1.1 Articolo in rivista

1.1 Articolo in rivista: [48025] Home page tipologia

Sfoglia

Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 15.961 a 15.980 di 48.025

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.

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.

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.

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.

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.

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.

A novel mitochondrial tRNAPhe mutation causes MERRF syndrome

2004-01-01 Mancuso, M.; Filosto, M.; Mootha, V. K.; Rocchi, A.; Pistolesi, S.; Murri, L.; Dimauro, S.; Siciliano, G.

A novel polymerase γ mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism

2004-01-01 Mancuso, M.; Filosto, M.; Oh, S. J.; Dimauro, S.

POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness

2004-01-01 Mancuso, M.; Filosto, M.; Bellan, M.; Liguori, R.; Montagna, P.; Baruzzi, A.; Dimauro, S.; Carelli, V.

Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?

2004-01-01 Mancuso, M.; Conforti, F. L.; Rocchi, A.; Tessitore, A.; Muglia, M.; Tedeschi, G.; Panza, D.; Monsurro, M.; Sola, P.; Mandrioli, J.; Choub, A.; Delcorona, A.; Manca, M. L.; Mazzei, R.; Sprovieri, T.; Filosto, M.; Salviati, A.; Valentino, P.; Bono, F.; Caracciolo, M.; Simone, I. L.; La Bella, V.; Majorana, G.; Siciliano, G.; Murri, L.; Quattrone, A.

Expression of protein-kinase C isoforms and interleukin-1β in myofibrillar myopathy

2004-01-01 Vattemi, G.; Tonin, P.; Mora, M.; Filosto, M.; Morandi, L.; Savio, C.; Dal Pra, I.; Rizzuto, N.; Tomelleri, G.

A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome

2004-01-01 Mancuso, M.; Vives-Bauza, C.; Filosto, M.; Marti, R.; Solano, A.; Montoya, J.; Gamez, J.; Dimauro, S.; Andreu, A. L.

Hepato-cerebral syndrome: Genetic and pathological studies in an infant with a dGK mutation

2004-01-01 Filosto, M.; Mancuso, M.; Tomelleri, G.; Rizzuto, N.; Bernardina, B. D.; Dimauro, S.; Simonati, A.

A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation

2004-01-01 Mancuso, M.; Filosto, M.; Forli, F.; Rocchi, A.; Berrettini, S.; Siciliano, G.; Murri, L.

Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy

2005-01-01 Vattemi, G.; Tomelleri, G.; Filosto, M.; Savio, C.; Rizzuto, N.; Tonin, P.

Human skeletal muscle as a target organ of trichloroethylene toxicity

2005-01-01 Vattemi, G.; Tonin, P.; Filosto, M.; Rizzuto, N.; Tomelleri, G.; Perbellini, L.; Iacovelli, W.; Petrucci, N.

Progressive external ophthalmoplegia: A new family with tremor and peripheral neuropathy [1]

2005-01-01 Hisama, F. M.; Mancuso, M.; Filosto, M.; Dimauro, S.

Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-γA

2005-01-01 Ferrari, G.; Lamantea, E.; Donati, A.; Filosto, M.; Briem, E.; Carrara, F.; Parini, R.; Simonati, A.; Sanier, R.; Zeviani, M.

Mitochondrial dysfunction and Alzheimer's disease: New developments

2006-01-01 Mancuso, M.; Siciliano, G.; Filosto, M.; Murri, L.

Antimyoclonic effect of levetiracetam in MERRF syndrome

2006-01-01 Mancuso, M.; Galli, R.; Pizzanelli, C.; Filosto, M.; Siciliano, G.; Murri, L.

Titolo	Data di pubblicazione	Autore(i)
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.
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.
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.
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.
A novel mitochondrial tRNAPhe mutation causes MERRF syndrome	1-gen-2004	Mancuso, M.; Filosto, M.; Mootha, V. K.; Rocchi, A.; Pistolesi, S.; Murri, L.; Dimauro, S.; Siciliano, G.
A novel polymerase γ mutation in a family with ophthalmoplegia, neuropathy, and parkinsonism	1-gen-2004	Mancuso, M.; Filosto, M.; Oh, S. J.; Dimauro, S.
POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness	1-gen-2004	Mancuso, M.; Filosto, M.; Bellan, M.; Liguori, R.; Montagna, P.; Baruzzi, A.; Dimauro, S.; Carelli, V.
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis?	1-gen-2004	Mancuso, M.; Conforti, F. L.; Rocchi, A.; Tessitore, A.; Muglia, M.; Tedeschi, G.; Panza, D.; Monsurro, M.; Sola, P.; Mandrioli, J.; Choub, A.; Delcorona, A.; Manca, M. L.; Mazzei, R.; Sprovieri, T.; Filosto, M.; Salviati, A.; Valentino, P.; Bono, F.; Caracciolo, M.; Simone, I. L.; La Bella, V.; Majorana, G.; Siciliano, G.; Murri, L.; Quattrone, A.
Expression of protein-kinase C isoforms and interleukin-1β in myofibrillar myopathy	1-gen-2004	Vattemi, G.; Tonin, P.; Mora, M.; Filosto, M.; Morandi, L.; Savio, C.; Dal Pra, I.; Rizzuto, N.; Tomelleri, G.
A mitochondrial DNA duplication as a marker of skeletal muscle specific mutations in the mitochondrial genome	1-gen-2004	Mancuso, M.; Vives-Bauza, C.; Filosto, M.; Marti, R.; Solano, A.; Montoya, J.; Gamez, J.; Dimauro, S.; Andreu, A. L.
Hepato-cerebral syndrome: Genetic and pathological studies in an infant with a dGK mutation	1-gen-2004	Filosto, M.; Mancuso, M.; Tomelleri, G.; Rizzuto, N.; Bernardina, B. D.; Dimauro, S.; Simonati, A.
A non-syndromic hearing loss caused by very low levels of the mtDNA A3243G mutation	1-gen-2004	Mancuso, M.; Filosto, M.; Forli, F.; Rocchi, A.; Berrettini, S.; Siciliano, G.; Murri, L.
Expression of late myogenic differentiation markers in sarcoplasmic masses of patients with myotonic dystrophy	1-gen-2005	Vattemi, G.; Tomelleri, G.; Filosto, M.; Savio, C.; Rizzuto, N.; Tonin, P.
Human skeletal muscle as a target organ of trichloroethylene toxicity	1-gen-2005	Vattemi, G.; Tonin, P.; Filosto, M.; Rizzuto, N.; Tomelleri, G.; Perbellini, L.; Iacovelli, W.; Petrucci, N.
Progressive external ophthalmoplegia: A new family with tremor and peripheral neuropathy [1]	1-gen-2005	Hisama, F. M.; Mancuso, M.; Filosto, M.; Dimauro, S.
Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-γA	1-gen-2005	Ferrari, G.; Lamantea, E.; Donati, A.; Filosto, M.; Briem, E.; Carrara, F.; Parini, R.; Simonati, A.; Sanier, R.; Zeviani, M.
Mitochondrial dysfunction and Alzheimer's disease: New developments	1-gen-2006	Mancuso, M.; Siciliano, G.; Filosto, M.; Murri, L.
Antimyoclonic effect of levetiracetam in MERRF syndrome	1-gen-2006	Mancuso, M.; Galli, R.; Pizzanelli, C.; Filosto, M.; Siciliano, G.; Murri, L.

Prodotti della tipologia (ordinati per Data di deposito in Decrescente ordine): 15.961 a 15.980 di 48.025

Legenda icone

file ad accesso aperto
file disponibili sulla rete interna
file disponibili agli utenti autorizzati
file disponibili solo agli amministratori
file sotto embargo
nessun file disponibile

Scopri

Accesso al fulltext

no fulltext31384
open7285
reserved5941
restricted3344
partially open51
embargoed15
mixed5

IRIS Institutional Research Information System - OPENBS Open Archive UniBS