GHEZZI, LAURA
GHEZZI, LAURA
Dipartimento di Scienze Biomediche, Chirurgiche ed Odontoiatriche
A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation
2012 L. Ghezzi, E. Scarpini, M. Rango, A. Arighi, M.T. Bassi, E. Tenderini, M. De Riz, F. Jacini, G.G. Fumagalli, A.M. Pietroboni, D. Galimberti, N. Bresolin
A case of vanishing white matter disease due to the c.260C > T(p.Ala87Val) EIF2B3 mutation
2012 L. Ghezzi, M.T. Bassi, A.M. Pietroboni, G.G. Fumagalli, A. Arighi, M. Rango, M. De Riz, F. Jacini, D. Galimberti, 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
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 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 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
Alterations of host-gut microbiome interactions in multiple sclerosis
2022 C. Cantoni, Q. Lin, Y. Dorsett, L. Ghezzi, Z. Liu, Y. Pan, K. Chen, Y. Han, Z. Li, H. Xiao, M. Gormley, Y. Liu, S. Bokoliya, H. Panier, C. Suther, E. Evans, L. Deng, A. Locca, R. Mikesell, K. Obert, P. Newland, Y. Wu, A. Salter, A.H. Cross, P.I. Tarr, A. Lovett-Racke, L. Piccio, Y. Zhou
Alzheimer's disease: Clinical aspects and treatments
2014 L. Ghezzi
Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis : correlation with CSF β-amyloid levels and brain volumes
2019 A.M. Pietroboni, T. Carandini, A. Colombi, M. Mercurio, L. Ghezzi, G. Giulietti, M. Scarioni, A. Arighi, C. Fenoglio, M.A. De Riz, G.G. Fumagalli, P. Basilico, M. Serpente, M. Bozzali, E. Scarpini, D. Galimberti, G. Marotta
Balò’s concentric sclerosis : still to be considered as a variant of multiple sclerosis?
2015 A.M. Pietroboni, A. Arighi, M.A. De Riz, L. Ghezzi, A. Calvi, S. Avignone, E. Scola, D. Galimberti, F. Triulzi, E. Scarpini, L. Ghezzi
Behavioral and Neurophysiological Effects of Transcranial Direct Current Stimulation (tDCS) in Fronto-Temporal Dementia
2018 R. Ferrucci, S. Mrakic-Sposta, S. Gardini, F. Ruggiero, M. Vergari, F. Mameli, A. Arighi, M. Spallazzi, F. Barocco, G. Michelini, A.M. Pietroboni, L. Ghezzi, G.G. Fumagalli, G. D'Urso, P. Caffarra, E. Scarpini, A. Priori, S. Marceglia
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 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
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
Cerebrospinal Fluid Level of Aquaporin4: A New Window on Glymphatic System Involvement in Neurodegenerative Disease?
2019 A. Arighi, A. Di Cristofori, C. Fenoglio, S. Borsa, M. D'Anca, G.G. Fumagalli, M. Locatelli, G. Carrabba, A.M. Pietroboni, L. Ghezzi, T. Carandini, A. Colombi, M. Scarioni, M.A. De Riz, M. Serpente, P.M. Rampini, E. Scarpini, D. Galimberti
Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status
2016 L. Piccio, Y. Deming, J.L. Del Águila, L. Ghezzi, D.M. Holtzman, A.M. Fagan, C. Fenoglio, D. Galimberti, B. Borroni, C. Cruchaga
Circulating miRNAs as potential biomarkers in Alzheimer's disease
2014 D. Galimberti, C. Villa, C. Fenoglio, M. Serpente, L. Ghezzi, S.M.G. Cioffi, A. Arighi, G. Fumagalli, E. Scarpini
Cognitive predictors and correlations with biomarkers and functional imaging in patients with primary progressive aphasia
2012 P. Corti, E. Rotondo, R. Vimercati, F. Jacini, G. Fumagalli, A. Arighi, L. Ghezzi, N. Bresolin, D. Galimberti, E. Scarpini
CSF β-amyloid and white matter damage: A new perspective on Alzheimer's disease
2018 A.M. Pietroboni, M. Scarioni, T. Carandini, P. Basilico, M. Cadioli, G. Giulietti, A. Arighi, M. Caprioli, L. Serra, C. Sina, C. Fenoglio, L. Ghezzi, G.G. Fumagalli, M.A. De Riz, A. Calvi, F. Triulzi, M. Bozzali, E. Scarpini, D. Galimberti