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Results:
1-12
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Results: 12
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
Authors:
Forleo, P
Cellini, E
Parnetti, L
Murasecco, D
Gallai, V
Nacmias, B
Sorbi, S
Citation: P. Forleo et al., Clinical and genetic analysis of an Italian family with Machado-Joseph disease, J NEUROL, 248(8), 2001, pp. 717-719
Authors:
Nacmias, B
Tedde, A
Cellini, E
Forleo, P
Orlacchio, A
Guarnieri, BM
Petruzzi, C
D'Andrea, F
Serio, A
Sorbi, S
Citation: B. Nacmias et al., alpha 2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease, NEUROSCI L, 299(1-2), 2001, pp. 9-12
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
Authors:
Sorbi, S
Forleo, P
Tedde, A
Cellini, E
Ciantelli, M
Bagnoli, S
Nacmias, B
Citation: S. Sorbi et al., Genetic risk factors in familial Alzheimer's disease, MECH AGE D, 122(16), 2001, pp. 1951-1960
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
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
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
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
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
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
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
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