1
TITLE: Gene Expression Differences in Peripheral Blood of Parkinson's Disease Patients with Distinct Progression Profiles  Full Text
AUTHORS: Raquel Pinho; Leonor C Guedes; Lilach Soreq; Patricia P Lobo; Tiago Mestre; Miguel Coelho; Mario M Rosa; Nilza Goncalves; Pauline Wales; Tiago Mendes; Ellen Gerhardt; Christiane Fahlbusch; Vincenzo Bonifati; Michael Bonin; Gabriel Miltenberger Miltenyi; Fran Borovecki; Hermona Soreq; Joaquim J Ferreira; Tiago F Outeiro;
PUBLISHED: 2016, SOURCE: PLOS ONE, VOLUME: 11, ISSUE: 6
INDEXED IN: WOS CrossRef
2
TITLE: EFNS/MDS-ES recommendations for the diagnosis of Parkinson's disease  Full Text
AUTHORS: Berardelli, A; Wenning, GK; Antonini, A; Berg, D; Bloem, BR; Bonifati, V; Brooks, D; Burn, DJ; Colosimo, C; Fanciulli, A; Ferreira, J; Gasser, T; Grandas, F; Kanovsky, P; Kostic, V; Kulisevsky, J; Oertel, W; Poewe, W; P Reese; Relja, M; Ruzicka, E; Schrag, A; Seppi, K; Taba, P; Vidailhet, M; ...More
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF NEUROLOGY, VOLUME: 20, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef
4
TITLE: Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review  Full Text
AUTHORS: Correia C Guedes; Ferreira, JJ ; Rosa, MM; Coelho, M; Bonifati, V; Sampaio, C;
PUBLISHED: 2010, SOURCE: PARKINSONISM & RELATED DISORDERS, VOLUME: 16, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef
5
TITLE: GIGYF2 mutations are not a frequent cause of familial Parkinson's disease  Full Text
AUTHORS: Di Fonzo, A; Fabrizio, E; Thomas, A; Fincati, E; Marconi, R; Tinazzi, M; Breedveld, GJ; Simons, EJ; Chien, HF; Ferreira, JJ ; Horstink, MW; Abbruzzese, G; Borroni, B; Cossu, G; Libera, AD; Fabbrini, G; Guidi, M; De Mari, M; Lopiano, L; Martignoni, E; Marini, P; Onofrj, M; Padovani, A; Stocchi, F; Toni, V; Sampaio, C; Barbosa, ER; Meco, G; Italian Parkinson Genetics Network The; Oostra, BA; Bonifati, V; ...More
PUBLISHED: 2009, SOURCE: PARKINSONISM & RELATED DISORDERS, VOLUME: 15, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef
6
TITLE: Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism  Full Text
AUTHORS: Owen A Ross; Cleanthe Spanaki; Alida Griffith; Chin Hsien Lin; Jennifer Kachergus; Kristoffer Haugarvoll; Helen Latsoudis; Andreas Plaitakis; Joaquim J Ferreira ; Cristina Sampaio; Vincenzo Bonifati; Ruey Meei Wu; Cyrus P Zabetian; Matthew J Farrer;
PUBLISHED: 2009, SOURCE: PARKINSONISM & RELATED DISORDERS, VOLUME: 15, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef
7
TITLE: Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study  Full Text
AUTHORS: Daniel G Healy; Mario Falchi; Sean S O'Sullivan; Vincenzo Bonifati; Alexandra Durr; Susan Bressman; Alexis Brice; Jan Aasly; Cyrus P Zabetian; Stefano Goldwurm; Joaquim J Ferreira ; Eduardo Tolosa; Denise M Kay; Christine Klein; David R Williams; Connie Marras; Anthony E Lang; Zbigniew KWszolek; Jose Berciano; Anthony H V Schapira; Timothy Lynch; Kailash P Bhatia; Thomas Gasser; Andrew J Lees; Nicholas W Wood; ...More
PUBLISHED: 2008, SOURCE: LANCET NEUROLOGY, VOLUME: 7, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef
8
TITLE: High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal  Full Text
AUTHORS: Joaquim J Ferreira ; Leonor Correia Guedes; Mario Miguel Rosa; Miguel Coelho; Marina van Doeselaar; Dorothea Schweiger; Alessio Di Fonzo; Ben A Oostra; Cristina Sampaio; Vincenzo Bonifati;
PUBLISHED: 2007, SOURCE: MOVEMENT DISORDERS, VOLUME: 22, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef
9
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
10
TITLE: Worldwide prevalence of Leucine-Rich repeat kinase 2 gene mutations in Parkinson's disease: A systematic review
AUTHORS: Guedes, LC; Ferreira, JJ; Rosa, MM; Coelho, M; Bonifati, V; Sampaio, C;
PUBLISHED: 2007, SOURCE: MOVEMENT DISORDERS, VOLUME: 22
INDEXED IN: WOS
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