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Autor:
Cavanna, B, Carpo, M, Pedotti, R, Scarpini, E, Meucci, N, Allaria, S, Scarlato, G, Nobile-Orazio, E *
Publikováno v:
In Journal of Neuroimmunology 1999 94(1):157-164
Autor:
Healy, Daniel G., Mario, Falchi, O'Sullivan, Sean S., Bonifati, Vincenzo, Alexandra, Durr, Susan, Bressman, Alexis, Brice, Jan, Aasly, Zabetian, Cyrus P., Stefano, Goldwurm, Ferreira, Joaquim J., Eduardo, Tolosa, Kay, Denise M., Christine, Klein, Williams, David R., Connie, Marras, Lang, Anthony E., Wszolek, Zbigniew K., Jose, Berciano, Schapira, Anthony H. V., Timothy, Lynch, Bhatia, Kailash P., Thomas, Gasser, Lees, Andrew J., Wood, Nicholas W., International Lrrk Consortium, Collaborators, Tazir, M., Ysmail Dahlouk, F., Belarbi, S., Hecham, N., Barbosa, E., Chien, H. F., Rieder, C. R., Jardim, L. B., Rogaeva, E., Lesage, S., Lohmann, E., Vidailhet, M., Bonnet, A. M., Agid, Y., Pollak, P., Tison, F., Durif, F., Broussolle, E., Berg, D., Hagenah, J., Gosal, D., Gibson, M., Vanacore, Nicola, Berardelli, Alfredo, Fabbrini, Giovanni, Fabrizio, E., Meco, Giuseppe, Stocchi, F., Dalla Libera, A., De Mari, M., Lamberti, P., Cossu, G., Pezzoli, G., Zini, M., Tesei, S., Zecchinelli, A., Sironi, F., Antonini, A., Mariani, C., Sacilotto, G., Meucci, N., Canesi, M., Di Fonzo, A., Oostra, B., Correia Guedes, L., Rosa, Mm, Coelho, M., Sampaio, C., Gaig, C., C. S., Lu, Wu Chou, Y. H., Quinn, N. P., Abou Sleiman, P. M., Muqit, M. M., Khan, N. L., Gandhi, S., Vaughan, J., Payami, H., Nutt, J. J., Factor, S. A., Higgins, D. S., Farrer, M. J., Hulihan, M., Brown, L., Mata, I. F., Samii, A., Yearout, D., Griffith, A., Leis, B. C., Roberts, J. W.
Publikováno v:
Lancet Neurology, 7(7), 583-590. Lancet Publishing Group
The Lancet Neurology
The Lancet Neurology, 2008, 7 (7), pp.583-590
The Lancet Neurology, Elsevier, 2008, 7 (7), pp.583-590
The Lancet Neurology
The Lancet Neurology, 2008, 7 (7), pp.583-590
The Lancet Neurology, Elsevier, 2008, 7 (7), pp.583-590
Summary Background Mutations in LRRK2 , the gene that encodes leucine-rich repeat kinase 2, are a cause of Parkinson's disease (PD). The International LRRK2 Consortium was established to answer three key clinical questions: can LRRK2 -associated PD b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86cd088b2dcd94204ede5ac47e6f14f6
Autor:
Sharma, M, Wenning, G, Krüger, R, European Multiple-System Atrophy Study Group (Sharma, M, Lichtner, P, Albanese, Donatella, Barone, P, Berciano, J, Bloem, Br, Coelho, M, Goldwurm, S, Infante, J, Klockgether, T, Ortega-Cubero, S, Del Sorbo, F, Pezzoli, G, Canesi, M, Tesei, S, Zecchinelli, A, Sacilotto, G, Meucci, N, Mariani, C, Cilia, R, Zini, M, Siri, C, Pellecchia, Mt, Picillo, M, Amboni, M, Schulte, C, Martí, Mj, Sampaio, C, Ferreira, J, Levin, J, Nilsson, Cf, Widner, H, Østergaard, K, Oertel, W, Pastor, P, Storch, A, Seppi, K, Geser, F, Krismer, F, Mahlknecht, P, Sprenger, Fs, Schöls, L, Tolosa, E, Wüllner, U, van de Warrenburg BP, Poewe, W, Gasser, T, Krüger, R. ).
Publikováno v:
The New England journal of medicine 371(1), 80-83 (2014). doi:10.1056/NEJMc1311763
To the Editor: Tsuji and colleagues (July 18 issue)1 report that variants in the gene encoding coenzyme Q2 (COQ2) increase the risk of multiple-system atrophy. They observed homozygous COQ2 variants encoding the substitutions M78V and V343A in a cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b872d7d0bdd6e3c0eb5d9c8a06baaaf
http://hdl.handle.net/11386/4707172
http://hdl.handle.net/11386/4707172
Autor:
Sironi, F, Trotta, L, Antonini, A, Zini, M, Ciccone, R, DELLA MINA, E, Meucci, N, Sacilotto, G, Primignani, P, Brambilla, T, Coviello, Domenico, Pezzoli, G, Goldwurm, S.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3710::6722df6e679fc0b4b621399205786145
http://hdl.handle.net/11567/222715
http://hdl.handle.net/11567/222715