FENOGLIO, CHIARA
FENOGLIO, CHIARA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
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 functional variant in ERAP1 predisposes to multiple sclerosis
2012 F.R. Guerini, R. Cagliani, D. Forni, C. Agliardi, D. Caputo, A. Cassinotti, D. Galimberti, C. Fenoglio, M. Biasin, R. Asselta, E. Scarpini, G.P. Comi, N. Bresolin, M.S. Clerici, M. Sironi
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
A Trans-Specific Polymorphism in ZC3HAV1 Is Maintained by Long-Standing Balancing Selection and May Confer Susceptibility to Multiple Sclerosis
2012 R. Cagliani, F.R. Guerini, M. Fumagalli, S. Riva, C. Agliardi, D. Galimberti, U. Pozzoli, A. Goris, B. Dubois, C. Fenoglio, D. Forni, S. Sanna, I. Zara, M. Pitzalis, M. Zoledziewska, F. Cucca, F. Marini, G.P. Comi, E. Scarpini, N. Bresolin, M. Clerici, M. Sironi
A91V variation of the perforin gene in patients with multiple sclerosis
2006 C. Comi, G. Cappellano, A. Ciocchetti, D. Galimberti, C. Fenoglio, E. Cerutti, L. Castelli, R. Mesturini, M. Carecchio, M. Leone, E. Scarpini, F. Monaco, U. Dianzani
Absence of mutations in TREM-2 coding region in early onset dementia
2007 C. Fenoglio, D. Galimberti, E. Venturelli, L. Piccio, D. Scalabrini, P. Panina, C. Buonsanti, C. Lovati, P.L. Baron, G. Forloni, C. Mariani, N. Bresolin, E. Scarpini
Absence of mutations in TREM-2 coding region in early onset dementia
2006 C. Fenoglio, D. Galimberti, E. Venturelli, L. Piccio, D. Scalabrini, P. Panina, C. Buonsanti, C. Lovati, P.L. Baron, G. Forloni, C. Mariani, N. Bresolin, E. Scarpini
Absence of mutations in TREM-2 coding region in patients with early onset dementia
2006 C. Fenoglio, D. Galimberti, E. Venturelli, L. Piccio, D. Scalabrini, P. Panina, C. Buonsanti, C. Lovati, P. Baron, G. Forloni, C. Mariani, N. Bresolin, E. Scarpini
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration
2007 C. Fenoglio, D. Galimberti, L. Piccio, D. Scalabrini, P. Panina, C. Buonsanti, E. Venturelli, C. Lovati, G. Forloni, C. Mariani, N. Bresolin, E. Scarpini
Age at symptom onset and death and disease duration in genetic frontotemporal dementia : an international retrospective cohort study
2020 K.M. Moore, J. Nicholas, M. Grossman, C.T. McMillan, D.J. Irwin, L. Massimo, V.M. Van Deerlin, J.D. Warren, N.C. Fox, M.N. Rossor, S. Mead, M. Bocchetta, B.F. Boeve, D.S. Knopman, N.R. Graff-Radford, L.K. Forsberg, R. Rademakers, Z.K. Wszolek, J.C. van Swieten, L.C. Jiskoot, L.H. Meeter, E.G. Dopper, J.M. Papma, J.S. Snowden, J. Saxon, M. Jones, S. Pickering-Brown, I. Le Ber, A. Camuzat, A. Brice, P. Caroppo, R. Ghidoni, M. Pievani, L. Benussi, G. Binetti, B.C. Dickerson, D. Lucente, S. Krivensky, C. Graff, L. Oijerstedt, M. Fallstrom, H. Thonberg, N. Ghoshal, J.C. Morris, B. Borroni, A. Benussi, A. Padovani, D. Galimberti, E. Scarpini, G.G. Fumagalli, I.R. Mackenzie, G.-.R. Hsiung, P. Sengdy, A.L. Boxer, H. Rosen, J.B. Taylor, M. Synofzik, C. Wilke, P. Sulzer, J.R. Hodges, G. Halliday, J. Kwok, R. Sanchez-Valle, A. Llado, S. Borrego-Ecija, I. Santana, M.R. Almeida, M. Tabuas-Pereira, F. Moreno, M. Barandiaran, B. Indakoetxea, J. Levin, A. Danek, J.B. Rowe, T.E. Cope, M. Otto, S. Anderl-Straub, A. de Mendonca, C. Maruta, M. Masellis, S.E. Black, P. Couratier, G. Lautrette, E.D. Huey, S. Sorbi, B. Nacmias, R. Laforce, M.-.L. Tremblay, R. Vandenberghe, P.V. Damme, E.J. Rogalski, S. Weintraub, A. Gerhard, C.U. Onyike, S. Ducharme, S.G. Papageorgiou, A.S.L. Ng, A. Brodtmann, E. Finger, R. Guerreiro, J. Bras, J.D. Rohrer, C. Heller, R.S. Convery, I.O. Woollacott, R.M. Shafei, J. Graff-Radford, D.T. Jones, C.M. Dheel, R. Savica, M.I. Lapid, M. Baker, J.A. Fields, R. Gavrilova, K. Domoto-Reilly, J.M. Poos, E.L. Van der Ende, J.L. Panman, L. Donker Kaat, H. Seelaar, A. Richardson, G. Frisoni, A. Mega, S. Fostinelli, H.-. Chiang, A. Alberici, A. Arighi, C. Fenoglio, H. Heuer, B. Miller, A. Karydas, J. Fong, M. Joao Leitao, B. Santiago, D. Duro, C. Ferreira, A. Gabilondo, M. De Arriba, M. Tainta, M. Zulaica, C. Ferreira, E. Semler, A. Ludolph, B. Landwehrmeyer, A.E. Volk, G. Miltenberger, A. Verdelho, S. Afonso, M.C. Tartaglia, M. Freedman, E. Rogaeva, C. Ferrari, I. Piaceri, V. Bessi, G. Lombardi, F. St-Onge, M.-. Dore, R. Bruffaerts, M. Vandenbulcke, J. Van den Stock, M.M. Mesulam, E. Bigio, C. Koros, J. Papatriantafyllou, C. Kroupis, L. Stefanis, C. Shoesmith, E. Robertson, G. Coppola, E.M. Da Silva Ramos, D. Geschwind
Alzheimer's disease: from pathogenesis to new perspectives for treatment
2008 D. Galimberti, C. Fenoglio, 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
Amyloid PET imaging and dementias: potential applications in detecting and quantifying early white matter damage
2022 A.M. Pietroboni, A. Colombi, T. Carandini, L. Sacchi, C. Fenoglio, G. Marotta, A. Arighi, M.A. De Riz, G.G. Fumagalli, M. Castellani, M. Bozzali, E. Scarpini, D. Galimberti
An emerging role for long non-coding RNA dysregulation in neurological disorders
2013 C. Fenoglio, E. Ridolfi, D. Galimberti, E. Scarpini
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