SORBI, SANDRO

SORBI, SANDRO  

Neuroscienze, Area del Farmaco e Salute del Bambino (NEUROFARBA)  

Mostra records
Risultati 1 - 20 di 585 (tempo di esecuzione: 0.025 secondi).
Titolo Data di pubblicazione Autore(i) File
"Alpha2 macroglobulin and Alzheimer's disease" 1999 ROGAEVA E.; S. SORBI; ST GEORGE-HYSLOP P.H.; FARRR L.A; PERICAK-VANCE M.A
"Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity" 1998 ROGAEVA E; PREMKUMAR S.; SONG Y.S.; S. SORBI; BRINDLE N
"stato dell'arte" della ricerca 2012 Sorbi S; Bagnoli S; Piaceri I; Ferrari C; Lombardi G; Nacmias B
5-HT2A promoter polymorphism in anorexia nervosa. 1998 S. Sorbi; B. Nacmias; A. Tedde; V. Ricca; B. Mezzani; C. M. Rotella
5-HT2A receptor gene polymorphism and eating disorders. 2002 Ricca V; Nacmias B; Cellini E; Di Bernardo M; Rotella CM; Sorbi S.
5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa 1999 Nacmias B; Ricca V; Tedde A; Mezzani B; Rotella CM; Sorbi S.
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers 2018 Zhang, Ming; Ferrari, Raffaele; Tartaglia, Maria Carmela; Keith, Julia; Surace, Ezequiel I; Wolf, Uri; Sato, Christine; Grinberg, Mark; Liang, Yan; Xi, Zhengrui; Dupont, Kyle; McGoldrick, Philip; Weichert, Anna; McKeever, Paul M; Schneider, Raphael; McCorkindale, Michael D; Manzoni, Claudia; Rademakers, Rosa; Graff-Radford, Neill R; Dickson, Dennis W; Parisi, Joseph E; Boeve, Bradley F; Petersen, Ronald C; Miller, Bruce L; Seeley, William W; van Swieten, John C; van Rooij, Jeroen; Pijnenburg, Yolande; van der Zee, Julie; Van Broeckhoven, Christine; Le Ber, Isabelle; Van Deerlin, Vivianna; Suh, EunRan; Rohrer, Jonathan D; Mead, Simon; Graff, Caroline; Öijerstedt, Linn; Pickering-Brown, Stuart; Rollinson, Sara; Rossi, Giacomina; Tagliavini, Fabrizio; Brooks, William S; Dobson-Stone, Carol; Halliday, Glenda M; Hodges, John R; Piguet, Olivier; Binetti, Giuliano; Benussi, Luisa; Ghidoni, Roberta; Nacmias, Benedetta; Sorbi, Sandro; Bruni, Amalia C; Galimberti, Daniela; Scarpini, Elio; Rainero, Innocenzo; Rubino, Elisa; Clarimon, Jordi; Lleó, Alberto; Ruiz, Agustin; Hernández, Isabel; Pastor, Pau; Diez-Fairen, Monica; Borroni, Barbara; Pasquier, Florence; Deramecourt, Vincent; Lebouvier, Thibaud; Perneczky, Robert; Diehl-Schmid, Janine; Grafman, Jordan; Huey, Edward D; Mayeux, Richard; Nalls, Michael A; Hernandez, Dena; Singleton, Andrew; Momeni, Parastoo; Zeng, Zhen; Hardy, John; Robertson, Janice; Zinman, Lorne; Rogaeva, Ekaterina
A case of limbic encephalitis evolving into a frontotemporal dementia-like picture 2019 Lombardi G.; Mata S.; Berti V.; Padiglioni S.; Ginestroni A.; Piaceri I.; Bagnoli S.; Nacmias B.; De Cristofaro M.T.; Pupi A.; Sorbi S.
A comparison of unawareness in frontotemporal dementia and Alzheimer's disease. 2008 E. Salmon; D. Perani; F. Collette; D. Feyers; E. Kalbe; V. Holthoff; S. Sorbi; K. Herholz
A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia. 2002 Elena Cellini; Silvia Piacentini; Benedetta Nacmias; Paolo Forleo; Andrea Tedde; Silvia Bagnoli; Monica Ciantelli; Sandro Sorbi
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 2014 Fogh, I; Ratti, A; Gelleram, C; Lin, K; Tiloca, C; Moskvina, V; Corrado, L; Sorarù, G; Cereda, C; Corti, S; Gentilini, D; Calini, D; Castellotti, B; Mazzini, L; Querin, G; Gagliardi, S; Del Bo, R; Conforti, FL; Siciliano, G; Inghilleri, M; Saccà, F; Bongioanni, P; Penco, S; Corbo, M; Sorbi, S; Filosto, M; Ferlini, A; Di Blasio, AM; Signorini, S; Shatunov, A; Jones, A; Shaw, PJ; Morrison, KE; Farmer, AE; Van Damme, P; Robberecht, W; Chiò, A; Traynor, BJ; Sendtner, M; Melki, J; Meininger, V; Hardiman, O; Andersen, PM; Leigh, NP; Glass, JD; Overste, D; Diekstra, FP; Veldink, JH; van Es, MA; Shaw, CE; Weale, ME; Lewis, CM; Williams, J; Brown, RH; Landers, JE; Ticozzi, N; Ceroni, M; Pegoraro, E; Comi, GP; D'Alfonso, S; van den Berg, LH; Taroni, F; Al-Chalabi, A; Powell, J; Silani, V; the SLAGEN Consortium and Collaborators
A new paraplegin mutation in a patient with primary progressive multiple sclerosis 2020 Bellinvia A.; Pasto L.; Niccolai C.; Tessa A.; Carrai R.; Martinelli C.; Moretti M.; Amato M.P.; Santorelli F.M.; Sorbi S.; Mata S.
A new social-family model for eating disorders: A European multicentre project using a case-control design 2015 Krug, Isabel; Fuller-Tyszkiewicz, Matthew; Anderluh, Marija; Bellodi, Laura; Bagnoli, Silvia; Collier, David; Fernandez-Aranda, Fernando; Karwautz, Andreas; Mitchell, Sarah; Nacmias, Benedetta; Ricca, Valdo; Sorbi, Sandro; Tchanuria, Kate; Wagner, Gudrun; Treasure, Janet; Micali, Nadia
A novel Alzheimer disease locus located near the gene encoding tau protein 2016 Jun, G; Ibrahim-Verbaas, C A; Vronskaya, M; Lambert, J-C; Chung, J; Naj, A C; Kunkle, B W; Wang, L-S; Bis, J C; Bellenguez, C; Harold, D; Lunetta, K L; Destefano, A L; Grenier-Boley, B; Sims, R; Beecham, G W; Smith, A V; Chouraki, V; Hamilton-Nelson, K L; Ikram, M A; Fievet, N; Denning, N; Martin, E R; Schmidt, H; Kamatani, Y; Dunstan, M L; Valladares, O; Laza, A R; Zelenika, D; Ramirez, A; Foroud, T M; Choi, S-H; Boland, A; Becker, T; Kukull, W A; van der Lee, S J; Pasquier, F; Cruchaga, C; Beekly, D; Fitzpatrick, A L; Hanon, O; Gill, M; Barber, R; Gudnason, V; Campion, D; Love, S; Bennett, D A; Amin, N; Berr, C; Tsolaki, Magda; Buxbaum, J D; Lopez, O L; Deramecourt, V; Fox, N C; Cantwell, L B; Tárraga, L; Dufouil, C; Hardy, J; Crane, P K; Eiriksdottir, G; Hannequin, D; Clarke, R; Evans, D; Mosley, T H; Letenneur, L; Brayne, C; Maier, W; De Jager, P; Emilsson, V; Dartigues, J-F; Hampel, H; Kamboh, M I; de Bruijn, R F A G; Tzourio, C; Pastor, P; Larson, E B; Rotter, J I; O'Donovan, M C; Montine, T J; Nalls, M A; Mead, S; Reiman, E M; Jonsson, P V; Holmes, C; St George-Hyslop, P H; Boada, M; Passmore, P; Wendland, J R; Schmidt, R; Morgan, K; Winslow, A R; Powell, J F; Carasquillo, M; Younkin, S G; Jakobsdóttir, J; Kauwe, J S K; Wilhelmsen, K C; Rujescu, D; Nöthen, M M; Hofman, A; Jones, L; Haines, J L; Psaty, B M; Van Broeckhoven, C; Holmans, P; Launer, L J; Mayeux, R; Sorbi, S; Nacmias, B; Lathrop, M; Goate, A M; Escott-Price, V; Seshadri, S; Pericak-Vance, M A; Amouyel, P; Williams, J; van Duijn, C M; Schellenberg, G D; Farrer, L A
A novel but non-pathogenic mutation in exon 4 of the human amyloid precursor protein (APP) gene 1992 Vaula G.; Mortilla M.; Tupler R.; Lukiw W.; Tanzi R.; Nee L.; Polinsky R.; Foncin J.-F.; Bruni A.C.; Montesi M.P.; Sorbi S.; St George-Hyslop P.
A novel PS-1 mutation in an Italian AD family with psychotic symptoms at onset 2000 Tedde A.; Nacmias B.; Forleo P.; Piccini C.; Bracco L.; Piacentini S.; Sorbi S.
A Pan-European study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability and Intermediate Repeats 2013 van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Theuns J, Philtjens S, Sleegers K, Bäumer V, Maes G, Corsmit E, Cruts M, Van Broeckhoven C, van der Zee J, Gijselinck I, Dillen L, Van Langenhove T, Philtjens S, Theuns J, Sleegers K, Bäumer V, Maes G, Cruts M, Van Broeckhoven C, Engelborghs S, De Deyn PP, Cras P, Engelborghs S, De Deyn PP, Vandenbulcke M, Vandenbulcke M, Borroni B, Padovani A, Archetti S, Perneczky R, Diehl-Schmid J, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Synofzik M, Maetzler W, Müller Vom Hagen J, Schöls L, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, de Mendonça A, Miltenberger-Miltenyi G, Pereira S, Firmo C, Pimentel J, Sanchez-Valle R, Llado A, Antonell A, Molinuevo J, Gelpi E, Graff C, Chiang HH, Westerlund M, Graff C, Kinhult Ståhlbom A, Thonberg H, Nennesmo I, Börjesson-Hanson A, Nacmias B, Bagnoli S, Sorbi S, Bessi V, Piaceri I, Santana I, Santiago B, Santana I, Helena Ribeiro M, Rosário Almeida M, Oliveira C, Massano J, Garret C, Pires P, Frisoni G, Zanetti O, Bonvicini C, Sarafov S, Tournev I, Jordanova A, Tournev I, Kovacs GG, Ströbel T, Heneka MT, Jessen F, Ramirez A, Kurzwelly D, Sachtleben C, Mairer W, Jessen F, Matej R, Parobkova E, Danel A, Arzberger T, Maria Fabrizi G, Testi S, Ferrari S, Cavallaro T, Salmon E, Santens P, Cras P
A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study 2021 Bergström, Sofia; Öijerstedt, Linn; Remnestål, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D; Sorbi, Sandro; Nacmias, Benedetta; Månberg, Anna; Graff, Caroline; Nilsson, Peter; Ferrari, Camilla
A Pilot Study Evaluating the Contribution of SLC19A1 (RFC-1) 80G>A Polymorphism to Alzheimer’s Disease in Italian Caucasians 2014 Fabio Coppedè;Pierpaola Tannorella;Gloria Tognoni;Silvia Bagnoli;Paolo Bongioanni;Benedetta Nacmias;Gabriele Siciliano;Sandro Sorbi;Ubaldo Bonuccelli;Lucia Migliore
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset. 2000 TEDDE A; FORLEO P; NACMIAS B; PICCINI C; BRACCO L; PIACENTINI S; S. SORBI