IRIS

PETRUZZELLA, Vittoria

PETRUZZELLA, Vittoria  

DIPARTIMENTO DI BIOMEDICINA TRASLAZIONALE E NEUROSCIENZE  

Mostra records
Risultati 1 - 20 di 118 (tempo di esecuzione: 0.051 secondi).
Titolo Data di pubblicazione Autore(i) File
A Gel-Based Proteomic Analysis Reveals Synovial α-Enolase and Fibrinogen β-Chain Dysregulation in Knee Osteoarthritis: A Controlled Trial 1-gen-2023 Rocchetti, Maria Teresa; Bizzoca, Davide; Moretti, Lorenzo; Ragni, Enrico; Moretti, Francesco Luca; Vicenti, Giovanni; Solarino, Giuseppe; Rizzello, Alessandro; Petruzzella, Vittoria; Palese, Luigi Leonardo; Scacco, Salvatore; Banfi, Giuseppe; Moretti, Biagio; Gnoni, Antonio
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1H 1-gen-2010 Bisceglia, L; Zoccolella, S; Torraco, A; Piemontese, Mr; Dell'Aglio, R; Amati, A; De Bonis, P; Artuso, L; Copetti, M; Santorelli, Fm; Serlenga, L; Zelante, L; Bertini, E; Petruzzella, Vittoria
A nonsense mutation in the NDUFS4 gene encoding the 18 kDa (AQDQ) subunit of complex I abolishes assembly and activity of the complex in a patient with Leigh-like syndrome 1-gen-2001 Petruzzella, Vittoria; Vergari, R; Puzziferri, I; Boffoli, D; Lamantea, E; Zeviani, M; Papa, S.
A novel insertion mutation (A(169i)) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient 1-gen-1998 Santorelli, Fm; Bertini, E; Petruzzella, Vittoria; Di Capua, M; Calvieri, S; Gasparini, P; Zeviani, M.
A novel mutation in the LRSAM1 gene in a family with early onset autosomal dominant Charcot-Marie-Tooth type 2P 1-gen-2024 Milella, G.; Amati, A.; Lastella, P.; Zanfardino, P.; Petruzzella, V.; Zoccolella, S.
ACETYL-L-CARNITINE INCREASES CYTOCHROME-OXIDASE SUBUNIT-I MESSENGER-RNA CONTENT IN HYPOTHYROID RAT-LIVER 1-gen-1990 Gadaleta, Mn; Petruzzella, Vittoria; Fracasso, F; Fernandezsilva, P; Cantatore, Palmiro
ACTN3/ACE GENOTYPES AND MITOCHONDRIAL GENOME IN PROFESSIONAL SOCCER PLAYERS’ PERFORMANCE 1-gen-2017 Valeria, Galeandro; Notarnicola, Angela; Bianco, Angelica; Tafuri, Silvio; Russo, Luciana; Pesce, Vito; Moretti, Biagio; Petruzzella, Vittoria
Additive effects of genetic variation in dopamine regulating genes on working memory cortical activity in human brain 1-gen-2006 Bertolino, A.; Blasi, G.; Latorre, V.; Rubino, V.; Rampino, A.; Sinibaldi, L.; Caforio, G.; Petruzzella, V.; Pizzuti, A.; Scarabino, T.; Nardini, M.; Weinberger, D. R.; Dallapiccola, B.
Age-dependent structural variations in rat brain mitochondrial DNA 1-gen-1992 Petruzzella, Vittoria; Fracasso, F; Gadaleta, Mn; Cantatore, Palmiro
Alteration of mitochondrial DNA and RNA level in human fibroblasts with impaired vitamin B12 coenzyme synthesis 1-gen-1998 Cantatore, Palmiro; Petruzzella, Vittoria; Nicoletti, C; Papadia, F; Fracasso, F; Rustin, P; Gadaleta, Mn
ALTERAZIONI STRUTTURALI DEL DNA MITOCONDRIALE IN TESSUTI DI RATTO VECCHIO 1-gen-1993 Gadaleta, M. N.; Rainaldi, Guglielmo; Lezza, Angela Maria Serena; Petruzzella, Vittoria; G. RAINALDI E. P., Cantatore
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 1-gen-2004 Petruzzella, Vittoria; Panelli, D; Torraco, A; Iuso, A; Scacco, Salvatore; Papa, S.
Alternative splicing and nonsense-mediated mRNA decay in genetic disorder of complex I 1-gen-2004 Petruzzella, Vittoria; Panelli, D; Torraco, A; Iuso, A; Scacco, Salvatore; Papa, S.
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunit 1-gen-2003 Petruzzella, Vittoria; Di Giacinto, G; Scacco, Salvatore; Piemonte, F; Torraco, A; Carrozzo, R; Vergari, R; Dionisi Vici, C; Longo, D; Tessa, A; Papa, S; Bertini, E.
Author response: Do high mtDNA copy numbers truly prevent LHON manifestations? 1-gen-2017 Bianco, Angelica; Petruzzella, Vittoria
Author Response: Increased mtDNA Copy Number Protects Against LHON 1-gen-2018 Bianco, Angelica; Palese, Luigi L.; Guerriero, Silvana; Petruzzella, Vittoria
Autophagy and proliferation are dysregulated in Charcot-Marie-Tooth disease type 2A cells harboring MFN2 (mitofusin 2) mutation 1-gen-2022 Zanfardino, Paola; Petruzzella, Vittoria
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction 1-gen-2021 Berti, B.; Longo, G.; Mari, F.; Doccini, S.; Piccolo, I.; Donati, M. A.; Moro, F.; Guerrini, R.; Santorelli, F. M.; Petruzzella, V.
Bilateral progressive visual loss in an epileptic, mentally retarded boy 1-gen-2011 Guerriero, Silvana; Vetrugno, Michele; Ciracì, L; Artuso, L; Dell'Aglio, R; Petruzzella, Vittoria
Bilateral striatal necrosis, dystonia and multiple mitochondrial DNA deletions: case study and effect of deep brain stimulation 1-gen-2008 Aniello, Ms; Martino, D; Petruzzella, Vittoria; Eleopra, R; Mancuso, M; Dell'Aglio, R; Cavallo, M; Siciliano, G; Defazio, Giovanni