Authors:
Carelli, V
Valentino, ML
Liguori, R
Meletti, S
Vetrugno, R
Provini, F
Mancardi, GL
Bandini, F
Baruzzi, A
Montagna, P
Citation: V. Carelli et al., Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report oftwo cases, J NE NE PSY, 71(6), 2001, pp. 813-816
Authors:
Carelli, V
Di Colo, G
Nannipieri, E
Poli, B
Serafini, MF
Citation: V. Carelli et al., Polyoxyethylene-poly(methacrylic acid-co-methyl methacrylate) compounds for site-specific peroral delivery, INT J PHARM, 202(1-2), 2000, pp. 103-112
Authors:
Avoni, P
Monari, L
Carelli, V
Carcangiu, R
Barboni, P
Donati, C
Badiali, L
Baruzzi, A
Montagna, P
Citation: P. Avoni et al., Congenital encephalomyopathy with epilepsy, chorioretinitis, basal gangliainvolvement, and muscle minicores, ANN NEUROL, 47(3), 2000, pp. 395-399
Authors:
Carelli, V
Liberatore, F
Scipione, L
Musio, R
Sciacovelli, O
Citation: V. Carelli et al., On the structure of intermediate adducts arising from dithionite reductionof pyridinium salts: a novel class of derivatives of the parent sulfinic acid, TETRAHEDR L, 41(8), 2000, pp. 1235-1240
Authors:
Baracca, A
Barogi, S
Carelli, V
Lenaz, G
Solaini, G
Citation: A. Baracca et al., Catalytic activities of mitochondrial ATP synthase in patients with mitochondrial DNA T8993G mutation in the ATPase 6 gene encoding subunit alpha, J BIOL CHEM, 275(6), 2000, pp. 4177-4182
Authors:
Lodi, R
Montagna, P
Cortelli, P
Iotti, S
Cevoli, S
Carelli, V
Barbiroli, B
Citation: R. Lodi et al., 'Secondary' 4216/ND1 and 13708/ND5 Leber's hereditary optic neuropathy mitochondrial DNA mutations do not further impair in vivo mitochondrial oxidative metabolism when associated with the 11778/ND4 mitochondrial DNA mutation, BRAIN, 123, 2000, pp. 1896-1902
Authors:
Carelli, V
Ghelli, A
Bucchi, L
Montagna, P
De Negri, A
Leuzzi, V
Carducci, C
Lenaz, G
Lugaresi, E
Degli Esposti, M
Citation: V. Carelli et al., Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy, ANN NEUROL, 45(3), 1999, pp. 320-328