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Browsing by Author Breedveld, Guido J

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Issue DateTitleAuthor(s)
2007Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesisGrünewald, Anne; Breedveld, Guido J; Hedrich, Katja; Rohé, Christian F; König, Inke R; Hagenah, Johann; Vanacore, Nicola; Meco, Giuseppe; Antonini, Angelo; Goldwurm, Stefano; Lesage, Suzanne; Dürr, Alexandra; Binkofski, Ferdinand; Siebner, Hartwig; Münchau, Alexander; Brice, Alexis; Oostra, Ben A; Klein, Christine; Bonifati, Vincenzo
2006A common missense variant in the LRRK2 gene Gly2385Arg, associated with Parkinson's disease risk in TaiwanDi Fonzo, Alessio; Wu-Chou, Yah Huei; Lu, Chin Song; van Doeselaar, Marina; Simons, Erik J; Rohé, Christian F; Chang, Hsiu Chen; Chen, Rou Shayn; Weng, Yi Hsin; Vanacore, Nicola; Breedveld, Guido J; Oostra, Ben A; Bonifati, Vincenzo
2005Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's diseaseThe Italian Parkinson Genetics Network; Di Fonzo, Alessio; Tassorelli, Cristina; De Mari, Michele; Chien Hsin, F; Ferreira, Joachim; Rohé, Christian F; Riboldazzi, Giulo; Antonini, Angelo; Albani, Gianni; Mauro, Alessandro; Marconi, Roberto; Abruzzese, Giovanni; Lopiano, Leonardo; Fincati, Emilia; Guidi, Marco; Marini, Paolo; Stocchi, Fabrizio; Onofrj, Marco; Toni, Vincenzo; Tinazzi, Michele; Fabbrini, Giovanni; Lamberti, Paolo; Vanacore, Nicola; Meco, Giuseppe; Leitner, Petre; Uitti, Ryan J; Wszolek, Zbigniew K; Gasser, Thomas; Simons, Erik J; Breedveld, Guido J; Goldwurm, Stefano; Pezzoli, Gianni; Sampaio, Cristina; Barbosa, Egberto R; Martignoni, Elena; Oostra, Ben A; Bonifati, Vincenzo
2005Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesThe Italian Parkinson Genetics Network; Bonifati, Vincenzo; Rohé, Christian F; Breedveld, Guido J; Fabrizio, Edito; De Mari, Michele; Tassorelli, Carlo; Tavella, Alessandra; Marconi, Roberto; Nicholl, David; Chien Hsin, F; Fincati, Emilia; Abruzzese, Giovanni; Marini, Pietro; De Gaetano, A.; Horstink, M W; Maat-Kievit, J A; Sampaio, Cristina; Antonini, Angelo; Stocchi, Fabrizio; Montagna, Pasquale; Toni, Vincenzo; Guidi, Marco; Dalla Libera, Alessio; Tinazzi, Michele; De Pandis, Maria Francesca; Fabbrini, Giovanni; Goldwurm, Stefano; de Klein, A; Barbosa, Egberto R; Lopiano, Lorenzo; Martignoni, Elena; Lamberti, Paolo; Vanacore, Nicola; Meco, Giuseppe; Oostra, Ben A
2005A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's diseaseThe Italian Parkinson Genetics Network; Di Fonzo, Alessio; Rohé, Christian F; Ferreira, Joachim; Chien Hsin, F; Vacca, Laura; Stocchi, Fabrizio; Guedes, Leonor; Fabrizio, Edito; Manfredi, Mario; Vanacore, Nicola; Goldwurm, Stefano; Breedveld, Guido J; Sampaio, Cristina; Meco, Giuseppe; Barbosa, Egberto R; Oostra, Ben A; Bonifati, Vincenzo
2005The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorGoldwurm, Stefano; Di Fonzo, Alessio; Simons, Erik J; Rohé, Christian F; Zini, Michela; Canesi, Margherita; Tesei, Silvana; Zecchinelli, Anna; Antonini, Angelo; Mariani, Claudio; Meucci, Nicoletta; Sacilotto, Giorgio; Sironi, Francesca; Salani, Giuliana; Ferreira, Joachim; Chien Hsin, F; Fabrizio, Edito; Vanacore, Nicola; Dalla Libera, Alessio; Stocchi, Fabrizio; Diroma, Cosimo; Lamberti, Paolo; Sampaio, Cristina; Meco, Giuseppe; Barbosa, Egberto R; Bertoli-Avella, Aida M; Breedveld, Guido J; Oostra, Ben A; Pezzoli, Gianni; Bonifati, Vincenzo
2002Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismBonifati, Vincenzo; Rizzu, Patrizia; Van Baren, Marijke J; Schaap, Onno; Breedveld, Guido J; Krieger, Elmar; Dekker, Marieke C J; Squitieri, Ferdinando; Ibanez, Pablo; Joosse, Marijke; van Dongen, Jeroen W; Vanacore, Nicola; van Swieten, John C; Brice, Alexis; Meco, Giuseppe; van Duijn, Cornelia M; Oostra, Ben A; Heutink, Peter
Showing results 1 to 7 of 7

 

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