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Results: 1-11 |
Results: 11
Acute effects of bilateral subthalamic nucleus stimulation on clinical andkinematic parameters in Parkinson's disease
Authors: Carella, F Genitrini, S Bressanelli, M Soliveri, P Servello, D Broggi, G Piacentini, S Geminiami, G Girotti, F
Citation: F. Carella et al., Acute effects of bilateral subthalamic nucleus stimulation on clinical andkinematic parameters in Parkinson's disease, MOVEMENT D, 16(4), 2001, pp. 651-655
Clinical and genetic analysis of hereditary and sporadic ataxia in centralItaly
Authors: Cellini, E Forleo, P Nacmias, B Tedde, A Latorraca, S Piacentini, S Parnetti, L Gallai, V Sorbi, S
Citation: E. Cellini et al., Clinical and genetic analysis of hereditary and sporadic ataxia in centralItaly, BRAIN RES B, 56(3-4), 2001, pp. 363-366
Psychosis, serotonin receptor polymorphism and Alzheimer's disease
Authors: Nacmias, B Tedde, A Forleo, P Piacentini, S Latorraca, S Guarnieri, BM Ortenzi, L Bartoli, A Petruzzi, C Serio, A Sorbi, S
Citation: B. Nacmias et al., Psychosis, serotonin receptor polymorphism and Alzheimer's disease, ARCH GER G, 2001, pp. 279-283
Association between 5-HT2A receptor polymorphism and psychotic symptoms inAlzheimer's disease
Authors: Nacmias, B Tedde, A Forleo, P Piacentini, S Guarnieri, BM Bartoli, A Ortenzi, L Petruzzi, C Serio, A Marcon, G Sorbi, S
Citation: B. Nacmias et al., Association between 5-HT2A receptor polymorphism and psychotic symptoms inAlzheimer's disease, BIOL PSYCHI, 50(6), 2001, pp. 472-475
Association between 5-HT2A receptor polymorphism and psychotic symptoms inAlzheimer's disease (vol 50, pg 472, 2001)
Authors: Nacimas, B Tedde, A Forleo, P Piacentini, S Guarnieri, BM Bartoli, A Ortenzi, L Petruzzi, C Serio, A Marcon, G Sorbi, S
Citation: B. Nacimas et al., Association between 5-HT2A receptor polymorphism and psychotic symptoms inAlzheimer's disease (vol 50, pg 472, 2001), BIOL PSYCHI, 50(10), 2001, pp. 821-821
Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy
Authors: Cellini, E Nacmias, B Forleo, P Piacentini, S Guarnieri, BM Serio, A Calabro, A Renzi, D Sorbi, S
Citation: E. Cellini et al., Genetic and clinical analysis of spinocerebellar ataxia type 8 repeat expansion in Italy, ARCH NEUROL, 58(11), 2001, pp. 1856-1859
Guidelines for the diagnosis of dementia and Alzheimer's disease
Authors: Sorbi, S Alberoni, M Alfieri, P Vesuviana, S Amici, S Antana, D Appollonio, I Avanzi, S Bartoli, A Bergamasco, B Bracco, L Bruni, A Terme, L Bugiani, O Caffarra, P Caltagirone, C Carolei, A Casini, AR Ciannella, L Citterio, A Daniele, A D'Achille, G Del Curatolo, G Dell'Agnello, G Durante, D Farina, E Ferrero, P Forleo, P Gainotti, G Gabriele, P Galante, E Gallai, V Gallassi, R Gasparini, M Ghetti, B Giaccone, G Girotti, F Grimaldi, L Grioli, S Guarnieri, BM Grottoli, S Iemolo, F Latorraca, S Le Pira, F Lenzi, GL Lorusso, S Mariani, C Marcon, G Mascia, V Mearelli, S Morante, M Morbin, M Musicco, M Nardelli, E Nichelli, P Padovani, A Paganini, M Pantieri, R Parisen, P Parnetti, L Passerella, B Pettenati, C Piacentini, S Piccoli, F Piccolini, C Pizzolato, G Provinciali, L Pugliese, N Redi, F Ruggieri, RM Ruggiero, U Saetta, M Schoenuber, R Silveri, MC Sorbi, S Sorrentino, G Sucapane, P Stracciari, A Tabaton, M Tagliavini, F Toso, V Valluzzi, F
Citation: S. Sorbi et al., Guidelines for the diagnosis of dementia and Alzheimer's disease, NEUROL SCI, 21(4), 2000, pp. 187-194
Risperidone in idiopathic and symptomatic dystonia: preliminary experience
Authors: Grassi, E Latorraca, S Piacentini, S Marini, P Sorbi, S
Citation: E. Grassi et al., Risperidone in idiopathic and symptomatic dystonia: preliminary experience, NEUROL SCI, 21(2), 2000, pp. 121-123
Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia
Authors: Sorbi, S Forleo, P Fani, C Piacentini, S
Citation: S. Sorbi et al., Double-blind, crossover, placebo-controlled clinical trial with L-acetylcarnitine in patients with degenerative cerebellar ataxia, CLIN NEUROP, 23(2), 2000, pp. 114-118
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset
Authors: Tedde, A Forleo, P Nacmias, B Piccini, C Bracco, L Piacentini, S Sorbi, S
Citation: A. Tedde et al., A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset, NEUROLOGY, 55(10), 2000, pp. 1590-1591
Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat
Authors: Sorbi, S Forleo, P Cellini, E Piacentini, S Serio, A Guarnieri, B Petruzzi, C
Citation: S. Sorbi et al., Atypical Friedreich ataxia with a very late onset and an unusual limited GAA repeat, ARCH NEUROL, 57(9), 2000, pp. 1380-1381
Risultati: 1-11 |