Foto del docente

Valerio Carelli

Full Professor

Department of Biomedical and Neuromotor Sciences

Academic discipline: MED/03 Medical Genetics

Publications

BONORA E.; PORCELLI A.M.; GASPARRE G.; BIONDI A.; GHELLI A.; CARELLI V.; BARACCA A.; TALLINI G.; MARTINUZZI A.; LENAZ G.; RUGOLO M.; ROMEO G., Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III, «CANCER RESEARCH», 2006, 66, pp. 6087 - 6096 [Scientific article]

Savini G.; Bellusci C.; Carbonelli M.; Zanini M.; Carelli V.; Sadun A.A.; Barboni P., Detection and quantification of retinal nerve fiber layer thickness in optic disc edema using stratus OCT., «ARCHIVES OF OPHTHALMOLOGY», 2006, 124, pp. 1111 - 1117 [Scientific article]

C. Zanna; A. Ghelli; A. M.Porcelli; M. Karbowski; R.J. Youle; V. Carelli; M. Rugolo, Determination of mitochondrial fusion in fibroblasts from dominant optic atrophy patients bearing the c.2708delttag OPA1 mutation, in: Riunione Annuale del GRUPPO ITALIANO DI BIOMEMBRANE E BIOENERGETICA, s.l, s. n., 2006, pp. 31 - 31 (atti di: Riunione Annuale del GRUPPO ITALIANO DI BIOMEMBRANE E BIOENERGETICA, GIBB 2006, Bertinoro (FO), 15-17 Giugno 2006) [Abstract]

La Morgia C.; Valentino M.L.; Barboni P.; Bellan M.; Carroccia R.; Liguori R.; Avoni P.; Cortelli P.; Montagna P.; Baruzzi A.; Carelli V., Extraocular Clinical Features in Leber's Hereditary Optic Neuropathy (LHON) Italian Families., in: , «NEUROLOGY», 2006, 66(suppl. 2), pp. A20 - A21 (atti di: American Academy of Neurology, Annual Meeting, San Diego, CA, USA, April 1-8, 2006) [Abstract]

Carelli V.; Achilli A.; Valentino M.L.; Rengo C.; Semino O.; Pala M.; Olivieri A.; Mattiazzi M.; Pallotti F.; Carrara F.; Zeviani M.; Leuzzi V.; Carducci C.; Valle G.; Simionati B.; Mendieta L.; Salomao S.; Belfort R. Jr.; Sadun A.A.; Torroni A., Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees., «AMERICAN JOURNAL OF HUMAN GENETICS», 2006, 78, pp. 564 - 574 [Scientific article]

M. Rugolo; C. Zanna; A. Ghelli; R. J. Youle; V. Carelli, Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration, in: The Italian Journal of Biochemistry, s.l, s.n, 2006, 55, pp. 109 - 109 (atti di: SIB 2006, Riccione, 28 - 30 September 2006) [Abstract]

Sanchez R.N.; Smith A.J.; Carelli V.; Sadun A.A.; Keltner J.L., Leber hereditary optic neuropathy possibly triggered by exposure to tire fire., «JOURNAL OF NEURO-OPHTHALMOLOGY», 2006, 26, pp. 268 - 272 [Scientific article]

Barboni P.; Savini G.; Valentino M.L.; La Morgia C.; Bellusci C.; De Negri A.M.; Sadun F.; Carta A.; Carbonelli M.; Sadun A.A.; Carelli V., Leber's Hereditary Optic Neuropathy with childhood onset., «INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE», 2006, 47, pp. 5303 - 5309 [Scientific article]

Cortopassi G; Danielson S.; Alemi M.; Zhan S.S.; Tong W.; Carelli V.; Martinuzzi A.; Marzuki S.; Majamaa K.; Wong A., Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts., «MITOCHONDRION», 2006, 6, pp. 161 - 175 [Scientific article]

Giordano C.; Sebastiani M.; Plazzi G.; Travaglini C.; Sale P.; Pinti M.; Tancredi A.; Liguori R.; Montagna P.; Bellan M.; Valentino M.L.; Cossarizza A.; Hirano M.; d'Amati G.; Carelli V., Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine., «GASTROENTEROLOGY», 2006, 130, pp. 893 - 901 [Scientific article]

Bellan M.; La Morgia C.; Liguori R.; Villanova M.; Carroccia R.; Avoni P.; Lodi R.; Tonon C.; Baruzzi A.; Carelli V., Myopathy and retinopathy are novel features in a patient with Mohr-Tranebjaerg syndrome., in: , «NEUROLOGICAL SCIENCES», 2006, 27, pp. S233 - S234 (atti di: XXXVII Congress of the Italian Neurological Society, Bari, 14-18 ottobre 2006) [Abstract]

Carelli V.; Schimpf S.; Valentino M.L.; Barboni P.; De Negri A.M.; Sadun F.; La Morgia C.; Bellan M.; Amadori M.; Schaich S.; Wissinger B., OPA1 Gene Screening in Italian Dominant Optic Neuropathy (DOA) Patients Reveals New Mutations and Genetic Heterogeneity., in: , «NEUROLOGY», 2006, 66(suppl. 2), pp. A21 - A21 (atti di: American Academy of Neurology, Annual Meeting, San Diego, CA, USA, April 1-8, 2006) [Abstract]

R. Lodi; C. Tonon; D. Manners; E. Malucelli; C. Testa; M.L. Valentino; P. Barboni; S. Schaich; S. Schimpf; B. Wissinger; V. Carelli; B. Barbiroli, OPA1 Mutations Result in a Deficit of In Vivo Mitochondrial ATP Production in Patients with Autosomal Dominant Optic Atrophy, in: ISMRM Fourteenth Scientific Meeting and Exhibition, s.l, s.n, 2006, pp. 338 - 338 (atti di: ISMRM Fourteenth Scientific Meeting and Exhibition, Seattle, Washington, USA, 6-12 Maggio 2006) [Abstract]

Savini G.; Zanini M.; Carelli V.; Sadun A.A.; Ross-Cisneros F.N.; Barboni P., Optic nerve structure in healthy subjects., «ARCHIVES OF OPHTHALMOLOGY», 2006, 124, pp. 1507 - 1507 [Scientific article]

Beretta S.; Ferrarese C.; Wood J.P.; Osborne N.N.; Carelli V., Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate., «MITOCHONDRION», 2006, 6, pp. 102 - 103 [Scientific article]