Colour discrimination ellipses in patients with dominant optic atrophy by Simunovic, M, Votruba, M, Regan, B, Mollon, J

Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophy by Perganta, G, Barnard, A, Katti, C, Vachtsevanos, A, Douglas, R, Maclaren, R, Votruba, M, Sekaran, S

Specific deficits in visual electrophysiology in a mouse model of dominant optic atrophy. by Barnard, A, Charbel Issa, P, Perganta, G, Williams, P, Davies, V, Sekaran, S, Votruba, M, Maclaren, R

Specific deficits in visual electrophysiology in a mouse model of dominant optic atrophy by Barnard, A, Issa, P, Perganta, G, Williams, P, Davies, V, Sekaran, S, Votruba, M, MacLaren, R

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

Validating the RedMIT/GFP-LC3 mouse model by studying mitophagy in autosomal dominant optic atrophy due to the OPA1Q285STOP mutation by Diot, A, Agnew, T, Sanderson, J, Liao, C, Carver, J, Neves, R, Gupta, R, Guo, Y, Waters, C, Seto, S, Daniels, M, Dombi, E, Lodge, T, Morten, K, Williams, S, Enver, T, Iborra, F, Votruba, M, Poulton, J

Dysregulated mitophagy and mitochondrial transport in severe dominant optic atrophy due to OPA1 mutations by Liao, C, Ashley, N, Morten, K, Phadwal, K, Williams, A, Fearnley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D, Vay, L, Quaghebeur, G, Macleod, L, Gabriel, A, Downes, S, Simon, K, Votruba, M, Poulton, J

Dysregulated mitophagy and mitochondrial transport in severe inherited optic atrophy due to OPA1 mutations by Poulton, J, Liao, C, Ashley, N, Morten, K, Phadwal, K, Williams, A, Feamley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Macleod, L, Downes, S, Zeviani, M, Simon, A, Votruba, M

Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations. by Liao, C, Ashley, N, Diot, A, Morten, K, Phadwal, K, Williams, A, Fearnley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D, Vay, L, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Downes, S, Sitarz, K, Flannery, P, Carver, J, Dombi, E, East, D, Laura, M, Reilly, M, Mortiboys, H, Prevo, R, Campanella, M, Daniels, M, Zeviani, M, Yu-Wai-Man, P, Simon, A, Votruba, M, Poulton, J

Real-world clinical experience with idebenone in the treatment of Leber hereditary optic neuropathy by Catarino, CB, von Livonius, B, Priglinger, C, Banik, R, Matloob, S, Tamhankar, MA, Castillo, L, Friedburg, C, Halfpenny, CA, Lincoln, JA, Traber, GL, Acaroglu, G, Black, GCM, Doncel, C, Fraser, CL, Jakubaszko, J, Landau, K, Langenegger, SJ, Muñoz-Negrete, FJ, Newman, NJ, Poulton, J, Scoppettuolo, E, Subramanian, P, Toosy, AT, Vidal, M, Vincent, AL, Votruba, M, Zarowski, M, Zermansky, A, Lob, F, Rudolph, G, Mikazans, O, Silva, M, Llòria, X, Metz, G, Klopstock, T