DE MARCO, ELVIRA VALERIA
DE MARCO, ELVIRA VALERIA
Istituto per la Ricerca e l'Innovazione Biomedica -IRIB
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders
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
2017 Cuccaro, Denis; De Marco, Elvira Valeria; Cittadella, Rita; Cavallaro, Sebastiano
Huntington's disease-like syndrome: a case report
2016 Avantaggiato, F; Minafra, B; Zangaglia, R; De Marco, Ev; Cittadella, R; Pacchetti, C
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease a multicenter study.
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
2014 Andreoli, Virginia; DE MARCO, ELVIRA VALERIA; Trecroci, Francesca; Cittadella, Rita; DI PALMA, Gemma; Gambardella, Antonio
A multicenter study of glucocerebrosidase mutations in dementia with lewy bodies.
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.
Mutation analysis of the PINK1 gene in Southern Italian patients with early- and late-onset parkinsonism.
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.
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.
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
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
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
Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism"
2010 Tarantino, Patrizia; Civitelli, Donatella; Annesi, Ferdinanda; De Marco Elvira, V; Rocca Francesca, E; Pugliese, Pierfrancesco; Nicoletti, Giuseppe; Carrideo, Sara; Provenzano, Giovanni; Annesi, Grazia; Quattrone, Aldo
DJ-1 is a Parkinson's disease susceptibility gene in southern Italy.
2010 De Marco, Ev; Annesi, G; Tarantino, P; Nicoletti, G; Civitelli, D; Messina, D; Annesi, F; Arabia, G; Salsone, M; Condino, F; Novellino, F; Provenzano, G; Rocca, Fe; Colica, C; Morelli, M; Scornaienchi, V; Greco, V; Giofrè, L; Quattrone, A
Myocardial (123)I-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD.
2010 Novellino, F; Bagnato, A; Salsone, M; Cascini, Gl; Nicoletti, G; Arabia, G; Pugliese, P; Morelli, M; Paglionico, S; Cipullo, S; Manna, I; De Marco, Ev; Condino, F; Chiriaco, C; Morgante, L; Zappia, M; Quattrone, A
Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.
2010 La Russa, A; Cittadella, R; De Marco, Ev; Valentino, P; Andreoli, V; Trecroci, F; Latorre, V; Gambardella, A; Quattrone, A
Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism.
2009 Tarantino, P; Civitelli, D; Annesi, F; DE MARCO, ELVIRA VALERIA; Rocca, Fe; Pugliese, P; Nicoletti, G; Carrideo, S; Provenzano, G; Annesi, G; Quattrone, A
HOMER1 promoter analysis in Parkinson's disease: association study with psychotic symptoms.
2009 De Luca V; Annesi G; De Marco EV; de Bartolomeis A; Nicoletti G; Pugliese P; Muscettola G; Barone P; Quattrone A.
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
2009 Sidransky, E; Nalls, Ma; Aasly, Jo; Aharonperetz, J; Annesi, G; Barbosa, Er; Barshira, A; Berg, D; Bras, J; Brice, A; Chen, Cm; Clark, Ln; Condroyer, C; DE MARCO, ELVIRA VALERIA; Dürr, A; Eblan, Mj; Fahn, S; Farrer, Mj; Fung, Hc; Ganor, Z; Gasser, T; Gershonibaruch, R; Giladi, N; Griff,
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.
2009 Sidransky E; Nalls MA; Aasly JO; AharonPeretz J; Annesi G; Barbosa ER; BarShira A; Berg D; Bras J; Brice A; Chen CM; Clark LN; Condroyer C; De Marco EV; Dürr A; Eblan MJ; Fahn S; Farrer MJ; Fung HC; GanOr Z; Gasser T; GershoniBaruch R; Giladi N; Griffith A; Gurevich T; Januario C; Kropp P; Lang AE; LeeChen GJ; Lesage S; Marder K; Mata IF; Mirelman A; Mitsui J; Mizuta I; Nicoletti G; Oliveira C; Ottman R; OrrUrtreger A; Pereira LV; Quattrone A; Rogaeva E; Rolfs A; Rosenbaum H; Rozenberg R; Samii A; Samaddar T; Schulte C; Sharma M; Singleton A; Spitz M; Tan EK; Tayebi N; Toda T; Troiano AR; Tsuji S; Wittstock M; Wolfsberg TG; Wu YR; Zabetian CP; Zhao Y; Ziegler SG.
Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy.
2009 Provenzano G; Mannarino E; Annesi F; De Marco EV; Rocca FE; Greco V; Scornaienchi V; Tarantino P; Civitelli D; Quattrone A; Tortorella G; Annesi G.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 | |
| Huntington's disease-like syndrome: a case report | 1-gen-2016 | Avantaggiato, F; Minafra, B; Zangaglia, R; De Marco, Ev; Cittadella, R; Pacchetti, C | |
| 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 | |
| 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. | |
| 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 | |
| Author's reply to the comment of Sironi et al. on "Compound heterozygosity in DJ-1 gene non-coding portion related to Parkinsonism" | 1-gen-2010 | Tarantino, Patrizia; Civitelli, Donatella; Annesi, Ferdinanda; De Marco Elvira, V; Rocca Francesca, E; Pugliese, Pierfrancesco; Nicoletti, Giuseppe; Carrideo, Sara; Provenzano, Giovanni; Annesi, Grazia; Quattrone, Aldo | |
| DJ-1 is a Parkinson's disease susceptibility gene in southern Italy. | 1-gen-2010 | De Marco, Ev; Annesi, G; Tarantino, P; Nicoletti, G; Civitelli, D; Messina, D; Annesi, F; Arabia, G; Salsone, M; Condino, F; Novellino, F; Provenzano, G; Rocca, Fe; Colica, C; Morelli, M; Scornaienchi, V; Greco, V; Giofrè, L; Quattrone, A | |
| Myocardial (123)I-MIBG scintigraphy for differentiation of Lewy bodies disease from FTD. | 1-gen-2010 | Novellino, F; Bagnato, A; Salsone, M; Cascini, Gl; Nicoletti, G; Arabia, G; Pugliese, P; Morelli, M; Paglionico, S; Cipullo, S; Manna, I; De Marco, Ev; Condino, F; Chiriaco, C; Morgante, L; Zappia, M; Quattrone, A | |
| Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study. | 1-gen-2010 | La Russa, A; Cittadella, R; De Marco, Ev; Valentino, P; Andreoli, V; Trecroci, F; Latorre, V; Gambardella, A; Quattrone, A | |
| Compound heterozygosity in DJ-1 gene non-coding portion related to parkinsonism. | 1-gen-2009 | Tarantino, P; Civitelli, D; Annesi, F; DE MARCO, ELVIRA VALERIA; Rocca, Fe; Pugliese, P; Nicoletti, G; Carrideo, S; Provenzano, G; Annesi, G; Quattrone, A | |
| HOMER1 promoter analysis in Parkinson's disease: association study with psychotic symptoms. | 1-gen-2009 | De Luca V; Annesi G; De Marco EV; de Bartolomeis A; Nicoletti G; Pugliese P; Muscettola G; Barone P; Quattrone A. | |
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. | 1-gen-2009 | Sidransky, E; Nalls, Ma; Aasly, Jo; Aharonperetz, J; Annesi, G; Barbosa, Er; Barshira, A; Berg, D; Bras, J; Brice, A; Chen, Cm; Clark, Ln; Condroyer, C; DE MARCO, ELVIRA VALERIA; Dürr, A; Eblan, Mj; Fahn, S; Farrer, Mj; Fung, Hc; Ganor, Z; Gasser, T; Gershonibaruch, R; Giladi, N; Griff, | |
| Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. | 1-gen-2009 | Sidransky E; Nalls MA; Aasly JO; AharonPeretz J; Annesi G; Barbosa ER; BarShira A; Berg D; Bras J; Brice A; Chen CM; Clark LN; Condroyer C; De Marco EV; Dürr A; Eblan MJ; Fahn S; Farrer MJ; Fung HC; GanOr Z; Gasser T; GershoniBaruch R; Giladi N; Griffith A; Gurevich T; Januario C; Kropp P; Lang AE; LeeChen GJ; Lesage S; Marder K; Mata IF; Mirelman A; Mitsui J; Mizuta I; Nicoletti G; Oliveira C; Ottman R; OrrUrtreger A; Pereira LV; Quattrone A; Rogaeva E; Rolfs A; Rosenbaum H; Rozenberg R; Samii A; Samaddar T; Schulte C; Sharma M; Singleton A; Spitz M; Tan EK; Tayebi N; Toda T; Troiano AR; Tsuji S; Wittstock M; Wolfsberg TG; Wu YR; Zabetian CP; Zhao Y; Ziegler SG. | |
| Novel human pathological mutations. Gene symbol: SCN1A. Disease: severe myoclonic epilepsy of infancy. | 1-gen-2009 | Provenzano G; Mannarino E; Annesi F; De Marco EV; Rocca FE; Greco V; Scornaienchi V; Tarantino P; Civitelli D; Quattrone A; Tortorella G; Annesi G. |