VILLA, CHIARA
VILLA, CHIARA
Universita' degli Studi di MILANO
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 D. Galimberti, C. Villa, L. Ghezzi, A. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E. Scarpini
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E.A. Scarpini, D. Galimberti
Anthropological and paleopathological study of middle age human skeletal remains from Fara Gera d'Adda (Bergamo, Northern Italy)
2008 C. Villa, A. Mazzucchi, C. Cattaneo
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion : late-onset psychotic clinical presentation
2013 D. Galimberti, C. Fenoglio, M. Serpente, C. Villa, R. Bonsi, A. Arighi, G.G. Fumagalli, R. Del Bo, A.C. Bruni, M. Anfossi, A. Clodomiro, C. Cupidi, B. Nacmias, S. Sorbi, I. Piaceri, S. Bagnoli, V. Bessi, A. Marcone, C. Cerami, S.F. Cappa, M. Filippi, F. Agosta, G. Magnani, G. Comi, M. Franceschi, I. Rainero, M.T. Giordana, E. Rubino, P. Ferrero, E. Rogaeva, Z. Xi, A. Confaloni, P. Piscopo, G. Bruno, G. Talarico, A. Cagnin, F. Clerici, B. Dell'Osso, G.P. Comi, A.C. Altamura, C. Mariani, 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
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis
2007 D. Scalabrini, C. Fenoglio, E. Scarpini, M. De Riz, C. Comi, E. Venturelli, F. Cortini, M. Piola, C. Villa, P. Naldi, F. Monaco, N. Bresolin, D. Galimberti
Causal frontotemporal de generation mutations : a novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E.A. Scarpini, D. Galimberti
Causal frontotemporal lobar degeneration mutations : a novel mutation in MAPT associated with non-fluent Progressive Aphasia phenotype
2011 C. Villa, L. Ghezzi, A.M. Pietroboni, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Ridolfi, A. Marcone, L. Benussi, R. Ghidoni, F. Jacini, A. Arighi, G.G. Fumagalli, A. Mandelli, G. Binetti, S. Cappa, N. Bresolin, E.A. Scarpini, D. Galimberti
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
CHMP5 and BAG1 are protective factors against sporadic Frontotemporal Lobar Degeneration
2010 D. Galimberti, C. Villa, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, S. Cappa, G. Binetti, I. Rainero, N. Bresolin, C. Mariani, 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
Common and unusual urogenital Crohn's disease complications : spectrum of cross-sectional imaging findings
2013 M. Tonolini, C. Villa, A. Campari, A. Ravelli, R. Bianco, G. Cornalba
DCUN1D1 is a risk factor for frontotemporal lobar degeneration
2009 C. Villa, E. Venturelli, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, S. Gallone, D. Scalabrini, F. Cortini, M. Serpente, F. Martinelli Boneschi, S. Cappa, G. Binetti, C. Mariani, I. Rainero, M.T. Giordana, 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
Forensic age estimation based on the trabecular bone changes of the pelvic bone using post-mortem CT
2013 C. Villa, M.N. Hansen, J. Buckberry, C. Cattaneo, N. Lynnerup
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease
2008 C. Fenoglio, D. Galimberti, F. Cortini, J.S.K. Kauwe, E. Venturelli, I. Guidi, D. Scalabrini, C. Villa, K. Mayo, E. DALLA VALLE, C. Lovati, C. Mariani, N. Bresolin, A.M. Goate, E. Scarpini
Genetic and functional analysis of progranulin gene variants in Alzheimer's disease.
2008 C. Fenoglio, D. Galimberti, F. Cortini, J.S.K. Kauwe, E. Venturelli, D. Scalabrini, C. Lovati, C. Villa, I. Restelli, D. Albani, C. Mariani, G. Forloni, N. Bresolin, A.M. Goate, E. Scarpini
Genetic and functional analysis of progranulin gene variants in patients with Alzheimer's disease
2008 C. Fenoglio, F. Cortini, E. Venturelli, I. Guidi, D. Galimberti, C. Villa, J.S.K. Kauwe, K. Mayo, E. Dalla Valle, C. Lovati, C. Mariani, E. Scarpini, N. Bresolin, A.M. Goate, D. Scalabrini
Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration
2012 C. Villa, L. Ghezzi, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, M. Serpente, C. Cantoni, E. Ridolfi, R. Bonsi, C. Cerami, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, C. Mariani, N. Bresolin, E. Scarpini, D. Galimberti
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