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Results: 1-25 | 26-35
Results: 1-25/35
Which target for DBS in Parkinson's disease? Subthalamic nucleus versus globus pallidus internus
Authors: di Luzio, AES Ammannati, F Marini, P Sorbi, S Mennonna, P
Citation: Aes. Di Luzio et al., Which target for DBS in Parkinson's disease? Subthalamic nucleus versus globus pallidus internus, NEUROL SCI, 22(1), 2001, pp. 87-88
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
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease
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
Clinical and genetic analysis of an Italian family with Machado-Joseph disease
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
The C677T methylenetetrahydrofolate reductase mutation is not associated with Alzheimer's disease
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
alpha 2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease
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
Spontaneous and induced chromosome damage in somatic cells of sporadic andfamilial Alzheimer's disease patients
Authors: Trippi, F Botto, N Scarpato, R Petrozzi, L Bonuccelli, U Latorraca, S Sorbi, S Migliore, L
Citation: F. Trippi et al., Spontaneous and induced chromosome damage in somatic cells of sporadic andfamilial Alzheimer's disease patients, MUTAGENESIS, 16(4), 2001, pp. 323-327
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
Genetic risk factors in familial Alzheimer's disease
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
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
Cognitive dysfunction in early-onset multiple sclerosis - A reappraisal after 10 years
Authors: Amato, MP Ponziani, G Siracusa, G Sorbi, S
Citation: Mp. Amato et al., Cognitive dysfunction in early-onset multiple sclerosis - A reappraisal after 10 years, ARCH NEUROL, 58(10), 2001, pp. 1602-1606
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
Music and cerebral hemodynamics
Authors: Marinoni, M Grassi, E Latorraca, S Caruso, A Sorbi, S
Citation: M. Marinoni et al., Music and cerebral hemodynamics, J CL NEUROS, 7(5), 2000, pp. 425-428
Association of early-onset disease with an Alzheimer's disease with an interleukin-1 alpha gene polymorphism
Authors: Grimaldi, LME Casadei, VM Ferri, C Veglia, F Licastro, F Annoni, G Biunno, I De Bellis, G Sorbi, S Mariani, C Canal, N Griffin, WST Franceschi, M
Citation: Lme. Grimaldi et al., Association of early-onset disease with an Alzheimer's disease with an interleukin-1 alpha gene polymorphism, ANN NEUROL, 47(3), 2000, pp. 361-365
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
Phospholipid composition and levels are not altered in fibroblasts bearingpresenilin-1 mutations
Authors: Murphy, EJ Zhang, H Sorbi, S Rapoport, SI Gibson, GE
Citation: Ej. Murphy et al., Phospholipid composition and levels are not altered in fibroblasts bearingpresenilin-1 mutations, BRAIN RES B, 52(3), 2000, pp. 207-212
Association of apolipoprotein E polymorphism to clinical heterogeneity of multiple sclerosis
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
Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis
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
Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees
Authors: Orlacchio, A Kawarai, T Massaro, AM St George-Hyslop, PH Sorbi, S
Citation: A. Orlacchio et al., Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees, NEUROSCI L, 285(2), 2000, pp. 83-86
Are premorbid personality traits linked to the risk of Alzheimer's disease? A case series of subjects with familial mutation
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
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
Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and beta APP processing
Authors: Yu, G Nishimura, M Arawaka, S Levitan, D Zhang, LL Tandon, A Song, YQ Rogaeva, E Chen, FS Kawaral, T Supala, A Levesque, L Yu, H Yang, DS Holmes, E Millman, P Liang, Y Zhang, DM Xu, DH Sato, C Rogaev, E Smith, M Janus, C Zhang, YN Aebersold, R Farrer, L Sorbi, S Bruni, A Fraser, P St George-Hyslop, P
Citation: G. Yu et al., Nicastrin modulates presenilin-mediated notch/glp-1 signal transduction and beta APP processing, NATURE, 407(6800), 2000, pp. 48-54
Risultati: 1-25 | 26-35