FENOGLIO, CHIARA
FENOGLIO, CHIARA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
A functional variant in ERAP1 predisposes to multiple sclerosis
2012-01-01 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
A91V variation of the perforin gene in patients with multiple sclerosis
2006-01-01 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
2006-01-01 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
2007-07-03 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
2006-01-01 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
2007-01-01 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
2020-01-01 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
2008-01-01 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
2019-01-01 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?
2021-01-01 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
2020-01-01 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
ApoE e2 and e4 influence the susceptibility for Alzheimer’s disease but not other dementias
2007-01-01 D. Galimberti, C. Lovati, P. Bertora, E. Venturelli, G. Cislaghi, I. Guidi, C. Fenoglio, F. Cortini, F. Clerici, D. Finazzi, D. Albani, G. Forloni, N. Bresolin, C. Mariani, E. Scarpini
ApoE e2 decreases the susceptibility to develop Alzheimer's disease but not frontotemporal lobar degeneration, Lewy body disease or vascular dementia
2007-03-01 D. Galimberti, C. Lovati, E. Venturelli, P. Bertora, I. Guidi, C. Fenoglio, F. Cortini, G. Cislaghi, F. Clerici, G. Forloni, N. Bresolin, C. Mariani, E. Scarpini
Association between Alzheimer’s disease and the hypocretin receptor 2 gene
2011-01-01 I. Rainero, E. Rubino, D. Galimberti, S. Gallone, P. Fenoglio, C. Fenoglio, E. Scarpini, L. Pinessi
Association between VEGF gene and sporadic Alzheimer's disease.
2005-01-01 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli-Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer’s Disease
2005-01-01 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Association of neuronal nitric oxide synthase C276T polymorphism with Azheimer's disease
2005-01-01 A. Gatti, D. Galimberti, C. Lovati, C. Fenoglio, E. Venturelli, C. Mariani, G. Forloni, N. Bresolin, E. Scarpini
Association study to evaluate the serotonin trasporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy
2008-12-01 D. Albani, F. Prato, C. Fenoglio, S. Batelli, S. Dusi, S. De Mauro, L. Polito, C. Lovati, D. Galimberti, C. Mariani, E. Scarpini, G. Forloni
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion : late-onset psychotic clinical presentation
2013-09-01 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
2011-01-01 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