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T-cell anti-apoptotic mechanisms in inflammatory myopathies 1-gen-2000 Vattemi, G.; Tonin, P.; Filosto, M.; Spagnolo, M.; Rizzuto, N.; Tomelleri, G.
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.
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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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