Showing 1 - 3 results of 3 for search 'Moroni, I', query time: 0.02s
Refine Results
-
1
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
Published 2012Conference item -
2
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
Published 2016Journal article -
3
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective? by Mastantuono, E, Repp, B, Alston, CL, Schiff, M, Haack, TB, Rotig, A, Ardissone, A, Lombes, A, Catarino, CB, Diodato, D, Schottmann, G, Poulton, J, Burlina, A, Jonckheere, A, Munnich, A, Ghezzi, D, Rokicki, D, Wellesley, D, Martinelli, D, Lamantea, E, Ostergaard, E, Pronicka, E, Pierre, G, Smeets, HJ, Scurr, I, De Coo, IF, Moroni, I, Smet, J, Mayr, JA, De Meirleir, L, Schuelke, M, Zeviani, M, McFarland, R, Seneca, S, Klopstock, T, Meitinger, T, Strom, TM, Herberg, U, Sperl, W, Nassogne, M, Ling, H, Fang, F, Freisinger, P, Van Coster, R, Taylor, RW, Haberle, J, Vockley, J, Prokisch, H, Wortmann, S
Published 2019Conference item