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DE MARCO, ELVIRA VALERIA

DE MARCO, ELVIRA VALERIA  

Istituto per la Ricerca e l'Innovazione Biomedica -IRIB  

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Titolo Data di pubblicazione Autore(i) File
A WHOLE mtDNA NGS APPROACH TO IDENTIFY NOVEL VARIANTS IN PATIENTS AFFECTED BY MITOCHONDRIAL DISEASES 1-gen-2019 DE MARCO, ELVIRA VALERIA; Citrigno, L; DE BENEDITTIS, Selene; Cerantonio, A; DI PALMA, Gemma; Cittadella, R
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders 1-gen-2018 La Cognata, Valentina; Morello, Giovanna; Gentile, Giulia; Cavalcanti, Francesca; Cittadella, Rita; Conforti, Francesca Luisa; De Marco, Elvira Valeria; Magariello, Angela; Muglia, Maria; Patitucci, Alessandra; Spadafora, Patrizia; D'Agata, Velia; Ruggieri, Martino; Cavallaro, Sebastiano
Copy Number Variants in Alzheimer's Disease 1-gen-2017 Cuccaro, Denis; De Marco, Elvira Valeria; Cittadella, Rita; Cavallaro, Sebastiano
McLeod syndrome in an Italian patient 1-gen-2017 E.V. De Marco; R. Cittadella; B. Minafra; F. Avantaggiato; R. Zangaglia; C. Pacchetti
Huntington's disease-like syndrome: a case report 1-gen-2016 Avantaggiato, F; Minafra, B; Zangaglia, R; De Marco, Ev; Cittadella, R; Pacchetti, C
La sindrome di Mc Leod: un caso clinico 1-gen-2016 Cittadella, R; Avantaggiato, F; Minafra, B; Zangaglia, R; Pacchetti, C; De Marco, Ev
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease a multicenter study. 1-gen-2014 von Otter, M; Bergström, P; Quattrone, A; De Marco, E; Annesi, G; Söderkvist, P; Wettinger, S; Drozdzik, M; Bialecka, M; Nissbrandt, H; Klein, C; Nilsson, M; Hammarsten, O; Nilsson, S; Zetterberg, H
Potential involvement of GRIN2B encoding the NMDA receptor subunit NR2B in the spectrum of Alzheimer's disease 1-gen-2014 Andreoli, Virginia; DE MARCO, ELVIRA VALERIA; Trecroci, Francesca; Cittadella, Rita; DI PALMA, Gemma; Gambardella, Antonio
Role of the Neuregulin 1 gene (NRG1) in multiple sclerosis 1-gen-2014 Cittadella, R; Andreoli, V; Trecroci, F; DI PALMA, Gemma; DE MARCO, ELVIRA VALERIA
A multicenter study of glucocerebrosidase mutations in dementia with lewy bodies. 1-gen-2013 Nalls MA; Duran R; Lopez G; KurzawaAkanbi M; McKeith IG; Chinnery PF; Morris CM; Theuns J; Crosiers D; Cras P; Engelborghs S; De Deyn PP; Van Broeckhoven C; Mann DM; Snowden J; PickeringBrown S; Halliwell N; Davidson Y; Gibbons L; Harris J; Sheerin UM; Bras J; Hardy J; Clark L; Marder K; Honig LS; Berg D; Maetzler W; Brockmann K; Gasser T; Novellino F; Quattrone A; Annesi G; De Marco EV; Rogaeva E; Masellis M; Black SE; Bilbao JM; Foroud T; Ghetti B; Nichols WC; Pankratz N; Halliday G; Lesage S; Klebe S; Durr A; Duyckaerts C; Brice A; Giasson BI; Trojanowski JQ; Hurtig HI; Tayebi N; Landazabal C; Knight MA; Keller M; Singleton AB; Wolfsberg TG; Sidransky E.
Ruolo del gene Neuregulin 1 (NRG1) nella Sclerosi Multipla 1-gen-2013 E. V. De Marco; V. Andreoli; F. Trecroci; G. Di Palma; R. Cittadella
Associazione tra la subunità 2B del recettore NMDA (gene GRIN2B) e la malattia di Alzheimer 1-gen-2012 Trecroci, F; Cittadella, R; De Marco, Ev; Liguori, M; Spadafora, P; DI PALMA, Gemma; Andreoli, V
Mutation analysis of the GRIN2B gene in Alzheimer's disease 1-gen-2012 F. Trecroci; R. Cittadella; E. V. De Marco; M. Liguori; P. Spadafora; G. Di Palma; V. Andreoli.
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 1-gen-2012 Scornaienchi, V; Civitelli, D; De Marco, Ev; Annesi, G; Tarantino, P; Rocca, Fe; Greco, V; Provenzano, G; Annesi, F; Nicoletti, G; Colica, C; Uncini, A; Salsone, M; Novellino, F; Morelli, M; Arabia, G; Gambardella, A; Quattrone, A
Spinocerebellar ataxia type 7: report of a new Italian family. 1-gen-2012 Italiano, D; Tarantino, P; De Marco, Ev; Calabrò, Rs; Bramanti, P; Quattrone, A; Annesi, G
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy. 1-gen-2011 Greco, V; De Marco, Ev; Rocca, Fe; Annesi, F; Civitelli, D; Provenzano, G; Tarantino, P; Scornaienchi, V; Pucci, F; Salsone, M; Novellino, F; Morelli, M; Paglionico, S; Gambardella, A; Quattrone, A; Annesi, G
Association study between the LINGO1 gene and Parkinson s disease in the Italian population 1-gen-2011 Annesi F; De Marco EV; Rocca FE; Nicoletti A; Pugliese P; Nicoletti G; Arabia G; Tarantino P; De Mari M; Lamberti P; Gallerini S; Marconi R; Epifanio A; Morgante L; Cozzolino A; Barone P; Torchia G; Zappia M; Annesi G; Quattrone A.
Lack of association between G-protein coupled receptor kinase 5 gene and Parkinson's disease 1-gen-2011 Tarantino, P; V De Marco, E; E Rocca, F; Annesi, F; Civitelli, D; Provenzano, G; Scornaienchi, V; Greco, V; Colica, C; Nicoletti, G; Quattrone, A; Annesi, G
A comprehensive mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism. 1-gen-2010 V De Marco, E; Scornaienchi, V; Tarantino, P; E Rocca, F; Greco, V; Provenzano, G; Civitelli D, D; Annesi, F; Nicoletti, G; Uncini, A; Quattrone, A; Annesi, G
Association study between G-protein-coupled receptor kinase 5 gene and Parkinson s disease 1-gen-2010 P. Tarantino; E. V. De Marco; F. E. Rocca; F. Annesi; D. Civitelli; G. Provenzano; V. Scornaienchi; V. Greco; A. Gambardella; A. Quattrone; G. Annesi.