Cevoli S.; Pallotti F.; La Morgia C.; Valentino M.L.; Pierangeli G.; Cortelli P.; Baruzzi A.; Montagna P.; Carelli V., High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families., «CEPHALALGIA», 2010, 30, pp. 919 - 927 [Scientific article]
Yu-Wai-Man P;Griffiths PG;Gorman GS;Lourenco CM;Wright AF;Auer-Grumbach M;Toscano A;Musumeci O;Valentino ML;Caporali L;Lamperti C;Tallaksen CM;Duffey P;Miller J;Whittaker RG;Baker MR;Jackson MJ;Clarke MP;Dhillon B;Czermin B;Stewart JD;Hudson G;Reynier P;Bonneau D;Marques W Jr;Lenaers G;McFarland R;Taylor RW;Turnbull DM;Votruba M;Zeviani M;Carelli V;Bindoff LA;Horvath R;Amati-Bonneau P;Chinnery PF, Multi-system neurological disease is common in patients with OPA1 mutations., «BRAIN», 2010, 133, pp. 771 - 786 [Scientific article]
Barboni P.; Carbonelli M.; Savini G.; Foscarini B.; Parisi V.; Valentino M.L.; Carta A.; De Negri A.; Sadun F.; Zeviani M.; Sadun A.A.; Schimpf S.; Wissinger B.; Carelli V., OPA1 mutations associated with dominant optic atrophy influence optic nerve head size., «OPHTHALMOLOGY», 2010, 117, pp. 1547 - 1553 [Scientific article]
Vetrugno R.; Valentino M.L.; La Morgia C.; Liguori R.; Stecchi S.; Mascalchi M.; Fabbri M.; Montagna P.; Carelli V., Sleep-related periodic respiration with central sleep apnea in Leber Hereditary Optic Neuropathy (LHON)., «SLEEP MEDICINE», 2010, 11, pp. 426 - 427 [Scientific article]
do V.F. Ramos .C.; Bellusci C.; Savini G.; Carbonelli M.; Berezovsky A.; Tamaki C.; Cinoto R.; Sacai P.Y.; Moraes-Filho M.N.; Miura H.M.; Valentino M.L.; Iommarini L.; De Negri A.M.; Sadun F.; Cortelli P.; Montagna P.; Salomao S.R.; Sadun A.A.; Carelli V.; Barboni P., Association of optic disc size with development and prognosis of Leber's hereditary optic neuropathy., «INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE», 2009, 50, pp. 1666 - 1674 [Scientific article]
Carelli V.; La Morgia C.; Valentino M.L.; Barboni P.; Ross-Cisneros F.N.; Sadun A.A., Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders., «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2009, 1787, pp. 518 - 528 [Scientific article]
Fortuna, F.; Barboni, P.; Liguori, R.; Valentino, M.L.; Savini, G.; Gellera, C.; Mariotti, C.; Rizzo, G.; Tonon, C.; Manners, D.; Lodi, R.; Sadun, A.A.; Carelli, V., Visual system involvement in patients with Friedreich's ataxia, «BRAIN», 2009, 132, pp. 116 - 123 [Scientific article]
D'Aguanno S.; Barassi A.; Lupisella S.; d'eril G.M.; Del Boccio P.; Pieragostino D.; Pallotti F.; Carelli V.; Valentino M.L.; Liguori R.; Avoni P.; Bernardini S.; Gambi D.; Urbani A.; Federici G., Differential cerebro spinal fluid proteome investigation of Leber hereditary optic neuropathy (LHON) and multiple sclerosis., «JOURNAL OF NEUROIMMUNOLOGY», 2008, 193, pp. 156 - 160 [Scientific article]
Shankar S.P.; Fingert J.H.; Carelli V.; Valentino M.L.; King T.M.; Daiger S.P.; Salomao S.R.; Berezovsky A.; Belfort R. Jr.; Braun T.A.; Sheffield V.C.; Sadun A.A.; Stone E.M., Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy., «OPHTHALMIC GENETICS», 2008, 29, pp. 17 - 24 [Scientific article]
Giordano C; Sebastiani M; De Giorgio R; Travaglini C; Tancredi A; Valentino ML; Bellan M; Cossarizza A; Hirano M; d'Amati G; Carelli V., Gastrointestinal dysmotility in mitochondrial neurogastrointestinal encephalomyopathy is caused by mitochondrial DNA depletion., «THE AMERICAN JOURNAL OF PATHOLOGY», 2008, 173, pp. 1120 - 1128 [Scientific article]
Zanna C.; Ghelli A.; Porcelli A.M.; Karbowski M.; Youle R.J.; Schimpf S.; Wissinger B.; Pinti M.; Cossarizza A.; Vidoni S.; Valentino M.L.; Rugolo M.; Carelli V., OPA 1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion., «BRAIN», 2008, 131, pp. 352 - 367 [Scientific article]
Amati-Bonneau P.; Valentino M.L.; Reynier P.; Gallardo M.E.; Bornstein B.; Boissiere A.; Campos Y; Rivera H; de la Aleja J.G.; Carroccia R.; Iommarini L.; Labauge P.; Figarella-Branger D.; Marcorelles P.; Furby A.; Beauvais K.; Letournel F.; Liguori R.; La Morgia C.; Montagna P.; Liguori M.; Zanna C.; Rugolo M.; Cossarizza A.; Wissinger B.; Verny C.; Schwarzenbacher R.; Martin M.A.; Arenas J.; Ayuso C.; Garesse R.; Lenaers G.; Bonneau D.; Carelli V., OPA 1 mutations induce mitochondrial DNA instability and optic atrophy "plus" phenotypes, «BRAIN», 2008, 131, pp. 338 - 351 [Scientific article]
Carelli, V; Reynier, P; Lucia, M; Labauge, P; Verny, C; Furby, A; Lenaers, G; Carroccia, R; Iommarini, L; La Morgia, C; Liguori, R; Zanna, C; Campos, Y; Arenas, J; Garesse, R; Wissinger, B; Bonneau, D; Amati-Bonneau, P, OPA1 mutations induce mitochondrial DNA instability and optic atrophy plus phenotypes, in: 60th Annual Meeting of the American-Academy-of-Neurology, TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA, LIPPINCOTT WILLIAMS & WILKINS, «NEUROLOGY», 2008, 70, pp. A486 - A486 (atti di: 60th Annual Meeting of the American-Academy-of-Neurology, Chicago, 12-19 Aprile 2008) [Abstract]
Genasetti A.; Valentino M.L.; Carelli V.; Vigetti D.; Viola M.; Karousou E.G.; Melzi d'Eril G.V.; De Luca G.; Passi A.; Pallotti F., Assessing heteroplasmic load in Leber's hereditary optic neuropathy mutation 3460G->A/MT-ND1 with a real-time PCR quantitative approach., «THE JOURNAL OF MOLECULAR DIAGNOSTICS», 2007, 9, pp. 538 - 545 [Scientific article]
Baracca A; Sgarbi G; Mattiazzi M; Casalena G; Pagnotta E; Valentino ML; Moggio M; Lenaz G; Carelli V; Solaini G., Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2007, 1767, pp. 913 - 919 [Scientific article]
