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Results:
1-9
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Results: 9
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:
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:
Gestri, D
Cecchi, C
Tedde, A
Latorraca, S
Orlacchio, A
Grassi, E
Massaro, AM
Liguri, G
St George-Hyslop, PH
Sorbi, S
Citation: D. Gestri et al., Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis, NEUROSCI L, 289(3), 2000, pp. 157-160
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:
Nacmias, B
Ricca, V
Tedde, A
Mezzani, B
Rotella, CM
Sorbi, S
Citation: B. Nacmias et al., 5-HT2A receptor gene polymorphisms in anorexia nervosa and bulimia nervosa, NEUROSCI L, 277(2), 1999, pp. 134-136
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