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Results:
1-14
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Results: 14
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:
Beccari, T
Balducci, C
Aisa, MC
Della Fazia, MA
Servillo, G
Orlacchio, A
Citation: T. Beccari et al., Promoter characterization and expression of the gene coding for the human GM2 activator protein, BIOSCI REP, 21(1), 2001, pp. 55-62
Authors:
Nocentini, U
Rossini, PM
Carlesimo, GA
Graceffa, A
Grasso, MG
Lupoi, D
Oliveri, M
Orlacchio, A
Pozzilli, C
Rizzato, B
Caltagirone, C
Citation: U. Nocentini et al., Patterns of cognitive impairment in secondary progressive stable phase of multiple sclerosis: Correlations with MRI findings, EUR NEUROL, 45(1), 2001, pp. 11-18
Authors:
Costanzi, E
Beccari, T
Stinchi, S
Bibi, L
Hopwood, JJ
Orlacchio, A
Citation: E. Costanzi et al., Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mapping, MAMM GENOME, 11(6), 2000, pp. 436-439
Authors:
Ciferri, S
Emiliani, C
Guglielmini, G
Orlacchio, A
Nenci, GG
Gresele, P
Citation: S. Ciferri et al., Platelets release their lysomal content in vivo in humans upon activation, THROMB HAEM, 83(1), 2000, pp. 157-164
Authors:
Tancini, B
Emiliani, C
Mencarelli, S
Cavalieri, C
Stirling, JL
Orlacchio, A
Citation: B. Tancini et al., Evidence for the regulation of beta-N-acetylhexosaminidase expression during pregnancy in the rat, BBA-GEN SUB, 1475(2), 2000, pp. 184-190
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:
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
Authors:
Beccari, T
Mancuso, F
Costanzi, E
Tassi, C
Barone, R
Fiumara, A
Orlacchio, A
Aisa, MC
Orlacchio, A
Citation: T. Beccari et al., beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I, CLIN CHIM A, 302(1-2), 2000, pp. 125-132
Authors:
Devi, G
Fotiou, A
Jyrinji, D
Tycko, B
DeArmand, S
Rogaeva, E
Song, YQ
Medieros, H
Liang, Y
Orlacchio, A
Williamson, J
St George-Hyslop, P
Mayeux, R
Citation: G. Devi et al., Novel presenilin 1 mutations associated with early onset of dementia in a family with both early-onset and late-onset Alzheimer disease, ARCH NEUROL, 57(10), 2000, pp. 1454-1457
Authors:
Rogaeva, EA
Premkumar, S
Grubber, J
Serneels, L
Scott, WK
Kawarai, T
Song, YQ
Hill, DM
Abou-Donia, SM
Martin, ER
Vance, JJ
Yu, G
Orlacchio, A
Pei, Y
Nishimura, M
Supala, A
Roberge, B
Saunders, AM
Roses, AD
Schmechel, D
Crane-Gatherum, A
Sorbi, S
Bruni, A
Small, GW
Conneally, PM
Haines, JL
Van Leuven, F
St George-Hyslop, PH
Farrer, LA
Pericak-Vance, MA
Citation: Ea. Rogaeva et al., An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease, NAT GENET, 22(1), 1999, pp. 19-21
Authors:
Stinchi, S
Lullmann-Rauch, R
Hartmann, D
Coenen, R
Beccari, T
Orlacchio, A
von Figura, K
Saftig, P
Citation: S. Stinchi et al., Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis, HUM MOL GEN, 8(8), 1999, pp. 1365-1372
Authors:
Beccari, T
Stinchi, S
Orlacchio, A
Citation: T. Beccari et al., Lysosomal alpha 3-D-mannosidase, BIOSCI REP, 19(3), 1999, pp. 157-162
Authors:
Costanzi, E
Beccari, T
Tassi, C
Orlacchio, A
Rossi, A
Citation: E. Costanzi et al., Elevated beta-N-acetylhexosaminidase activity in focal dystonia fibroblasts, CLIN CHIM A, 288(1-2), 1999, pp. 31-35
Risultati:
1-14
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