Sfoglia per Autore
Metabolic muscle adaptation to aerobic training in patients affected by mitochondrial myopathies.
2001-01-01 Siciliano, Gabriele; Tovani, S; Mancuso, Michelangelo; Pasquali, Livia; Rocchi, Anna; Manca, MARIA LAURA; Murri, Luigi
Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.
2001-01-01 Berrettini, Stefano; Forli, Francesca; Siciliano, Gabriele; Mancuso, Michelangelo
Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports
2001-01-01 Siciliano, Gabriele; Mancuso, Michelangelo; Ceravolo, Roberto; Lombardi, V; Iudice, Alfonso; Bonuccelli, Ubaldo
Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy
2001-01-01 Siciliano, Gabriele; Mancuso, Michelangelo; Tedeschi, D; Manca, MARIA LAURA; Renna, Mr; Lombardi, V; Rocchi, A; Martelli, Franco; Murri, Luigi
Proximal myotonic myopathy: report on italian families and literature review.
2001-01-01 Meola, G; Sansone, V; Vitelli, E; Mancuso, Michelangelo; Siciliano, Gabriele
Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion.
2001-01-01 Berrettini, S; Forli, F; Siciliano, Gabriele; Mancuso, Michelangelo
Assessment of endogenous DNA oxidative stress in mitochondrial encephalomyopathies.
2002-01-01 Mancuso, Michelangelo; Naccarati, A; Molinu, S; Del Corona, A; Tovani, S; Galluzzi, F; Pasquali, Livia; Migliore, Lucia; Siciliano, Gabriele
Peripheral benzodiazepine binding sites in platelets of patients affected by mitochondrial diseases and large scale mitochondrial DNA rearrangements
2002-01-01 Martini, Claudia; B., Chelli; Betti, Laura; M., Montali; Mancuso, Michelangelo; Giannaccini, Gino; A., Rocchi; L., Murri; Siciliano, Gabriele
A screening for superoxide dismutase-1 d90a mutation in italian patients with sporadic amyotrophic lateral sclerosis
2002-01-01 Mancuso, Michelangelo; Filosto, M; Naini, A; Rocchi, A; DEL CORONA, A; Sartucci, Ferdinando; Siciliano, Gabriele; Murri, L.
COX AND MITOCHONDRIAL F1F0-ATPASE (ATP SYNTHASE) ACTIVITIES IN PLATELETS AND BRAIN FROM PATIENTS WITH ALZHEIMER'S DISEASE
2002-01-01 Bosetti, F; Brizzi, F; Barogi, S; Mancuso, Michelangelo; Siciliano, Gabriele
Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in hashimoto's hypothyroid myopathy
2002-01-01 Siciliano, Gabriele; Monzani, Fabio; Manca, MARIA LAURA; Tessa, A; Caraccio, NADIA MARIA; Tozzi, G; Piemonte, F; Mancuso, Michelangelo; Santorelli, Fm; Ferrannini, Eleuterio; Murri, Luigi
dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism
2002-01-01 Orlandi, Giovanni; Fanucchi, S; Mancuso, Michelangelo; Gelli, A; Rocchi, A; Siciliano, Gabriele; Murri, Luigi
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2)
2003-01-01 Meola, G; Sansone, V; Perani, D; Scarone, S; Cappa, S; Dragoni, C; Cattaneo, E; Cotelli, M; Gobbo, C; Fazio, F; Siciliano, Gabriele; Mancuso, Michelangelo; Vitelli, E; Zhang, S; Krahe, R; Moxley, Rt
Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease
2003-01-01 Mancuso, Michelangelo; Filosto, M; Bosetti, F; Ceravolo, Roberto; Rocchi, Anna; Tognoni, G; Manca, MARIA LAURA; Solaini, G; Siciliano, Gabriele; Murri, Luigi
P301L TAU MUTATION AND NON-ALZHEIMER DEMENTIAS IN ITALY
2003-01-01 Mancuso, Michelangelo; Leone, M; Filosto, M; Tognoni, G; Siciliano, Gabriele; Nichelli, P; Murri, Luigi
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance
2003-01-01 Bianchi, M. C.; Tosetti, M.; Battini, R.; Manca, MARIA LAURA; Mancuso, Michelangelo; Cioni, Giovanni; Canapicchi, R.; Siciliano, Gabriele
Proton MR Spectroscopy of mitochondrial diseases: Analysis of brain metabolic abnormalities and their possible diagnostic relevance
2003-01-01 Bianchi, Mc; Tosetti, M; Battini, R; Mancuso, M; Cioni, G; Canapicchi, R and Siciliano G
AUTOSOMAL DOMINANT EXTERNAL OPHTHALMOPLEGIA AND BIPOLAR AFFECTIVE DISORDER ASSOCIATED WITH A MUTATION IN THE ANT1 GENE
2003-01-01 Siciliano, Gabriele; Tessa, A; Petrini, S; Mancuso, Michelangelo; Bruno, C; Grieco, Gs; Malandrini, A; Deflorio, L; Martini, B; Federico, A; Nappi, G; Santorelli, Fm; Murri, Luigi
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?
2004-01-01 Mancuso, Michelangelo; Murri, Luigi; Rocchi, A; Tessitore, A; Muglia, M; Tedeschi, G; Panza, D; Monsurr, Mr; Sola, P; Mandrioli, J; Choub, A; Delcorona, A; Manca, MARIA LAURA; Mazzei, Rl; Sprovieri, T; Filosto, M; Salviati, A; Valentino, P; Bono, F; Caracciolo, M; Simone, Il; LA BELLA, V; Majorana, G; Siciliano, Gabriele; Murri, L; Quattrone, A.
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome
2004-01-01 Mancuso, Michelangelo; Filosto, M; Mootha, Vk; Rocchi, A; Pistolesi, S; Murri, Luigi; Dimauro, S; Siciliano, Gabriele
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Metabolic muscle adaptation to aerobic training in patients affected by mitochondrial myopathies. | 1-gen-2001 | Siciliano, Gabriele; Tovani, S; Mancuso, Michelangelo; Pasquali, Livia; Rocchi, Anna; Manca, MARIA LAURA; Murri, Luigi | |
Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion. | 1-gen-2001 | Berrettini, Stefano; Forli, Francesca; Siciliano, Gabriele; Mancuso, Michelangelo | |
Mitochondrial DNA rearrangements in young onset parkinsonism: two case reports | 1-gen-2001 | Siciliano, Gabriele; Mancuso, Michelangelo; Ceravolo, Roberto; Lombardi, V; Iudice, Alfonso; Bonuccelli, Ubaldo | |
Coenzyme Q10, exercise lactate and CTG trinucleotide expansion in myotonic dystrophy | 1-gen-2001 | Siciliano, Gabriele; Mancuso, Michelangelo; Tedeschi, D; Manca, MARIA LAURA; Renna, Mr; Lombardi, V; Rocchi, A; Martelli, Franco; Murri, Luigi | |
Proximal myotonic myopathy: report on italian families and literature review. | 1-gen-2001 | Meola, G; Sansone, V; Vitelli, E; Mancuso, Michelangelo; Siciliano, Gabriele | |
Sudden bilateral hearing loss and sporadic mitochondrial DNA deletion. | 1-gen-2001 | Berrettini, S; Forli, F; Siciliano, Gabriele; Mancuso, Michelangelo | |
Assessment of endogenous DNA oxidative stress in mitochondrial encephalomyopathies. | 1-gen-2002 | Mancuso, Michelangelo; Naccarati, A; Molinu, S; Del Corona, A; Tovani, S; Galluzzi, F; Pasquali, Livia; Migliore, Lucia; Siciliano, Gabriele | |
Peripheral benzodiazepine binding sites in platelets of patients affected by mitochondrial diseases and large scale mitochondrial DNA rearrangements | 1-gen-2002 | Martini, Claudia; B., Chelli; Betti, Laura; M., Montali; Mancuso, Michelangelo; Giannaccini, Gino; A., Rocchi; L., Murri; Siciliano, Gabriele | |
A screening for superoxide dismutase-1 d90a mutation in italian patients with sporadic amyotrophic lateral sclerosis | 1-gen-2002 | Mancuso, Michelangelo; Filosto, M; Naini, A; Rocchi, A; DEL CORONA, A; Sartucci, Ferdinando; Siciliano, Gabriele; Murri, L. | |
COX AND MITOCHONDRIAL F1F0-ATPASE (ATP SYNTHASE) ACTIVITIES IN PLATELETS AND BRAIN FROM PATIENTS WITH ALZHEIMER'S DISEASE | 1-gen-2002 | Bosetti, F; Brizzi, F; Barogi, S; Mancuso, Michelangelo; Siciliano, Gabriele | |
Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in hashimoto's hypothyroid myopathy | 1-gen-2002 | Siciliano, Gabriele; Monzani, Fabio; Manca, MARIA LAURA; Tessa, A; Caraccio, NADIA MARIA; Tozzi, G; Piemonte, F; Mancuso, Michelangelo; Santorelli, Fm; Ferrannini, Eleuterio; Murri, Luigi | |
dissection and atherosclerosis of carotid arteries in the young: role of the apolipoprotein E polymorphism | 1-gen-2002 | Orlandi, Giovanni; Fanucchi, S; Mancuso, Michelangelo; Gelli, A; Rocchi, A; Siciliano, Gabriele; Murri, Luigi | |
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2) | 1-gen-2003 | Meola, G; Sansone, V; Perani, D; Scarone, S; Cappa, S; Dragoni, C; Cattaneo, E; Cotelli, M; Gobbo, C; Fazio, F; Siciliano, Gabriele; Mancuso, Michelangelo; Vitelli, E; Zhang, S; Krahe, R; Moxley, Rt | |
Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease | 1-gen-2003 | Mancuso, Michelangelo; Filosto, M; Bosetti, F; Ceravolo, Roberto; Rocchi, Anna; Tognoni, G; Manca, MARIA LAURA; Solaini, G; Siciliano, Gabriele; Murri, Luigi | |
P301L TAU MUTATION AND NON-ALZHEIMER DEMENTIAS IN ITALY | 1-gen-2003 | Mancuso, Michelangelo; Leone, M; Filosto, M; Tognoni, G; Siciliano, Gabriele; Nichelli, P; Murri, Luigi | |
Proton MR spectroscopy of mitochondrial diseases: analysis of brain metabolic abnormalities and their possible diagnostic relevance | 1-gen-2003 | Bianchi, M. C.; Tosetti, M.; Battini, R.; Manca, MARIA LAURA; Mancuso, Michelangelo; Cioni, Giovanni; Canapicchi, R.; Siciliano, Gabriele | |
Proton MR Spectroscopy of mitochondrial diseases: Analysis of brain metabolic abnormalities and their possible diagnostic relevance | 1-gen-2003 | Bianchi, Mc; Tosetti, M; Battini, R; Mancuso, M; Cioni, G; Canapicchi, R and Siciliano G | |
AUTOSOMAL DOMINANT EXTERNAL OPHTHALMOPLEGIA AND BIPOLAR AFFECTIVE DISORDER ASSOCIATED WITH A MUTATION IN THE ANT1 GENE | 1-gen-2003 | Siciliano, Gabriele; Tessa, A; Petrini, S; Mancuso, Michelangelo; Bruno, C; Grieco, Gs; Malandrini, A; Deflorio, L; Martini, B; Federico, A; Nappi, G; Santorelli, Fm; Murri, Luigi | |
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? | 1-gen-2004 | Mancuso, Michelangelo; Murri, Luigi; Rocchi, A; Tessitore, A; Muglia, M; Tedeschi, G; Panza, D; Monsurr, Mr; Sola, P; Mandrioli, J; Choub, A; Delcorona, A; Manca, MARIA LAURA; Mazzei, Rl; Sprovieri, T; Filosto, M; Salviati, A; Valentino, P; Bono, F; Caracciolo, M; Simone, Il; LA BELLA, V; Majorana, G; Siciliano, Gabriele; Murri, L; Quattrone, A. | |
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome | 1-gen-2004 | Mancuso, Michelangelo; Filosto, M; Mootha, Vk; Rocchi, A; Pistolesi, S; Murri, Luigi; Dimauro, S; Siciliano, Gabriele |
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