Vincenzo Bonifati
AuthID: R-00F-EKF
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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; ...More
PUBLISHED: 2006, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 14, ISSUE: 3
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; ...More
PUBLISHED: 2006, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 14, ISSUE: 3
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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; ...More
PUBLISHED: 2005, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 42, ISSUE: 11
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; ...More
PUBLISHED: 2005, SOURCE: JOURNAL OF MEDICAL GENETICS, VOLUME: 42, ISSUE: 11
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TITLE: Early-onset parkinsonism associated with PINK1 mutations - Frequency, genotypes, and phenotypes
AUTHORS: Bonifati, V; Rohe, CF; Breedveld, GJ; Fabrizio, E; De Mari, M; Tassorelli, C; Tavella, A; Marconi, R; Nicholl, DJ; Chien, HF; Fincati, E; Abbruzzese, G; Marini, P; De Gaetano, A; Horstink, MW; Maat Kievit, JA; Sampaio, C; Antonini, A; Stocchi, F; Montagna, P; ...More
PUBLISHED: 2005, SOURCE: NEUROLOGY, VOLUME: 65, ISSUE: 1
AUTHORS: Bonifati, V; Rohe, CF; Breedveld, GJ; Fabrizio, E; De Mari, M; Tassorelli, C; Tavella, A; Marconi, R; Nicholl, DJ; Chien, HF; Fincati, E; Abbruzzese, G; Marini, P; De Gaetano, A; Horstink, MW; Maat Kievit, JA; Sampaio, C; Antonini, A; Stocchi, F; Montagna, P; ...More
PUBLISHED: 2005, SOURCE: NEUROLOGY, VOLUME: 65, ISSUE: 1
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TITLE: A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease Full Text
AUTHORS: Di Fonzo, A; Rohe, CF; Ferreira, RJ; Chien, HF; Vacca, L; Stocchi, F; Guedes, L; Fabrizio, E; Manfredi, M; Vanacore, N; Goldwurm, S; Breedveld, G; Sampaio, C; Meco, G; Barbosa, E; Oostra, BA; Bonifati, V;
PUBLISHED: 2005, SOURCE: LANCET, VOLUME: 365, ISSUE: 9457
AUTHORS: Di Fonzo, A; Rohe, CF; Ferreira, RJ; Chien, HF; Vacca, L; Stocchi, F; Guedes, L; Fabrizio, E; Manfredi, M; Vanacore, N; Goldwurm, S; Breedveld, G; Sampaio, C; Meco, G; Barbosa, E; Oostra, BA; Bonifati, V;
PUBLISHED: 2005, SOURCE: LANCET, VOLUME: 365, ISSUE: 9457
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TITLE: Exclusion of the Nurr1 gene in autosomal recessive Parkinson's disease Full Text
AUTHORS: Rawal, N; Periquet, M; Durr, A; de Michele, G; Bonifati, V; Teive, HA; Raskin, S; Guimaraes, J; Agid, Y; Brice, A;
PUBLISHED: 2002, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 249, ISSUE: 8
AUTHORS: Rawal, N; Periquet, M; Durr, A; de Michele, G; Bonifati, V; Teive, HA; Raskin, S; Guimaraes, J; Agid, Y; Brice, A;
PUBLISHED: 2002, SOURCE: JOURNAL OF NEUROLOGY, VOLUME: 249, ISSUE: 8
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