SCALABRINI, DIEGO
SCALABRINI, DIEGO
Universita' degli Studi di MILANO
GSK3β genetic variability in patients with Multiple Sclerosis
2011 D. Galimberti, J. Macmurray, D. Scalabrini, C. Fenoglio, M.A. De Riz, C. Comi, D. Comings, F. Cortini, C. Villa, M. Serpente, C. Cantoni, E. Ridolfi, M.H. Fardipoor, M. Leone, F. Monaco, N. Bresolin, E.A. Scarpini
GRN variability contributes to sporadic frontotemporal lobar degeneration
2010 D. Galimberti, C. Fenoglio, F. Cortini, M. Serpente, E. Venturelli, C. Villa, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, D. Scalabrini, I. Restelli, F.M. Boneschi, S. Cappa, G. Binetti, C. Mariani, I. Rainero, M.T. Giordana, N. Bresolin, E. Scarpini
CHMP5 and BAG1 are protective factors for sporadic frontotemporal lobar degeneration
2010 D. Galimberti, C. Villa, E. Venturelli, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, D. Scalabrini, F. Cortini, M. Serpente, C. Cantoni, S. Cappa, G. Binetti, I. Rainero, M. Giordana, N. Bresolin, C. Mariani, E. Scarpini
Loss of epidermal growth factor regulation by cobalamin in multiple sclerosis
2010 G. Scalabrino, D. Galimberti, E. Mutti, D. Scalabrini, D. Veber, M. De Riz, F. Bamonti, E. Capello, G.L. Mancardi, E. Scarpini
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort
2010 F. Martinelli-Boneschi, F. Esposito, D. Scalabrini, C. Fenoglio, M.E. Rodegher, P. Brambilla, B. Colombo, A. Ghezzi, R. Capra, L. Collimedaglia, G. Coniglio, M. De Riz, M. Serpente, C. Cantoni, E. Scarpini, V. Martinelli, D. Galimberti, G. Comi G.
Is KIF24 a genetic risk factor for Frontotemporal Lobar degeneration?
2010 E. Venturelli, C. Villa, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, D. Scalabrini, F. Cortini, G. Fumagalli, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E. Scarpini, D. Galimberti
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males
2010 C. Fenoglio, D. Scalabrini, F. Esposito, C. Comi, P. Cavalla, M. De Riz, V. Martinelli, L.M. Piccio, E. Venturelli, G. Fumagalli, R. Capra, L. Collimedaglia, A. Ghezzi, M.E. Rodegher, M. Vercellino, M. Leone, M.T. Giordana, N. Bresolin, F. Monaco, G. Comi, E. Scarpini, F. Martinelli-Boneschi, D. Galimberti
Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes
2010 M.D. Riz, D. Galimberti, C. Fenoglio, L.M. Piccio, D. Scalabrini, E. Venturelli, A. Pietroboni, M. Piola, R.T. Naismith, B.J. Parks, G. Fumagalli, N. Bresolin, A.H. Cross, E. Scarpini
Candidate gene analysis of semaphorins in patients with Alzheimer's disease
2010 C. Villa, E. Venturelli, C. Fenoglio, M. De Riz, D. Scalabrini, F. Cortini, M. Serpente, C. Cantoni, N. Bresolin, E. Scarpini, D. Galimberti
Expression profile of miRNAs involved in CD4+ lymphocyte activation and differentiation in patients with multiple sclerosis
2010 D. Galimberti, C. Fenoglio, D. Scalabrini, M. Serpente, C. Cantoni, M. De Riz, L. Mellesi, S. Valzelli, A. Pietroboni, M. Piola, E. Venturelli, C. Villa, F. Cortini, N. Bresolin, E. Scarpini
Analisi genetica di molecole infiammatorie e di adesione coinvolte nella patogenesi della sclerosi multipla
2009 D. Scalabrini
rs 5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells from patients with Alzheimer's disease
2009 D. Galimberti, C. Fenoglio, F. Cortini, J.S.K. Kauwe, C. Cruchaga, E. Venturelli, D. Scalabrini, C. Villa, M. Serpente, K. Mayo, L.M. Piccio, F. Clerici, D. Albani, C. Mariani, G. Forloni, N. Bresolin, A.M. Goate, E.A. Scarpini
Progranulin gene variability in a population of 239 patients with primary progressive multiple sclerosis
2009 C. Fenoglio, F. Martinelli Boneschi, D. Galimberti, D. Scalabrini, F. Esposito, M. De Riz, L.M. Piccio, R. Naismith, B.J. Parks, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, F. Monaco, N. Bresolin, A.H. Cross, E. Scarpini
GRN rs5848 in neurodegeneration: a role in axonal damage?
2009 D. Scalabrini, C. Fenoglio, F. Martinelli, F. Boneschi, M. DE RIZ, F. Esposito, L. Piccio, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Piola, A. Pietroboni, N. Bresolin, A. Cross, D. Galimberti, E. Scarpini
CDKN2A and CDKN2B genetic variability in Alzheimer's disease patients.
2009 F. Cortini, C. Fenoglio, E. Venturelli, C. Villa, F. Clerici, D. Albani, D. Scalabrini, M. Serpente, C. Mariani, G. Forloni, N. Bresolin, E. Scarpini, D. Galimberti
GRN rs5848 polymorphism: a role in neurodegeneration?
2009 D. Scalabrini, C. Fenoglio, F. Martinelli Boneschi, M. De Riz, F. Esposito, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Piola, A. Pietroboni, N. Bresolin, D. Galimberti, E. Scarpini
MCP-1 A-2518G polymorphism: effect on sysceptibility for Frontotemporel Lobar Degeneration and on cerebrospina fluid MCP-1 levels.
2009 C. Villa, E. Venturelli, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, F. Cortini, D. Scalabrini, M. Serpente, I. Restelli, G. Binetti, S. Cappa, C. Mariani, N. Bresolin, E. Scarpini, D. Galimberti
KIF24 gene is associated with frontotemporal lobar degeneration.
2009 C. Villa, E. Venturelli, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, D. Scalabrini, G. Binetti, I. Rainero, M.T. Giordana, S. Cappa, C. Mariani, N. Bresolin, E. Scarpini, D. Galimberti
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for Frontotemporal Lobar Degeneration
2009 E. Venturelli, C. Villa, C. Fenoglio, F. Clerici, A. Marocne, R. Ghidoni, F. Cortini, D. Scalabrini, S. Gallone, I. Rainero, I. Restelli, M. Serpente, G. Binetti, S. Cappa, C. Mariani, M. Giordana, N. Bresolin, E. Scarpini, D. Galimberti
Progranulin genetic variability in primary progressive multiple sclerosis.
2009 C. Fenoglio, D. Galimberti, F. Martinelli-Boneschi, D. Scalabrini, F. Esposito, M. De Riz, L. Piccio, C. Comi, A. Pietroboni, M. Piola, E. Venturelli, F. Cortini, C. Villa, M. Serpente, M. Leone, N. Bresolin, A. Cross, G. Comi, E.A. Scarpini