Sfoglia per Autore
GRN Asp22fs mutation is associated with highly variable age at onset, clinical phenotype and brain atrophy
2010 A. Pietroboni, G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Rotondo, P. Corti, N. Bresolin, D. Galimberti, E. Scarpini
GRN Asp22fs mutation is associated with heterogeneous neurodegenerative clinical phenotypes
2010 D. Galimberti, A. Pietroboni, G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, C. Cantoni, M. Serpente, M.T. Bassi, 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
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
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
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.
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
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
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, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, M. Serpente, C. Cantoni, G.G. Fumagalli, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M. Giordana, 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
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
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred
2011 A.M. Pietroboni, G.G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Rotondo, S.P. Corti, M. Carecchio, M. Bassi, N. Bresolin, D. Galbiati, D. Galimberti, E. Scarpini
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
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. Scarpini, D. Galimberti
Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease
2011 F. Cortini, C. Fenoglio, E. Venturelli, C. Villa, F. Clerici, M. Serpente, C. Cantoni, G. Fumagalli, C. Mariani, 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
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
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
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
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