Sfoglia per Autore
T-cell anti-apoptotic mechanisms in inflammatory myopathies
2000-01-01 Vattemi, G.; Tonin, P.; Filosto, M.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G.
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy
2001-01-01 Zanusso, G.; Vattemi, G.; Ferrari, S.; Tabaton, M.; Pecini, E.; Cavallaro, T.; Tomelleri, G.; Filosto, M.; Tonin, P.; Nardelli, E.; Rizzuto, N.; Monaco, S.
A new mutation in the mitochondrial tRNAAla gene in a patient with ophthalmoplegia and dysphagia
2001-01-01 Spagnolo, M.; Tomelleri, G.; Vattemi, G.; Filosto, M.; Rizzuto, N.; Tonin, P.
Dermatomyositis and retroperitoneal germ cell cancer
2001-01-01 Vattemi, G.; Tonin, P.; Martignoni, G.; Filosto, M.; Marchioretto, F.; Rizzuto, N.; Tomelleri, G.
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: A case report
2001-01-01 Filosto, M.; Tonin, P.; Vattemi, G.; Bongiovanni, L. G.; Rizzuto, N.; Tomelleri, G.
Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis
2001-01-01 Filosto, M.; Bertolasi, L.; Fincati, E.; Priori, A.; Tomelleri, G.; Chieregato, G.; Rizzuto, N.
A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis
2002-01-01 Mancuso, M.; Filosto, M.; Naini, A.; Rocchi, A.; Del Corona, A.; Sartucci, F.; Siciliano, G.; Murri, L.
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases
2002-01-01 Filosto, M.; Tonin, P.; Vattemi, G.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G.
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes
2003-01-01 Mancuso, M.; Filosto, M.; Tsujino, S.; Lamperti, C.; Shanske, S.; Coquet, M.; Desnuelle, C.; Dimauro, S.
Reversible upper limb muscle weakness with selective loss of thick filaments
2003-01-01 Vattemi, G.; Tonin, P.; Filosto, M.; Savio, C.; Rizzuto, N.; Tomelleri, G.
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases
2003-01-01 Filosto, M.; Tonin, P.; Vattemi, G.; Savio, C.; Rizzuto, N.; Tomelleri, G.
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ
2003-01-01 Filosto, M.; Mancuso, M.; Nishigaki, Y.; Pancrudo, J.; Harati, Y.; Gooch, C.; Mankodi, A.; Bayne, L.; Bonilla, E.; Shanske, S.; Hirano, M.; Dimauro, S.
P301L Tau mutation and non-Alzheimer dementias in Italy
2003-01-01 Mancuso, M.; Leone, M.; Filosto, M.; Tognoni, G.; Siciliano, G.; Nichelli, P.; Murri, L.
Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene
2003-01-01 Mancuso, M.; Filosto, M.; Bonilla, E.; Hirano, M.; Shanske, S.; Vu, T. H.; Dimauro, S.
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease)
2003-01-01 Simonati, A.; Filosto, M.; Savio, C.; Tomelleri, G.; Tonin, P.; Dalla Bernardina, B.; Rizzuto, N.
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies
2003-01-01 Filosto, M.; Mancuso, M.; Vives-Bauza, C.; Vila, M. R.; Shanske, S.; Hirano, M.; Andreu, A. L.; Dimauro, S.
Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene
2003-01-01 Mancuso, M.; Filosto, M.; Stevens, J. C.; Patterson, M.; Shanske, S.; Krishna, S.; Dimauro, S.
Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251
2003-01-01 Mancuso, M.; Filosto, M.; Hirano, M.; Dimauro, S.
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease
2003-01-01 Simonati, A.; Filosto, M.; Tomelleri, G.; Savio, C.; Tonin, P.; Polo, A.; Rizzuto, N.
Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease
2003-01-01 Mancuso, M.; Filosto, M.; Bosetti, F.; Ceravolo, R.; Rocchi, A.; Tognoni, G.; Manca, M. L.; Solaini, G.; Siciliano, G.; Murri, L.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| T-cell anti-apoptotic mechanisms in inflammatory myopathies | 1-gen-2000 | Vattemi, G.; Tonin, P.; Filosto, M.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G. | |
| Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy | 1-gen-2001 | Zanusso, G.; Vattemi, G.; Ferrari, S.; Tabaton, M.; Pecini, E.; Cavallaro, T.; Tomelleri, G.; Filosto, M.; Tonin, P.; Nardelli, E.; Rizzuto, N.; Monaco, S. | |
| A new mutation in the mitochondrial tRNAAla gene in a patient with ophthalmoplegia and dysphagia | 1-gen-2001 | Spagnolo, M.; Tomelleri, G.; Vattemi, G.; Filosto, M.; Rizzuto, N.; Tonin, P. | |
| Dermatomyositis and retroperitoneal germ cell cancer | 1-gen-2001 | Vattemi, G.; Tonin, P.; Martignoni, G.; Filosto, M.; Marchioretto, F.; Rizzuto, N.; Tomelleri, G. | |
| Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: A case report | 1-gen-2001 | Filosto, M.; Tonin, P.; Vattemi, G.; Bongiovanni, L. G.; Rizzuto, N.; Tomelleri, G. | |
| Axillary injection of botulinum A toxin in a patient with muscle cramps associated with severe axillary hyperhidrosis | 1-gen-2001 | Filosto, M.; Bertolasi, L.; Fincati, E.; Priori, A.; Tomelleri, G.; Chieregato, G.; Rizzuto, N. | |
| A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis | 1-gen-2002 | Mancuso, M.; Filosto, M.; Naini, A.; Rocchi, A.; Del Corona, A.; Sartucci, F.; Siciliano, G.; Murri, L. | |
| Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases | 1-gen-2002 | Filosto, M.; Tonin, P.; Vattemi, G.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G. | |
| Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes | 1-gen-2003 | Mancuso, M.; Filosto, M.; Tsujino, S.; Lamperti, C.; Shanske, S.; Coquet, M.; Desnuelle, C.; Dimauro, S. | |
| Reversible upper limb muscle weakness with selective loss of thick filaments | 1-gen-2003 | Vattemi, G.; Tonin, P.; Filosto, M.; Savio, C.; Rizzuto, N.; Tomelleri, G. | |
| Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mitochondrial diseases | 1-gen-2003 | Filosto, M.; Tonin, P.; Vattemi, G.; Savio, C.; Rizzuto, N.; Tomelleri, G. | |
| Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase γ | 1-gen-2003 | Filosto, M.; Mancuso, M.; Nishigaki, Y.; Pancrudo, J.; Harati, Y.; Gooch, C.; Mankodi, A.; Bayne, L.; Bonilla, E.; Shanske, S.; Hirano, M.; Dimauro, S. | |
| P301L Tau mutation and non-Alzheimer dementias in Italy | 1-gen-2003 | Mancuso, M.; Leone, M.; Filosto, M.; Tognoni, G.; Siciliano, G.; Nichelli, P.; Murri, L. | |
| Mitochondrial myopathy of childhood associated with mitochondrial DNA depletion and a homozygous mutation (T77M) in the TK2 gene | 1-gen-2003 | Mancuso, M.; Filosto, M.; Bonilla, E.; Hirano, M.; Shanske, S.; Vu, T. H.; Dimauro, S. | |
| Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) | 1-gen-2003 | Simonati, A.; Filosto, M.; Savio, C.; Tomelleri, G.; Tonin, P.; Dalla Bernardina, B.; Rizzuto, N. | |
| Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies | 1-gen-2003 | Filosto, M.; Mancuso, M.; Vives-Bauza, C.; Vila, M. R.; Shanske, S.; Hirano, M.; Andreu, A. L.; Dimauro, S. | |
| Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene | 1-gen-2003 | Mancuso, M.; Filosto, M.; Stevens, J. C.; Patterson, M.; Shanske, S.; Krishna, S.; Dimauro, S. | |
| Spinal muscular atrophy and mitochondrial DNA depletion. Response to Berber et al. (2003) Acta Neuropathol 105:245-251 | 1-gen-2003 | Mancuso, M.; Filosto, M.; Hirano, M.; Dimauro, S. | |
| Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease | 1-gen-2003 | Simonati, A.; Filosto, M.; Tomelleri, G.; Savio, C.; Tonin, P.; Polo, A.; Rizzuto, N. | |
| Decreased platelet cytochrome c oxidase activity is accompanied by increased blood lactate concentration during exercise in patients with Alzheimer disease | 1-gen-2003 | Mancuso, M.; Filosto, M.; Bosetti, F.; Ceravolo, R.; Rocchi, A.; Tognoni, G.; Manca, M. L.; Solaini, G.; Siciliano, G.; Murri, L. |
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