Independent and joint effects of the MAPT and SNCA genes in Parkinson disease von Elbaz, Alexis, Ross, Owen A., Ioannidis, John P. A., Soto-Ortolaza, Alexandra I., Moisan, Frédéric, Aasly, Jan, Annesi, Grazia, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Gibson, J. Mark, Gispert, Suzana, Hadjigeorgiou, Georgios M., Jasinska-Myga, Barbara, Klein, Christine, Krüger, Rejko, Lambert, Jean-Charles, Lohmann, Katja, van de Loo, Simone, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugénie, Nilsson, Christer, Opala, Grzegorz, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Stefanis, Leonidas, Uitti, Ryan J., Valente, Enza Maria, Vilariño-Güell, Carles, Wirdefeldt, Karin, Wszolek, Zbigniew K., Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J.

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β-Glucocerebrosidase gene mutations in two cohorts of Greek patients with sporadic Parkinson's disease von Moraitou, Marina, Hadjigeorgiou, Georgios, Monopolis, Ioannis, Dardiotis, Efthimios, Bozi, Maria, Vassilatis, Demitris, Vilageliu, Lluisa, Grinberg, Daniel, Xiromerisiou, Georgia, Stefanis, Leonidas, Michelakakis, Helen

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