Foto del docente

Valerio Carelli

Professore associato

Dipartimento di Scienze Biomediche e Neuromotorie

Settore scientifico disciplinare: MED/26 NEUROLOGIA

Pubblicazioni

Ventura D.F.; Gualtieri M.; Oliveira A.G.; Costa M.F.; Quiros P.; Sadun F.; de Negri A.M.; Salomao S.R.; Berezovsky A.; Sherman J.; Sadun A.A.; Carelli V., Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy., «INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE», 2007, 48, pp. 2362 - 2370 [articolo]

Zeviani M.; Carelli V., Mitochondrial disorders., «CURRENT OPINION IN NEUROLOGY», 2007, 20, pp. 564 - 571 [articolo]

Carelli V.; La Morgia C.; Iommarini L.; Carroccia R.; Mattiazzi M.; Sangiorgi S.; Farné S.; Maresca A.; Foscarini B.; Lanzi L.; Amadori M.; Bellan M.; Valentino M.L., Mitochondrial optic neuropathies: how two genomes may kill the same cell type?, «BIOSCIENCE REPORTS», 2007, 27, pp. 173 - 184 [articolo]

S. Vidoni; C. Zanna; A. Ghelli; A.M. Porcelli; V. Carelli; M. Rugolo, OPA1 directly interacts with respiratory complexes and AIF., in: Frontiers in mitochondrial research: from bioenergetics to dynamycs, BERTINORO, University residential centre, 2007, pp. 125 - 125 (atti di: Frontiers in mitochondrial research: from bioenergetics to dynamycs, Bertinoro,, 25-28.11.2007) [atti di convegno-abstract]

G. Rizzo; V.Carelli; F. Fortuna; M.L. Valentino; D.N. Manners; C. Tonon; B. Barbiroli; R. Liguori; R. Lodi., Optic radiation impairment in Friedreich ataxia: a diffusion-weighted imaging and neurophysiological study., in: , «NEUROLOGICAL SCIENCES», 2007, 38, pp. 374 - 374 (atti di: XXXVIII Congress of the Italian Neurological Society, Firenze, 13-17 ottobre 2007) [atti di convegno-abstract]

C. Zanna; A. Ghelli; A.M. Porcelli ; S. Vidoni; V. Carelli; M. Rugolo:, Oxidative phosphorylation dysfunction in fibroblasts bearing different pathological OPA1 mutations., in: Frontiers in mitochondrial research: from bioenergetics to dynamics., BERTINORO, s.n, 2007, pp. 124 - 124 (atti di: Frontiers in mitochondrial research: from bioenergetics to dynamics., Bertinoro, 25-28.11.2007) [atti di convegno-abstract]

Coordinamento del progetto: Pathogenic mechanisms for degeneration of retinal ganglion cells in mitochondrial optic neuropathies (Prog. Telethon n. GGP06233).

C. La Morgia; A. Achilli; L. Iommarini; M. L. Valentino; P. Barboni; M. Pala; A. Olivieri; C. Tonon; R. Lodi; R. Vetrugno; B. Mostacci; R. Liguori; R. Carroccia; M. Amadori; P. Montagna; A. Torroni; V. Carelli, Rare mtDNA Variants in Leber's Hereditary Optic Neuropathy Families with Recurrence of Myoclonus, in: Neurology A1-A508, s.l, s.n, 2007, 68, pp. A40 - A40 (atti di: 59th American Academy of Neurology Annual Meeting, Boston, USA, April 28-May 5 2007) [atti di convegno-abstract]

Valentino M.L.; Martì R.; Tadesse S.; Lòpez L.C.; Manes J.L.; Lyzak J.; Hahn A.; Carelli V.; Hirano M., Thymidine and deoxyuridine accumulate in tissues of patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)., «FEBS LETTERS», 2007, 581, pp. 3410 - 3414 [articolo]

Hudson G.; Carelli V.; Horvath R.; Zeviani M.; Smeets H.J.; Chinnery P.F., X-inactivation patterns in females harboring mtDNA mutations that cause Leber hereditary optic neuropathy., «MOLECULAR VISION», 2007, 13, pp. 2339 - 2343 [articolo]

Bellan M.; Avoni P.; Liguori R.; Carroccia R.; Valentino M.L.; Villanova M.; La Morgia C.; Fulitano D.; Baruzzi A.; Lodi R.; Tonon C.; Lamantea E.; Zeviani M.; Carelli V., A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations., in: , «NEUROLOGICAL SCIENCES», 2006, 27, pp. S228 - S228 (atti di: XXXVII Congress of the Italian Neurological Society, Bari, 14-18 ottobre 2006) [atti di convegno-abstract]

Pizza F.; Donadio V.; Avoni P.; Panza E.; Sangiorgi S.; Seri M.; Carelli V.; Montagna P.; Liguori R., Autosomal dominant adult spinal muscular atrophy associated with alacrimia and achalasia., in: , «NEUROLOGICAL SCIENCES», 2006, 27, pp. S156 - S156 (atti di: XXXVII Congress of the Italian Neurological Society, Bari, 14-18 ottobre 2006) [atti di convegno-abstract]

Quiros P.A.; Torres R.J.; Salomao S.; Berezovsky A.; Carelli V.; Sherman J.; Sadun F.; De Negri A.; Belfort R.; Sadun A.A., Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study., «BRITISH JOURNAL OF OPHTHALMOLOGY», 2006, 90, pp. 150 - 153 [articolo]

Sgarbi G.; Baracca A.; Mattiazzi M.; Carelli V.; Lenaz G.; Solaini G., Comparative bioenergetic studies of cells carrying the 8993T>G or 8993T>C mitochondrial DNA mutations., in: Abstracts GIBB 2006, s.l, s.n, 2006, pp. 33 - 33 (atti di: Riunione Annuale del Gruppo Italiano di Bioenergetica e Biomembrane, Bertinoro, Italy, 15-17 June 2006) [atti di convegno-abstract]

A. M. Ghelli; C. Zanna; V. Carelli; A. Martinuzzi; M. Rugolo, Cybrids with mtDNA mutations causing Leber’s hereditary optic neuropathy are sensitized to apoptotic death induced by a mitochondrial oxidative stress, in: 14th Euroconference on Apoptosis "Death or survival? Fate in Sardinia", CHIA, s.n, 2006, pp. 200 - 200 (atti di: 14th Euroconference on Apoptosis "Death or survival? Fate in Sardinia", Chia, September 29 - October 4, 2006) [atti di convegno-abstract]