, Haworth, Andrea, Savage, Helen, Babcock, Melanie, Reese, Martin G, Bale, Mark, Baple, Emma, Boustred, Christopher, Brittain, Helen, de Burca, Anna, Bleda, Marta, Devereau, Andrew, Halai, Dina, Haraldsdottir, Eik, Hyder, Zerin, Kasperaviciute, Dalia, Patch, Christine, Polychronopoulos, Dimitris, Matchan, Angela, Sultana, Razvan, Ryten, Mina, Tavares, Ana L T, Tregidgo, Carolyn, Turnbull, Clare, Welland, Matthew, Wood, Suzanne, Snow, Catherine, Williams, Eleanor, Leigh, Sarah, Foulger, Rebecca E, Daugherty, Louise C, Niblock, Olivia, Leong, Ivone U S, Wright, Caroline F, Davies, Jim, Crichton, Charles, Welch, James, Woods, Kerrie, Abulhoul, Lara, Aurora, Paul, Bockenhauer, Detlef, Broomfield, Alexander, Cleary, Maureen A, Lam, Tanya, Dattani, Mehul, Footitt, Emma, Ganesan, Vijeya, Grunewald, Stephanie, Compeyrot-Lacassagne, Sandrine, Muntoni, Francesco, Pilkington, Clarissa, Quinlivan, Rosaline, Thapar, Nikhil, Wallis, Colin, Wedderburn, Lucy R, Worth, Austen, Bueser, Teofila, Compton, Cecilia, Deshpande, Charu

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Congenital focal abnormalities of the retina and retinal pigment epithelium von Liu, Yingna, Moore, Anthony T.

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Prevalence of cystoid macular oedema, epiretinal membrane and cataract in retinitis pigmentosa von Liew, Gerald, Strong, Stacey, Bradley, Patrick, Severn, Philip, Moore, Anthony T, Webster, Andrew R, Mitchell, Paul, Kifley, Annette, Michaelides, Michel

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Clinical and Genetic Features of Choroideremia in Childhood von Khan, Kamron N., PhD, FRCOphth, Islam, Farrah, FCPS, FRCS, Moore, Anthony T., FRCS, FRCOphth, Michaelides, Michel, MD(Res), FRCOphth

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Early Patterns of Macular Degeneration in ABCA4-Associated Retinopathy von Khan, Kamron N., Kasilian, Melissa, Mahroo, Omar A.R., Tanna, Preena, Kalitzeos, Angelos, Robson, Anthony G., Tsunoda, Kazushige, Iwata, Takeshi, Moore, Anthony T., Fujinami, Kaoru, Michaelides, Michel

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Unraveling the heater: new insights into the structure of the alternative oxidase von Moore, Anthony L, Shiba, Tomoo, Young, Luke, Harada, Shigeharu, Kita, Kiyoshi, Ito, Kikukatsu

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