C. Diroma


AuthID: R-00G-3M6

Publications Awaiting Confirmation

1
TITLE: ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
AUTHORS: Di Fonzo, A; Chien, HF; Socal, M; Giraudo, S; Tassorelli, C; Iliceto, G; Fabbrini, G; Marconi, R; Fincati, E; Abbruzzese, G; Marini, P; Squitieri, F; Horstink, MW; Montagna, P; Libera, AD; Stocchi, F; Goldwurm, S; Ferreira, JJ ; Meco, G; Martignoni, E; Lopiano, L; Jardim, LB; Oostra, BA; Barbosa, ER; Bonifati, V; Bonifati, V; Vanacore, N; Meco, G; Fabbrini, G; Fabrizio, E; Locuratolo, N; Scoppetta, C; Manfredi, M; Berardelli, A; Lopiano, L; Giraudo, S; Bergamasco, B; Tassorelli, C; Pacchetti, C; Nappi, G; Goldwurm, S; Antonini, A; Pezzoli, G; Riboldazzi, G; Bono, G; Raudino, F; Mi Manfredi; Fincati, E; Tinazzi, M; Bonizzato, A; Ferracci, C; Dalla Libera, A; Abbruzzese, G; Marchese, R; Montagna, P; Marini, P; Massaro, F; Marconi, R; Guidi, M; Minardi, C; Rasi, F; Onofrj, M; Thomas, A; Stocchi, F; Vacca, L; De Pandis, F; De Mari, M; Diroma, C; Iliceto, G; Lamberti, P; Toni, V; Trianni, G; Mauro, A; De Gaetano, A; Rizzo, M; Cossu, G; Rieder, CRM; Saraiva Pereira, ML; ...More
PUBLISHED: 2007, SOURCE: NEUROLOGY, VOLUME: 68, ISSUE: 19
INDEXED IN: Scopus WOS CrossRef
2
TITLE: Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease  Full Text
AUTHORS: Di Fonzo, A; Tassorelli, C; De Mari, M; Chien, HF; Ferreira, J ; Rohe, CF; Riboldazzi, G; Antonini, A; Albani, G; Mauro, A; Marconi, R; Abbruzzese, G; Lopiano, L; Fincati, E; Guidi, M; Marini, P; Stocchi, F; Onofrj, M; Toni, V; Tinazzi, M; Fabbrini, G; Lamberti, P; Vanacore, N; Meco, G; Leitner, P; Uitti, RJ; Wszolek, ZK; Gasser, T; Simons, EJ; Breedveld, GJ; Goldwurm, S; Pezzoli, G; Sampaio, C; Barbosa, E; Martignoni, E; Oostra, BA; Bonifati, V; Vancore, N; Fabrizio, E; Locuratolo, N; Martini, L; Scoppetta, C; Colosimo, C; Ma Manfredi; Lopiano, L; Tavella, A; Bergamasco, B; Tassorelli, C; Pacchetti, C; Nappi, G; Canesi, M; Calandrella, D; Brono, G; Mi Manfredi; Raudino, F; Corengia, E; Bonizzato, A; Ferracci, C; Dalla Libera, A; Marchese, R; Montagna, P; Ramat, S; Massaro, F; Minardi, C; Rasi, F; Thomas, A; Vacca, L; De Pandis, F; Diroma, C; Iliceto, G; Lamberti, P; Toni, V; Trianni, G; Mauro, A; De Gaetano, A; Rizzo, M; Cossu, G; ...More
PUBLISHED: 2006, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 14, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef
3
TITLE: The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor
AUTHORS: Goldwurm, S; Di Fonzo, A; Simons, EJ; Rohe, CF; Zini, M; Canesi, M; Tesei, S; Zecchinelli, A; Antonini, A; Mariani, C; Meucci, N; Sacilotto, G; Sironi, F; Salani, G; Ferreira, J ; Chien, HF; Fabrizio, E; Vanacore, N; Dalla Libera, A; Stocchi, F; Diroma, C; Lamberti, P; Sampaio, C; Meco, G; Barbosa, E; Bertoli Avella, AM; Breedveld, GJ; Oostra, BA; Pezzoli, G; Bonifati, V; ...More
PUBLISHED: 2005, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 42, ISSUE: 11
INDEXED IN: Scopus WOS CrossRef

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