Authors:
Carrieri, G
Bonafe, M
De Luca, M
Rose, G
Varcasia, O
Bruni, A
Maletta, R
Nacmias, B
Sorbi, S
Corsonello, F
Feraco, E
Andreev, KF
Yashin, AI
Franceschi, C
De Benedictis, G
Citation: G. Carrieri et al., Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease, HUM GENET, 108(3), 2001, pp. 194-198
Authors:
Brunelli, T
Bagnoli, S
Giusti, B
Nacmias, B
Pepe, G
Sorbi, S
Abbate, R
Citation: T. Brunelli et al., The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease, NEUROSCI L, 315(1-2), 2001, pp. 103-105
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
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:
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:
Ballerini, C
Campani, D
Rambola, G
Gran, B
Nacmias, B
Amato, MP
Siracusa, G
Bartolozzi, L
Sorbi, S
Massacesi, L
Citation: C. Ballerini et al., Association of apolipoprotein E polymorphism to clinical heterogeneity of multiple sclerosis, NEUROSCI L, 296(2-3), 2000, pp. 174-176
Authors:
Balestrieri, M
Nacmias, B
Sorbi, S
Marcon, G
Citation: M. Balestrieri et al., Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation, PSYCHOTH PS, 69(6), 2000, pp. 335-338
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:
Brandi, ML
Becherini, L
Gennari, L
Racchi, M
Bianchetti, A
Nacmias, B
Sorbi, S
Mecocci, P
Senin, U
Govoni, S
Citation: Ml. Brandi et al., Association of the estrogen receptor alpha gene polymorphisms with sporadic Alzheimer's disease, BIOC BIOP R, 265(2), 1999, pp. 335-338