Ghelli A.; Tropeano C.V.; Calvaruso M.A.; Marchesini A.; Iommarini L.; Porcelli A.M.; Zanna C.; Gasparre G.; Kurelac I.; De Nardo V.; Martinuzzi A.; Vissing J.; Selamoglu N.; Daldal F.; Rugolo M., Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder, in: BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2012, 1817, pp. S139 - S139 (atti di: EBEC 2012 - 17th European Bioenergetics Conference, Freiburg, 15-20 September 2012) [Abstract]
Achilli A.; Iommarini L.; Olivieri A.; Pala M.; Hooshiar Kashani B.; Reynier P.; La Morgia C.; Valentino M.L.; Liguori R.; Pizza F.; Barboni P.; Sadun F.; De Negri A.M.; Zeviani M.; Dollfus H.; Moulignier A.; Ducos G.; Orssaud C.; Bonneau D.; Procaccio V.; Leo-Kottler B.; Fauser S.; Wissinger B.; Amati-Bonneau P.; Torroni A.; Carelli V., Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy., «PLOS ONE», 2012, 7, Article number: e42242 , pp. 1 - 11 [Scientific article]Open Access
Iommarini L.; Maresca A.; Caporali L.; Valentino M.L.; Liguori R.; Giordano C.; Carelli V., Revisiting the issue of mitochondrial DNA content in optic
mitochondriopathies, «NEUROLOGY», 2012, 79, pp. 1517 - 1519 [Scientific article]
Leonardo Caporali;Carla Giordano;Luisa Iommarini;Alessandra Maresca;Pio D'adamo;Solange R. Salomao;Rubens Belfort;Alfredo Sadun;Valerio Carelli, Searching for genetic modifiers of Leber's hereditary optic neuropathy penetrance, «MITOCHONDRION», 2012, 12, pp. 572 - 572 [Abstract]
Carelli V.; Schimpf S.; Fuhrmann N.; Valentino M.L.; Zanna C.; Iommarini L.; Papke M.; Schaich S.; Tippmann S.; Baumann B.; Barboni P.; Longanesi L.; Rugolo M.; Ghelli A.; Alavi M.V.; Youle R.J.; Bucchi L.; Carroccia R.; Giannoccaro M.P.; Tonon C.; Lodi R.; Cenacchi G.; Montagna P.; Liguori R.; Wissinger B., A clinically complex form of dominant optic atrophy (OPA8) maps on chromosome 16., «HUMAN MOLECULAR GENETICS», 2011, 20, pp. 1893 - 1905 [Scientific article]
Gasparre G; Kurelac I; Capristo M; Iommarini L; Ghelli A; Ceccarelli C; Nicoletti G; Nanni P; De Giovanni C; Scotlandi K; Betts CM; Carelli V; Lollini PL; Romeo G; Rugolo M; Porcelli AM, A Mutation Threshold Distinguishes the Antitumorigenic Effects of the Mitochondrial Gene MTND1, an Oncojanus Function, «CANCER RESEARCH», 2011, 71, pp. 6220 - 6229 [Scientific article]
Gonzalez-Halphen D; Ghelli A; Iommarini L; Carelli V; Degli Esposti M, Mitochondrial complex I and cell death: a semi-automatic shogun model, «CELL DEATH & DISEASE», 2011, 2, Article number: e222 , pp. 1 - 7 [Scientific article]Open Access
G.Gasparre; L. Iommarini; A.M. Porcelli; M. Lang; G.G. Ferri; I.Kurelac; E. Mariani; L.F. Pennisi; E. Pasquini; G. Pasquinelli; A. Ghelli; E. Bonora; C. Ceccarelli; M. Rugolo; N. Salfi; G. Romeo; V. Carelli., An inherited mitochondrial DNA disruptive mutation shifts to homoplasmy in oncocytic tumor cells., «HUMAN MUTATION», 2009, 30 (3), pp. 391 - 396 [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]
Iommarini L.; Martelli P.L.; Ghelli A.; Rugolo M.; Casadio R.; Carelli V., Modelling ND subunits of complex I: Leber’s Hereditary Optic Neuropathy (LHON) pathogenic mutations and non-synonymous population variants in genotype-phenotype correlation, in: Proceedings of Mitochondial Medicine 2009, s.l, s.n, 2009, pp. 194 - 195 (atti di: Mitochondial Medicine 2009, Vienna, Virginia, USA, 24-27 Giugno 2009) [Abstract]
Srivastava S;Diaz F;Iommarini L;Aure K;Lombes A;Moraes CT, PGC-1alpha/beta induced expression partially compensates for respiratory chain defects in cells from patients with mitochondrial disorders., «HUMAN MOLECULAR GENETICS», 2009, 18, pp. 1805 - 1812 [Scientific article]
Ghelli A.; Porcelli A.M.; Zanna C.; Vidoni S.; Mattioli S.; Barbieri A.; Iommarini L.; Pala M.; Achilli A.; Torroni A.; Rugolo M.; Carelli V., The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity., «PLOS ONE», 2009, 4, Article number: e7922 , pp. 1 - 11 [Scientific article]Open Access
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]
La Morgia C.; Achilli A.; Iommarini L.; Barboni P.; Pala M.; Olivieri A.; Zanna C.; Vidoni S.; Tonon C.; Lodi R.; Vetrugno R.; Mostacci B.; Liguori R.; Carroccia R;. Montagna P.; Rugolo M.; Torroni A.; Carelli V., Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus., «NEUROLOGY», 2008, 70, pp. 762 - 770 [Scientific article]