FRIGERIO, ROBERTA
FRIGERIO, ROBERTA
DIPARTIMENTO DI CHIRURGIA E MEDICINA INTERDISCIPLINARE (attivo dal 01/10/2012 al 31/10/2013)
Using global team science to identify genetic parkinson's disease worldwide
2019 Vollstedt, E; Kasten, M; Klein, C; Aasly, J; Adler, C; Ahmad-Annuar, A; Albanese, A; Alcalay, R; Al-Mubarak, B; Alvarez, V; Andree-Munoz, B; Annesi, G; Appel-Cresswell, S; Arkadir, D; Armasu, S; Barber, T; Bardien, S; Barkhuizen, M; Barrett, M; Basak, A; Beach, T; Benitez, B; Berg, D; Bhatia, K; Binkofski, F; Blauwendraat, C; Bonifati, V; Borges, V; Bozi, M; Brice, A; Brighina, L; Brockmann, K; Brucke, T; Bruggemann, N; Camacho, M; Cardoso, F; Belin, A; Carr, J; Chan, P; Chang-Castello, J; Chase, B; Chen-Plotkin, A; Ju Chung, S; Cilia, R; Clarimon, J; Clark, L; Cornejo-Olivas, M; Corvol, J; Cosentino, C; Cras, P; Crosiers, D; Damasio, J; Das, P; de Carvalho Aguiar, P; De Michele, G; De Rosa, A; Dieguez, E; Dorszewska, J; Erer, S; Ertan, S; Farrer, M; Fedotova, E; Ferese, R; Ferrarese, C; Ferraz, H; Fiala, O; Foroud, T; Friedman, A; Frigerio, R; Funayama, M; Gambardella, S; Garraux, G; Gatto, E; Genc, G; Giladi, N; Goldwurm, S; Gomez-Esteban, J; Gomez-Garre, P; Gorostidi, A; Grosset, D; Hanagasi, H; Hardy, J; Hassan, A; Hattori, N; Hauser, R; Hedera, P; Hentati, F; Hertz, J; Holton, J; Houlden, H; Hutz, M; Ikeuchi, T; Illarioshkin, S; Inca-Martinez, M; Infante, J; Jankovic, J; Jeon, B; Jesus, S; Jimenez-Del-Rio, M; Kaasinen, V; Kasten, M; Kataoka, H; Kawakami, H; Kim, Y; Klein, C; Klivenyi, P; Koks, S; Konig, I; Kostic, V; Koziorowski, D; Kruger, R; Krygowska-Wajs, A; Kulisevsky, J; Lai, D; Lang, A; Ledoux, M; Lesage, S; Lim, S; Lin, C; Lohmann, K; Lopera, F; Lopez, G; Lu, C; Lynch, T; Machaczka, M; Madoev, H; Magalhaes, M; Majamaa, K; Maraganore, D; Marder, K; Markopoulou, K; Martikainen, M; Mata, I; Mazzetti, P; Mellick, G; Menendez-Gonzalez, M; Micheli, F; Mirelman, A; Mir, P; Morino, H; Morris, H; Munhoz, R; Naito, A; Olszewska, D; Ozelius, L; Padmanabhan, S; Paisan-Ruiz, C; Payami, H; Peluso, S; Petkovic, S; Petrucci, S; Pezzoli, G; Pimentel, M; Pirker, W; Pramstaller, P; Pulkes, T; Puschmann, A; Quattrone, A; Raggio, V; Ransmayr, G; Rieder, C; Riess, O; Rodriguez-Porcel, F; Rogaeva, E; Ross, O; Ruiz-Martinez, J; Sammler, E; San Luciano, M; Satake, W; Saunders-Pullman, R; Sazci, A; Scherzer, C; Schrag, A; Schumacher-Schuh, A; Sharma, M; Sidransky, E; Singleton, A; Petersen, M; Smolders, S; Spitz, M; Stefanis, L; Struhal, W; Sue, C; Swan, M; Swanberg, M; Taba, P; Taipa, R; Tan, M; Tan, A; Tan, E; Tang, B; Tayebi, N; Thaler, A; Thomas, A; Toda, T; Toft, M; Torres, L; Tumas, V; Valente, E; Van Broeckhoven, C; Vecsei, L; Velez-Pardo, C; Vidailhet, M; Vollstedt, E; Warner, T; Williams-Gray, C; Winkelmann, J; Woitalla, D; Wood, N; Wszolek, Z; Wu, R; Wu, Y; Xie, T; Yoshino, H; Zhang, B; Zimprich, A
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy
2004 Frigerio, R; Fabrizi, G; Ferrarini, M; Cavallaro, T; Brighina, L; Santoro, P; Agostoni, E; Cavaletti, G; Rizzuto, N; Ferrarese, C
Titolo | Tipologia | Data di pubblicazione | Autori | File |
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Using global team science to identify genetic parkinson's disease worldwide | 01 - Articolo su rivista | 2019 | Brighina L.Camacho M.Cilia R.De Rosa A.Ferrarese C.Frigerio R.Peluso S.Petrucci S. + | |
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy | 01 - Articolo su rivista | 2004 | FRIGERIO, ROBERTABRIGHINA, LAURACAVALETTI, GUIDO ANGELOFERRARESE, CARLO + |