IRIS

ORLACCHIO, ANTONIO

ORLACCHIO, ANTONIO  

Dipartimento di Medicina dei sistemi  

Mostra records
Risultati 1 - 20 di 84 (tempo di esecuzione: 0.032 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-feb-1998 1H-MRS in patients with multiple sclerosis undergoing treatment with interferon beta-1a: results of a preliminary study Sarchielli, P; Presciutti, O; Tarducci, R; Gobbi, G; Alberti, A; Pelliccioli, G; Orlacchio, A; Gallai, V Articolo su rivista
15-nov-2013 A new CSF1R mutation presenting with an extensive white matter lesion mimicking primary progressive multiple sclerosis Inui, T; Kawarai, T; Fujita, K; Kawamura, K; Mitsui, T; Orlacchio, A; Kamada, M; Abe, T; Izumi, Y; Kaji, R Articolo su rivista
25-mag-2004 A new SPG4 mutation in a variant form of spastic paraplegia with congenital arachnoid cysts Orlacchio, A; Gaudiello, F; Totaro, A; Floris, R; St George Hyslop, P; Bernardi, G; Kawarai, T Articolo su rivista
1-lug-2007 A novel mutation in the SPG3A gene (atlastin) in hereditary spastic paraplegia Matsui, M; Kawarai, T; Hase, Y; Tomimoto, H; Iseki, K; Rogaeva, E; Orlacchio, A; Bernardi, G; St George Hyslop, P; Takahashi, R; Matsui, M Articolo su rivista
10-lug-1998 Absence of association between Alzheimer disease and the -491 regulatory region polymorphism of APOE Song, Y; Rogaeva, E; Premkumar, S; Brindle, N; Kawarai, T; Orlacchio, A; Yu, G; Levesque, G; Nishimura, M; Ikeda, M; Pei, Y; O'Toole, C; Duara, R; Barker, W; Sorbi, S; Freedman, M; Farrer, L; St George Hyslop, P Articolo su rivista
12-mag-2000 Absence of linkage between familial amyotrophic lateral sclerosis and copper chaperone for the superoxide dismutase gene locus in two Italian pedigrees Orlacchio, A; Kawarai, T; Massaro, A; St George Hyslop, P; Sorbi, S Articolo su rivista
1-dic-2005 Acanthocytosis as a predisposing factor non-ketotic hyperglycemia induced chorea-ballism Pisani, A; Diomedi, M; Rum, A; Cianciulli, P; Floris, R; Orlacchio, A; Bernardi, G; Calabresi, P Articolo su rivista
22-ott-1997 Activity levels of a beta1,6 N-acetylglucosaminyltransferase in lymphomonocytes from multiple sclerosis patients Orlacchio, A; Sarchielli, P; Gallai, V; Datti, A; Saccardi, C; Palmerini, C Articolo su rivista
15-ott-2005 AD with subcortical white matter lesions and vascular dementia: CSF markers for differential diagnosis Stefani, A; Bernardini, S; Panella, M; Pierantozzi, M; Nuccetelli, M; Koch, G; Urbani, A; Giordano, A; Martorana, A; Orlacchio, A; Federici, G; Bernardi, G Articolo su rivista
1-dic-2001 Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis Orlacchio, A; Bernardi, G; Orlacchio, A; Emiliani, C Articolo su rivista
1-gen-2002 Alpha-D-mannosidase properties in serum of patients with amyotrophic lateral sclerosis Orlacchio, A; Bernardi, G; Orlacchio, A; Emiliani, C Articolo su rivista
16-feb-2001 Alpha2-macroglobulin polymorphisms in Italian sporadic and familial Alzheimer's disease Nacmias, B; Tedde, A; Cellini, E; Forleo, P; Orlacchio, A; Guarnieri, B; Petruzzi, C; D'Andrea, F; Serio, A; Sorbi, S Articolo su rivista
1-mag-1999 An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease Rogaeva, E; Premkumar, S; Grubber, J; Serneels, L; Scott, W; Kawarai, T; Song, Y; Hill, D; Abou Donia, S; Martin, E; Vance, J; Yu, G; Orlacchio, A; Pei, Y; Nishimura, M; Supala, A; Roberge, B; Saunders, A; Roses, A; Schmechel, D; Crane Gatherum, A; Sorbi, S; Bruni, A; Small, G; Conneally, P; Haines, J; Van Leuven, F; St George Hyslop, P; Farrer, L; Pericak Vance, M Articolo su rivista
1-mag-2013 Application of long-range polymerase chain reaction in the diagnosis of X-linked dystonia-parkinsonism Kawarai, T; Pasco, P; Teleg, R; Kamada, M; Sakai, W; Shimozono, K; Mizuguchi, M; Tabuena, D; Orlacchio, A; Izumi, Y; Goto, S; Lee, L; Kaji, R Articolo su rivista
22-nov-2002 Association analysis between Alzheimer's disease and the Nicastrin gene polymorphisms Orlacchio, A; Kawarai, T; Polidoro, M; Stefani, A; Orlacchio, A; St George Hyslop, P; Bernardi, G Articolo su rivista
31-mag-2002 Association study of the 5-hydroxytryptamine(6) receptor gene in Alzheimer's disease Orlacchio, A; Kawarai, T; Paciotti, E; Stefani, A; Orlacchio, A; Sorbi, S; St George Hyslop, P; Bernardi, G Articolo su rivista
1-gen-2009 Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity Pippucci, T; Panza, E; Pompilii, E; Donadio, V; Borreca, A; Babalini, C; Patrono, C; Zuntini, R; Kawarai, T; Bernardi, G; Liguori, R; Romeo, G; Montagna, P; Orlacchio, A; Seri, M Articolo su rivista
1-dic-2000 beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I Beccari, T; Mancuso, F; Costanzi, E; Tassi, C; Barone, R; Fiumara, A; Orlacchio, A; Aisa, M; Orlacchio, A Articolo su rivista
1-set-1998 Beta-N-acetylhexosaminidase in peripheral blood lymphocytes and monocytes in the different forms and stages of multiple sclerosis Orlacchio, A; Martino, S; Sarchielli, P; Gallai, V; Emiliani, C Articolo su rivista
10-ott-2014 Bridging Over the Troubled Heterogeneity of SPG-Related Pathologies: Mechanisms Unite What Genetics Divide Tessa, A; Denora, P; Racis, L; Storti, E; Orlacchio, A; Santorelli, F Articolo su rivista