Sfoglia per Autore
Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy.
2005 Floreani M.; Napoli E.; Martinuzzi A.; Pantano G.; De Riva V.; Trevisan R.; Bisetto E.; Valente L.; Carelli V.; Dabbeni-Sala F.
Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA).
2005 C. Zanna; A. Ghelli; A. M. Porcelli; V. Carelli; M. Rugolo
Severe impairment of Complex I-driven adenosine triphosphate synthesis in leber hereditarfy optic neuropathy cybrids
2005 Baracca A.; Solaini G.; Sgarbi G.; Lenaz G.; Baruzzi A.; Schapira A.H.; Martinuzzi A.; Carelli V.
Dominance in mitochondrial disorders.
2005 Zeviani M.; Carelli V.
Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathy.
2005 Bose S.; Dhillon N.; Ross-Cisneros F.N.; Carelli V.
Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies.
2005 A. Ghelli; C. Zanna; S. Cumero; A.M. Porcelli; V. Carelli; M. Rugolo
Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations.
2005 Savini G.; Barboni P.; Valentino M.L.; Montagna P.; Cortelli P.; De Negri A.M.; Sadun F.; Bianchi S.; Longanesi L.; Zanini M.; Carelli V.
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy.
2005 ventura D.F.; Quiros P.; Carelli V.; Salomao S.R.; Gualtieri M.; Oliveira A.G.; Costa M.F.; Berezovsky A.; Sadun F.; de Negri A.M.; Sadun A.A.
Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy.
2005 Carta A.; Carelli V.; D'Adda T.; Ross-Cisneros F.N.; Sadun A.A.
Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study.
2006 Sadun A.A.; Salomao S.R.; Berezovsky A.; Sadun F.; Denegri A.M.; Quiros P.A.; Chicani F.; Ventura D.; Barboni P.; Sherman J.; Sutter E.; Belfort R. Jr; Carelli V.
Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine.
2006 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.
Leber hereditary optic neuropathy possibly triggered by exposure to tire fire.
2006 Sanchez R.N.; Smith A.J.; Carelli V.; Sadun A.A.; Keltner J.L.
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.
2006 Quiros P.A.; Torres R.J.; Salomao S.; Berezovsky A.; Carelli V.; Sherman J.; Sadun F.; De Negri A.; Belfort R.; Sadun A.A.
Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III
2006 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.
Detection and quantification of retinal nerve fiber layer thickness in optic disc edema using stratus OCT.
2006 Savini G.; Bellusci C.; Carbonelli M.; Zanini M.; Carelli V.; Sadun A.A.; Barboni P.
Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts.
2006 Cortopassi G; Danielson S.; Alemi M.; Zhan S.S.; Tong W.; Carelli V.; Martinuzzi A.; Marzuki S.; Majamaa K.; Wong A.
Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate.
2006 Beretta S.; Ferrarese C.; Wood J.P.; Osborne N.N.; Carelli V.
Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA
2006 Gianluca Sgarbi; Alessandra Baracca; Giorgio Lenaz; Lucia M. Valentino; Valerio Carelli; Giancarlo Solaini
Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration
2006 M. Rugolo; C. Zanna; A. Ghelli; R. J. Youle; V. Carelli
A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations.
2006 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.
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Antioxidant defences in cybrids harboring mtDNA mutations associated with Leber's hereditary optic neuropathy. | Floreani M.; Napoli E.; Martinuzzi A.; Pantano G.; De Riva V.; Trevisan R.; Bisetto E.; Valente L....; Carelli V.; Dabbeni-Sala F. | 2005-01-01 | THE FEBS JOURNAL | - | 1.01 Articolo in rivista | - |
| Evaluation of the energetic efficiency of cells derived from patients with dominant optic neuropathy (DOA). | C. Zanna; A. Ghelli; A. M. Porcelli; V. Carelli; M. Rugolo | 2005-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| Severe impairment of Complex I-driven adenosine triphosphate synthesis in leber hereditarfy optic neuropathy cybrids | Baracca A.; Solaini G.; Sgarbi G.; Lenaz G.; Baruzzi A.; Schapira A.H.; Martinuzzi A.; Carelli V. | 2005-01-01 | ARCHIVES OF NEUROLOGY | - | 1.01 Articolo in rivista | - |
| Dominance in mitochondrial disorders. | Zeviani M.; Carelli V. | 2005-01-01 | JOURNAL OF INHERITED METABOLIC DISEASE | - | 1.01 Articolo in rivista | - |
| Relative post-mortem sparing of afferent pupil fibers in a patient with 3460 Leber's hereditary optic neuropathy. | Bose S.; Dhillon N.; Ross-Cisneros F.N.; Carelli V. | 2005-01-01 | GRAEFE'S ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| Energetic efficiency and mitochondrial dynamics in fibroblasts derived from patients with optic neuropathies. | A. Ghelli; C. Zanna; S. Cumero; A.M. Porcelli; V. Carelli; M. Rugolo | 2005-01-01 | - | University of Bari | 4.02 Riassunto (Abstract) | - |
| Retinal nerve fiber layer evaluation by optical coherence tomography in unaffected carriers with Leber's hereditary optic neuropathy mutations. | Savini G.; Barboni P.; Valentino M.L.; Montagna P.; Cortelli P.; De Negri A.M.; Sadun F.; Bianchi... S.; Longanesi L.; Zanini M.; Carelli V. | 2005-01-01 | OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy. | ventura D.F.; Quiros P.; Carelli V.; Salomao S.R.; Gualtieri M.; Oliveira A.G.; Costa M.F.; Berez...ovsky A.; Sadun F.; de Negri A.M.; Sadun A.A. | 2005-01-01 | INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | - | 1.01 Articolo in rivista | - |
| Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy. | Carta A.; Carelli V.; D'Adda T.; Ross-Cisneros F.N.; Sadun A.A. | 2005-01-01 | BRITISH JOURNAL OF OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| Subclinical carriers and conversions in Leber hereditary optic neuropathy: a prospective psychophysical study. | Sadun A.A.; Salomao S.R.; Berezovsky A.; Sadun F.; Denegri A.M.; Quiros P.A.; Chicani F.; Ventura... D.; Barboni P.; Sherman J.; Sutter E.; Belfort R. Jr; Carelli V. | 2006-01-01 | TRANSACTIONS OF THE AMERICAN OPHTHALMOLOGICAL SOCIETY | - | 1.01 Articolo in rivista | - |
| Mitochondrial neurogastrointestinal encephalomyopathy: evidence of mitochondrial DNA depletion in the small intestine. | 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. | 2006-01-01 | GASTROENTEROLOGY | - | 1.01 Articolo in rivista | - |
| Leber hereditary optic neuropathy possibly triggered by exposure to tire fire. | Sanchez R.N.; Smith A.J.; Carelli V.; Sadun A.A.; Keltner J.L. | 2006-01-01 | JOURNAL OF NEURO-OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| 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. | Quiros P.A.; Torres R.J.; Salomao S.; Berezovsky A.; Carelli V.; Sherman J.; Sadun F.; De Negri A....; Belfort R.; Sadun A.A. | 2006-01-01 | BRITISH JOURNAL OF OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III | 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. | 2006-01-01 | CANCER RESEARCH | - | 1.01 Articolo in rivista | - |
| Detection and quantification of retinal nerve fiber layer thickness in optic disc edema using stratus OCT. | Savini G.; Bellusci C.; Carbonelli M.; Zanini M.; Carelli V.; Sadun A.A.; Barboni P. | 2006-01-01 | ARCHIVES OF OPHTHALMOLOGY | - | 1.01 Articolo in rivista | - |
| Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts. | Cortopassi G; Danielson S.; Alemi M.; Zhan S.S.; Tong W.; Carelli V.; Martinuzzi A.; Marzuki S.; ...Majamaa K.; Wong A. | 2006-01-01 | MITOCHONDRION | - | 1.01 Articolo in rivista | - |
| Pathogenesis of retinal ganglion cell death in Leber hereditary optic neuropathy (LHON): possible involvement of mitochondria, light and glutamate. | Beretta S.; Ferrarese C.; Wood J.P.; Osborne N.N.; Carelli V. | 2006-01-01 | MITOCHONDRION | - | 1.01 Articolo in rivista | - |
| Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA | Gianluca Sgarbi; Alessandra Baracca; Giorgio Lenaz; Lucia M. Valentino; Valerio Carelli; Giancarl...o Solaini | 2006-01-01 | BIOCHEMICAL JOURNAL | - | 1.01 Articolo in rivista | - |
| Impairment of mitochondrial fusion in dominant optic atrophy, a model for selective neurodegeneration | M. Rugolo; C. Zanna; A. Ghelli; R. J. Youle; V. Carelli | 2006-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
| A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations. | Bellan M.; Avoni P.; Liguori R.; Carroccia R.; Valentino M.L.; Villanova M.; La Morgia C.; Fulita...no D.; Baruzzi A.; Lodi R.; Tonon C.; Lamantea E.; Zeviani M.; Carelli V. | 2006-01-01 | NEUROLOGICAL SCIENCES | - | 4.02 Riassunto (Abstract) | - |
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