Sfoglia per Autore
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
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
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
Causal frontotemporal degeneration mutations : a novel MAPT mutation associated with clinical phenotype of progressive nonfluent aphasia
2011 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, D. Galimberti
Phenotypic heterogeneity of the progranulin gene Asp22fs mutation in a large Italian kindred
2011 G. Fumagalli, A.M. Pietroboni, 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.A. Scarpini
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred
2011 A.M. Pietroboni, G. Fumagalli, L. Ghezzi, C. Fenoglio, F. Cortini, M. Serpente, C. Cantoni, E. Rotondo, P. Corti, N. Bresolin, D. Galimberti, 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
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
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
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
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
The impact of osteopontin gene variations on multiple sclerosis development and progression
2012 C. Comi, G. Cappellano, A. Chiocchetti, E. Orilieri, S. Buttini, L. Ghezzi, D. Galimberti, F. Guerini, N. Barizzone, F. Perla, M. Leone, S. D'Alfonso, D. Caputo, E. Scarpini, R. Cantello, U. Dianzani
Two cases of early onset FTLD due to chromosome 9 hexanucleotide repeats
2012 A. Arighi, D. Galimberti, F. Jacini, G. Fumgalli, L. Ghezzi, A. Pietroboni, M. DE RIZ, C. Fenoglio, M. Serpente, E. Ridolfi, N. Bresolin, E. Scarpini
Frequency of autosomal dominant mutations in an Italian population of patients with frontotemporal lobar degeneration
2012 G.G. Fumagalli, A. Arighi, D. Galimberti, F. Jacini, L. Ghezzi, A.M. Pietroboni, M. De Riz, C. Fenoglio, M. Serpente, E. Ridolfi, N. Bresolin, 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
Genetics and expression analysis of the transcription factor Sp4 in patients with Alzheimer’s disease and frontotemporal lobar degeneration
2012 C. Villa, C. Fenoglio, M. Serpente, F. Clerici, L. Benussi, R. Ghidoni, A. Marcone, S. Cappa, M. Franceschi, I. Rainero, S. Gallone, E. Ridolfi, L. Ghezzi, R. Bonsi, C. Cerami, G. Binetti, N. Bresolin, C. Mariani, E. Scarpini, D. Galimberti
Genetics and expression analysis of the transcription factor Sp4 in patients with Alzheimer’s disease and frontotemporal lobar degeneration
2012 D. Galimberti, C. Villa, C. Fenoglio, M. Serpente, R. Ghidoni, L. Benussi, A. Marcone, S. Cappa, F. Clerici, M. Franceschi, I. Rainero, S. Gallone, E. Ridolfi, L. Ghezzi, R. Bonsi, C. Cerami, G. Binetti, C. Mariani, N. Bresolin, E. Scarpini
A case of vanishing white-matter disease due to the c.260C>T (p.Ala87Val) EIF2B3 mutation
2012 L. Ghezzi, M. Bassi, A. Pietroboni, G. Fumagalli, A. Arighi, M. Rango, M. De Riz, F. Jacini, D. Galimberti, N. Bresolin, E. Scarpini
Validation of the Italian Addenbrooke’s cognitive examination revised (ACE-R) as a screening test
2012 M. Mercurio, E. Rotondo, P. Corti, R. Vimercati, F. Jacini, G. Fumagalli, A. Arighi, L. Ghezzi, N. Bresolin, D. Galimberti, E. Scarpini
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