VILLA, CHIARA
VILLA, CHIARA
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis
2007 Scalabrini, D; Fenoglio, C; Scarpini, E; De Riz, M; Comi, C; Venturelli, E; Cortini, F; Piola, M; Villa, C; Naldi, P; Monaco, F; Bresolin, N; Galimberti, D
Novel exon 1 progranulin gene variant in Alzheimer's disease
2008 Cortini, F; Fenoglio, C; Guidi, I; Venturelli, E; Pomati, S; Marcone, A; Scalabrini, D; Villa, C; Clerici, F; Dalla Valle, E; Mariani, C; Cappa, S; Bresolin, N; Scarpini, E; Galimberti, D
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration
2008 Venturelli, E; Villa, C; Scarpini, E; Fenoglio, C; Guidi, I; Lovati, C; Marcone, A; Cortini, F; Scalabrini, D; Clerici, F; Bresolin, N; Mariani, C; Cappa, S; Galimberti, D
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration
2008 Galimberti, D; Venturelli, E; Fenoglio, C; Guidi, I; Villa, C; Bergamaschini, L; Cortini, F; Scalabrini, D; Baron, P; Vergani, C; Bresolin, N; Scarpini, E
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
2009 Venturelli, E; Villa, C; Fenoglio, C; Clerici, F; Marcone, A; Ghidoni, R; Cortini, F; Scalabrini, D; Gallone, S; Rainero, I; Mandelli, A; Restelli, I; Binetti, G; Cappa, S; Mariani, C; Giordana, M; Bresolin, N; Scarpini, E; Galimberti, D
Candidate gene analysis of selectin cluster in patients with multiple sclerosis
2009 Fenoglio, C; Scalabrini, D; Piccio, L; De Riz, M; Venturelli, E; Cortini, F; Villa, C; Serpente, M; Parks, B; Rinker, J; Cross, A; Bresolin, N; Scarpini, E; Galimberti, D
MCP-1 A-2518G polymorphism: Effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels
2009 Galimberti, D; Venturelli, E; Villa, C; Fenoglio, C; Clerici, F; Marcone, A; Benussi, L; Cortini, F; Scalabrini, D; Perini, L; Restelli, I; Binetti, G; Cappa, S; Mariani, C; Bresolin, N; Scarpini, E
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
2009 Villa, C; Venturelli, E; Fenoglio, C; Clerici, F; Marcone, A; Benussi, L; Gallone, S; Scalabrini, D; Cortini, F; Serpente, M; Martinelli Boneschi, F; Cappa, S; Binetti, G; Mariani, C; Rainero, I; Giordana, M; Bresolin, N; Scarpini, E; Galimberti, D
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration
2009 Villa, C; Venturelli, E; Fenoglio, C; Clerici, F; Marcone, A; Benussi, L; Ghidoni, R; Gallone, S; Cortini, F; Scalabrini, D; Serpente, M; Binetti, G; Cappa, S; Mariani, C; Rainero, I; Bresolin, N; Scarpini, E; Galimberti, D
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with alzheimer's disease
2009 Fenoglio, C; Galimberti, D; Cortini, F; Kauwe, J; Cruchaga, C; Venturelli, E; Villa, C; Serpente, M; Scalabrini, D; Mayo, K; Piccio, L; Clerici, F; Albani, D; Mariani, C; Forloni, G; Bresolin, N; Goate, A; Scarpini, E
Candidate gene analysis of semaphorins in patients with Alzheimer's disease
2010 Villa, C; Venturelli, E; Fenoglio, C; De Riz, M; Scalabrini, D; Cortini, F; Serpente, M; Cantoni, C; Bresolin, N; Scarpini, E; Galimberti, D
GRN variability contributes to sporadic frontotemporal lobar degeneration
2010 Galimberti, D; Fenoglio, C; Cortini, F; Serpente, M; Venturelli, E; Villa, C; Clerici, F; Marcone, A; Benussi, L; Ghidoni, R; Gallone, S; Scalabrini, D; Restelli, I; Boneschi, F; Cappa, S; Binetti, G; Mariani, C; Rainero, I; Giordana, M; Bresolin, N; Scarpini, E
FUS/TLS genetic variability in sporadic frontotemporal lobar degeneration
2010 Cantoni, C; Fenoglio, C; Cortini, F; Venturelli, E; Villa, C; Clerici, F; Marcone, A; Benussi, L; Ghidoni, R; Gallone, S; Scalabrini, D; Franceschi, M; Cappa, S; Binetti, G; Mariani, C; Rainero, I; Giordana, M; Bresolin, N; Scarpini, E; Galimberti, D
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?
2010 Venturelli, E; Villa, C; Fenoglio, C; Clerici, F; Marcone, A; Benussi, L; Ghidoni, R; Gallone, S; Scalabrini, D; Cortini, F; Fumagalli, G; Cappa, S; Binetti, G; Franceschi, M; Rainero, I; Giordana, M; Mariani, C; Bresolin, N; Scarpini, E; Galimberti, D
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 Villa, C; Ghezzi, L; Pietroboni, A; Fenoglio, C; Cortini, F; Serpente, M; Cantoni, C; Ridolfi, E; Marcone, A; Benussi, L; Ghidoni, R; Jacini, F; Arighi, A; Fumagalli, G; Mandelli, A; Binetti, G; Cappa, S; Bresolin, N; Scarpini, E; Galimberti, D
Causal frontotemporal lobar degeneration mutations: a novel mutation in MAPT associated with non-fluent progressive aphasia phenotype
2011 Villa, C; Ghezzi, L; Pietroboni, A; Fenoglio, C; Cortini, F; Serpente, M; Cantoni, C; Ridolfi, E; Marcone, A; Benussi, L; Ghidoni, R; Jacini, F; Arighi, A; Fumagalli, G; Mandelli, A; Binetti, G; Cappa, S; Bresolin, N; Scarpini, E; Galimberti, D
Genetics and expression analysis of Sp4 transcription factor in patients with Alzheimer’s disease and frontotemporal lobar degeneration.
2011 Villa, C; Ghezzi, L; Fenoglio, C; Cortini, F; Serpente, M; Cantoni, C; Ridolfi, E; Marcone, A; Benussi, L; Ghidoni, R; Gallone, S; Cappa, S; Binetti, G; Rainero, I; Bresolin, N; Scarpini, E; Galimberti, D
From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder
2011 Cerami, C; Marcone, A; Galimberti, D; Villa, C; Scarpini, E; Cappa, S
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis
2011 Fenoglio, C; Cantoni, C; De Riz, M; Ridolfi, E; Cortini, F; Serpente, M; Villa, C; Comi, C; Monaco, F; Mellesi, L; Valzelli, S; Bresolin, N; Galimberti, D; Scarpini, E
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease
2011 Cortini, F; Fenoglio, C; Venturelli, E; Villa, C; Clerici, F; Serpente, M; Cantoni, C; Fumagalli, G; Mariani, C; Bresolin, N; Scarpini, E; Galimberti, D