VILLA, CHIARA
VILLA, CHIARA
Universita' degli Studi di MILANO
Transperineal perineal ultrasound versus magnetic resonance imaging in the assessment of perianal Crohn's disease
2013 G. Maconi, M. Tonolini, M. Monteleone, C. Bezzio, F. Furfaro, C. Villa, A. Campari, A. Dellʼera, G. Sampietro, S. Ardizzone, R. de Franchis
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
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
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
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
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia
2012 D. Galimberti, B. Dell'Osso, C. Fenoglio, C. Villa, F. Cortini, M. Serpente, S. Kittel Schneider, J. Weigl, M. Neuner, J. Volkert, C. Leonhard, D.G. Olmes, J. Kopf, C. Cantoni, E. Ridolfi, C. Palazzo, L. Ghezzi, N. Bresolin, A.C. Altamura, E. Scarpini, A. Reif
Role of hnRNP-A1 and miR-590-3p in neuronal death : genetics and expression analysis in patients with Alzheimer’s disease and frontotemporal lobar degeneration
2011 E. Ridolfi, C. Villa, C. Fenoglio, M.A. De Riz, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, M. Serpente, C. Cantoni, G. Fumagalli, F. Martinelli Boneschi, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini, 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
OLR1 and its regulatory miR-369-3p : genetics and expression analysis
2011 M. Serpente, C. Fenoglio, F. Clerici, R. Ghidoni, L. Benussi, S. Gallone, A. Marcone, C. Villa, F. Cortini, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
Role of OLR1 and its regulating has-miR369-3p in Alzheimer’s disease: genetic and expression analysis
2011 D. Galimberti, M. Serpente, C. Fenoglio, C. Villa, F. Cortini, C. Cantoni, E. Ridolfi, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini
Oligodendrocyte Lineage Transcription Factor 2 role in Alzheimer’s disease : association and expression analysis
2011 F. Cortini, C. Fenoglio, F. Clerici, L. Benussi, R. Ghidoni, S. Gallone, A. Marcone, C. Villa, M. Serpente, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
Oligodendrocyte lineage transcription factor-2 role in Alzheimer’s disease : association and expression analysis
2011 F. Cortini, C. Fenoglio, F. Clerici, L. Benussi, R. Ghidoni, S. Gallone, A. Marcone, C. Villa, M. Serpente, C. Cantoni, E. Ridolfi, M. Franceschi, G. Binetti, I. Rainero, S. Cappa, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
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
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
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetic and expression analysis
2011 D. Galimberti, M. Serpente, C. Fenoglio, C. Villa, F. Cortini, C. Cantoni, E. Ridolfi, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer’s disease : genetics and expression analysis
2011 M. Serpente, C. Fenoglio, C. Villa, F. Cortini, C. Cantoni, E. Ridolfi, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, F..M. Boneschi, S. Gallone, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E. Scarpini, D. Galimberti
Role of hnRNP-A1 and miR-590-3p in Neuronal Death : Genetics and Expression Analysis in Patients with Alzheimer Disease and Frontotemporal Lobar Degeneration
2011 C. Villa, C. Fenoglio, M.A. De Riz, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, M. Serpente, C. Cantoni, G. Fumagalli, F.M. Boneschi, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
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
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