SERPENTE, MARIA
SERPENTE, MARIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
A case of bipolar disorder developing into atypical parkinsonism and presenting with frontotemporal asymmetrical brain degeneration : A TREDEM Registry Case Report
2020 M.E. Di Battista, C. Dell'Acqua, D. Galimberti, M. Serpente, F. Boccaletto, M. Gallucci
A Case with Early Onset Alzheimer's Disease, Frontotemporal Hypometabolism, ApoE Genotype ϵ 4/ ϵ 4 and C9ORF72 Intermediate Expansion : A Treviso Dementia (TREDEM) Registry Case Report
2019 M. Gallucci, C. Dell'Acqua, C. Bergamelli, C. Fenoglio, M. Serpente, D. Galimberti, V. Fiore, S. Medea, M. Gregianin, M.E. Di Battista
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
2015 R. Ferrari, M. Grassi, E. Salvi, B. Borroni, F. Palluzzi, D. Pepe, F. D'Avila, A. Padovani, S. Archetti, I. Rainero, E. Rubino, L. Pinessi, L. Benussi, G. Binetti, R. Ghidoni, D. Galimberti, E. Scarpini, M. Serpente, G. Rossi, G. Giaccone, F. Tagliavini, B. Nacmias, I. Piaceri, S. Bagnoli, A.C. Bruni, R.G. Maletta, L. Bernardi, A. Postiglione, G. Milan, M. Franceschi, A.A. Puca, V. Novelli, C. Barlassina, N. Glorioso, P. Manunta, A. Singleton, D. Cusi, J. Hardy, P. Momeni
A Novel Automated Chemiluminescence Method for Detecting Cerebrospinal Fluid Amyloid-Beta 1-42 and 1-40, Total Tau and Phosphorylated-Tau: Implications for Improving Diagnostic Performance in Alzheimer’s Disease
2022 M. Arcaro, C. Fenoglio, M. Serpente, A. Arighi, G.G. Fumagalli, L. Sacchi, S. Floro, M. D’Anca, F. Sorrentino, C. Visconte, A. Perego, 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
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
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
Analysis of C9orf72 Intermediate Alleles in a Retrospective Cohort of Neurological Patients: Risk Factors for Alzheimer's Disease?
2021 M. Serpente, C. Fenoglio, A. Arighi, G.G. Fumagalli, M. Arcaro, F. Sorrentino, C. Visconte, E. Scarpini, D. Galimberti
Anti-Cholinergic Derangement of Cortical Metabolism on 18F-FDG PET in a Patient with Frontotemporal Lobar Degeneration Dementia : a Case of the TREDEM Registry
2020 M. Gallucci, C. Pallucca, M.E. DI Battista, C. Bergamelli, V. Fiore, F. Boccaletto, M. Fiorini, D. Perra, G. Zanusso, C. Fenoglio, M. Serpente, D. Galimberti, L. Bonanni
Aquaporin-4 cerebrospinal fluid levels are higher in neurodegenerative dementia: looking at glymphatic system dysregulation
2022 A. Arighi, M. Arcaro, G.G. Fumagalli, T. Carandini, A.M. Pietroboni, L. Sacchi, C. Fenoglio, M. Serpente, F. Sorrentino, G. Isgrò, F. Turkheimer, E. Scarpini, D. Galimberti
Association between enlarged perivascular spaces and cerebrospinal fluid aquaporin-4 and tau levels: report from a memory clinic
2023 L. Sacchi, M. Arcaro, T. Carandini, A.M. Pietroboni, G.G. Fumagalli, C. Fenoglio, M. Serpente, F. Sorrentino, C. Visconte, M. Pintus, G. Conte, V.E. Contarino, E. Scarpini, F. Triulzi, D. Galimberti, A. Arighi
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
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
2011 E. Venturelli, C. Villa, C. Fenoglio, F. Clerici, A. Marcone, L. Benussi, R. Ghidoni, S. Gallone, F. Cortini, M. Serpente, C. Cantoni, G. Fumagalli, E. Ridolfi, S. Cappa, G. Binetti, M. Franceschi, I. Rainero, M.T. Giordana, C. Mariani, N. Bresolin, E.A. Scarpini, D. Galimberti
C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder
2014 D. Galimberti, A. Reif, B. Dell'Osso, C. Palazzo, C. Villa, C. Fenoglio, S. Kittel Schneider, C. Leonhard, D. Olmes, M. Serpente, R. Paoli, A. Altamura, E. Scarpini
C9ORF72 hexanucleotide repeat expansion frequency in patients with Paget's disease of bone
2020 E. Rubino, M. Di Stefano, D. Galimberti, M. Serpente, E. Scarpini, C. Fenoglio, M. Bo, I. Rainero
C9ORF72 repeat expansion not detected in patients with multiple sclerosis
2014 C. Fenoglio, M. De Riz, C. Villa, M. Serpente, E. Ridolfi, R. Bonsi, S.M.G. Cioffi, C. Barone, A. Pietroboni, A. Calvi, E. Scarpini, D. Galimberti
C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts
2020 B. Costa, C. Manzoni, M. Bernal-Quiros, D.A. Kia, M. Aguilar, I. Alvarez, V. Alvarez, O. Andreassen, M. Anfossi, S. Bagnoli, L. Benussi, L. Bernardi, G. Binetti, D. Blackburn, M. Boada, B. Borroni, L. Bowns, G. Bråthen, A.C. Bruni, H. Chiang, J. Clarimon, S. Colville, M.E. Conidi, T.E. Cope, C. Cruchaga, C. Cupidi, M.E. Di Battista, J. Diehl-Schmid, M. Diez-Fairen, O. Dols-Icardo, E. Durante, D. Flisar, F. Frangipane, D. Galimberti, M. Gallo, M. Gallucci, R. Ghidoni, C. Graff, J.H. Grafman, M. Grossman, J. Hardy, I. Hernández, G.J. Holloway, E.D. Huey, I. Illán-Gala, A. Karydas, B. Khoshnood, M.G. Kramberger, M. Kristiansen, P.A. Lewis, A. Lleó, G.K. Madhan, R. Maletta, A. Maver, M. Menendez-Gonzalez, G. Milan, B. Miller, M.O. Mol, P. Momeni, S. Moreno-Grau, C.M. Morris, B. Nacmias, C. Nilsson, V. Novelli, L. Öijerstedt, A. Padovani, S. Pal, Y. Panchbhaya, P. Pastor, B. Peterlin, I. Piaceri, S. Pickering-Brown, Y.A. Pijnenburg, A.A. Puca, I. Rainero, A. Rendina, A.M. Richardson, E. Rogaeva, B. Rogelj, S. Rollinson, G. Rossi, C. Rossmeier, J.B. Rowe, E. Rubino, A. Ruiz, R. Sanchez-Valle, S.B. Sando, A.F. Santillo, J. Saxon, E. Scarpini, M. Serpente, N. Smirne, S. Sorbi, E. Suh, F. Tagliavini, J.C. Thompson, J.Q. Trojanowski, V.M. Van Deerlin, J. Van der Zee, C. Van Broeckhoven, J. van Rooij, J.C. Van Swieten, A. Veronesi, E. Vitale, M.L. Waldö, C. Woodward, J. Yokoyama, V. Escott-Price, J.M. Polke, R. Ferrari
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