Foto del docente

Valerio Carelli

Full Professor

Department of Biomedical and Neuromotor Sciences

Academic discipline: MED/03 Medical Genetics

Publications

R. Lodi; C. Tonon; S. Iotti; V. Clementi; E. Malucelli; M. Valentino; P. Barboni; L. Longanesi; B. Wissinger; V. Carelli; B. Barbiroli, Deficit of in vivo mitochondrial ATP production in patients with OPA1-related autosomal dominant optic atrophy. A 31P-MRS study of the skeletal muscle., in: Proceedings of the International Society of Magnetic Resonance in Medicine (12th scientific meeting), s.l, ISMRM, 2004, pp. 2596 - 2596 (atti di: International Society for Magnetic Resonance in Medicine. 12th Scientific Meeting and Exhibition., Japan, 15-21 Maggio 2004) [Abstract]

Beretta S.; Mattavelli L.; Sala G.; Tremolizzo L.; Schapira A.H.; Martinuzzi A.; Carelli V.; Ferrarese C., Leber hereditary optic neuropathy mtDNA mutations disrupt glutamate transport in cybrid cell lines., «BRAIN», 2004, 127, pp. 2183 - 2192 [Scientific article]

Carelli V.; Ross-Cisneros F.N.; Sadun A.A., Mitochondrial dysfunction as a cause of optic neuropathies, «PROGRESS IN RETINAL AND EYE RESEARCH», 2004, 23, pp. 53 - 89 [Scientific article]

BARBONI P; SAVINI G; PLAZZI G.; BELLAN M; VALENTINO ML; ZANINI M; MONTAGNA P; HIRANO M; CARELLI V., Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report., «GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY», 2004, 242, pp. 878 - 880 [Scientific article]

Sadun F.; De Negri A.M.; Carelli V.; Salomao S.R.; Berezovsky A.; Andrade R.; Moraes M.; Passos A.; Belfort R.; Bastos Da Rosa A.; Quiros P.; Sadun A.A., Ophthalmologic findings in a large pedigree of 11778/Haplogroup J Leber hereditary optic neuropathy., «AMERICAN JOURNAL OF OPHTHALMOLOGY», 2004, 137, pp. 271 - 277 [Scientific article]

MANCUSO M; FILOSTO M; BELLAN M; LIGUORI R; MONTAGNA P; BARUZZI A.; DIMAURO S; CARELLI V., POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness., «NEUROLOGY», 2004, 62, pp. 316 - 318 [Scientific article]

Carelli V.; Ghelli A.; Baracca A.; Zanna C.; Sgarbi G.; Solaini G.; Lenaz G.; Rugolo M.; Martinuzzi A., Severe defect of complex I-dependent ATP synthesis shapes the mitochondria-driven path of apoptotic cell death in Leber’s Hereditary Optic Neuropathy., in: , «BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS», 2004, 1657, pp. 70 - 70 (atti di: Euromit 6-, Nijmegen, The Netherlands, 1-4 July 2004) [Abstract]

Achilli A.; Rengo C.; Magri C.; Battaglia V.; Olivieri A.; Scozzari R.; Cruciani F.; Zeviani M.; Briem M.; Carelli V.; Moral P.; Dugoujon J.M.; Roostalu U.; Loogvali E.L.; Kivisild T.; Bandelt H.J.; Richards M.; Villems R.; Santachiara-Benerecetti A.S.; Semino O.; Torroni A., The Molecular Dissection of mtDNA Haplogroup H Confirms That the Franco-Cantabrian Glacial Refuge Was a Major Source for the European Gene Pool., «AMERICAN JOURNAL OF HUMAN GENETICS», 2004, 75, pp. 910 - 918 [Scientific article]

VALENTINO ML; BARBONI P; GHELLI A; BUCCHI L; RENGO C; ACHILLI A; TORRONI A; LUGARESI A; LODI R; BARBIROLI B; DOTTI M; FEDERICO A; BARUZZI A.; CARELLI V., The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy., «ANNALS OF NEUROLOGY», 2004, 56, pp. 631 - 641 [Scientific article]

Salomao S.R.; Berezovsky A.; Andrade R.E.; Belfort R.; Carelli V.; Sadun A.A., Visual electrophysiologic findings in patients from an extensive Brazilian family with Leber's hereditary optic neuropathy., «DOCUMENTA OPHTHALMOLOGICA», 2004, 108, pp. 147 - 155 [Scientific article]