Sfoglia per Autore
Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations
2013 N. Ticozzi, C. Tiloca, N.E. Mencacci, C. Morelli, A. Doretti, D. Rusconi, C. Colombrita, D. Sangalli, F. Verde, P. Finelli, S. Messina, A. Ratti, V. Silani
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis
2013 D. Calini, L. Corrado, R. Del Bo, S. Gagliardi, V. Pensato, F. Verde, S. Corti, L. Mazzini, P. Milani, B. Castellotti, C. Bertolin, G. Sorarù, C. Cereda, G.P. Comi, S. D'Alfonso, C. Gellera, N. Ticozzi, J.E. Landers, A. Ratti, V. Silani
An old woman with pressure ulcer, rigidity, and opisthotonus: never forget tetanus!
2014 F. Verde, G. Riboldi, C. Zappa, M. Ferretti, V. Silani, D. Mari, A. Priori
Amyotrophic lateral sclerosis: Epidemiology and risk factors
2016 F. Verde, N. Ticozzi
MRI abnormalities found 1 year prior to symptom onset in a case of Creutzfeldt–Jakob disease
2016 F. Verde, N. Ticozzi, S. Messina, N. Calcagno, F. Girotti, L. Maderna, F. Moda, E. Scola, A. Falini, F. Tagliavini, V. Silani
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
2016 K.P. Kenna, P.T.C. van Doormaal, A.M. Dekker, N. Ticozzi, B.J. Kenna, F.P. Diekstra, W. van Rheenen, K.R. van Eijk, A.R. Jones, P. Keagle, A. Shatunov, W. Sproviero, B.N. Smith, M.A. van Es, S.D. Topp, A. Kenna, J.W. Miller, C. Fallini, C. Tiloca, R.L. Mclaughlin, C. Vance, C. Troakes, C. Colombrita, G. Mora, A. Calvo, F. Verde, S. Al Sarraj, A. King, D. Calini, J. de Belleroche, F. Baas, A.J. van der Kooi, M. de Visser, A.L.M.A. Ten Asbroek, P.C. Sapp, D. McKenna Yasek, M. Polak, S. Asress, J.L. Muñoz Blanco, T.M. Strom, T. Meitinger, K.E. Morrison, G. LAURIA PINTER, K.L. Williams, P.N. Leigh, G.A. Nicholson, I.P. Blair, C.S. Leblond, P.A. Dion, G.A. Rouleau, H. Pall, P.J. Shaw, M.R. Turner, K. Talbot, F. Taroni, K.B. Boylan, M. Van Blitterswijk, R. Rademakers, J. Esteban Pérez, A. García Redondo, P. Van Damme, W. Robberecht, A. Chio, C. Gellera, C. Drepper, M. Sendtner, A. Ratti, J.D. Glass, J.S. Mora, N.A. Basak, O. Hardiman, A.C. Ludolph, P.M. Andersen, J.H. Weishaupt, R.H. Brown, A. Al Chalabi, V. Silani, C.E. Shaw, L.H. van den Berg, J.H. Veldink, J.E. Landers
The validation of the Italian Edinburgh cognitive and behavioural ALS screen (ECAS)
2016 B. Poletti, F. Solca, L. Carelli, F. Madotto, A. Lafronza, A. Faini, A. Monti, S. Zago, D. Calini, C. Tiloca, A. Doretti, F. Verde, A. Ratti, N. Ticozzi, S. Abrahams, V. Silani
A novel nonsense ATP7A pathogenic variant in a family exhibiting a variable occipital horn syndrome phenotype
2017 M..T. Bonati, F. Verde, U. Hladnik, P. Cattelan, L. Campana, C. Castronovo, N. Ticozzi, L. Maderna, C. Colombrita, S. Papa, P. Banfi, V. Silani
Mutations in the vesicular trafficking protein Annexin A11 are associated with amyotrophic lateral sclerosis
2017 B.N. Smith, S.D. Topp, C. Fallini, H. Shibata, H. Chen, C. Troakes, A. King, N. Ticozzi, K.P. Kenna, A. Soragia Gkazi, J.W. Miller, A. Sato, D.M. Dias, M. Jeon, C. Vance, C.H. Wong, M. De Majo, W. Kattuah, J.C. Mitchell, E.L. Scotter, N.W. Parkin, P.C. Sapp, M. Nolan, P.J. Nestor, M. Simpson, M. Weale, M. Lek, F. Baas, J.M.V. De Jong, A.L.M.A. Ten Asbroek, A.G. Redondo, J. Esteban Pérez, C. Tiloca, F. Verde, S. Duga, N. Leigh, H. Pall, K.E. Morrison, A. Al Chalabi, P.J. Shaw, J. Kirby, M.R. Turner, K. Talbot, O. Hardiman, J.D. Glass, J. De Belleroche, M. Maki, S.E. Moss, C. Miller, C. Gellera, A. Ratti, S. Al Sarraj, R.H. Brown, V. Silani, J.E. Landers, C.E. Shaw
The role of de novo mutations in the development of amyotrophic lateral sclerosis
2017 P.T. van Doormaal, N. Ticozzi, J.H. Weishaupt, K. Kenna, F.P. Diekstra, F. Verde, P.M. Andersen, A.M. Dekker, C. Tiloca, N. Marroquin, D.J. Overste, V. Pensato, P. Nürnberg, S.L. Pulit, R.D. Schellevis, D. Calini, J. Altmüller, L.C. Francioli, B. Muller, B. Castellotti, S. Motameny, A. Ratti, J. Wolf, C. Gellera, A.C. Ludolph, L.H. van den Berg, C. Kubisch, J.E. Landers, J.H. Veldink, V. Silani, A.E. Volk
The multisystem degeneration amyotrophic lateral sclerosis - neuropathological staging and clinical translation
2017 F. Verde, K. Del Tredici, H. Braak, A.C. Ludolph
Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression
2018 P. Steinacker, F. Verde, L. Fang, E. Feneberg, P. Oeckl, S. Roeber, S. Anderl-Straub, A. Danek, J. Diehl-Schmid, K. Fassbender, K. Fliessbach, H. Foerstl, A. Giese, H. Jahn, J. Kassubek, J. Kornhuber, G.B. Landwehrmeyer, M. Lauer, E.H. Pinkhardt, J. Prudlo, A. Rosenbohm, A. Schneider, M.L. Schroeter, H. Tumani, C.A.F. Von Arnim, J. Weishaupt, P. Weydt, A.C. Ludolph, D. Yilmazer Hanke, M. Otto
Chromogranin A levels in the cerebrospinal fluid of patients with amyotrophic lateral sclerosis
2018 F. Verde, P. Steinacker, P. Oeckl, J.H. Weishaupt, A. Rosenbohm, V. Silani, A.C. Ludolph, M. Otto
Multicenter evaluation of neurofilaments in early symptom onset amyotrophic lateral sclerosis
2018 E. Feneberg, P. Oeckl, P. Steinacker, F. Verde, C. Barro, P. Van Damme, E. Gray, J. Grosskreutz, C. Jardel, J. Kuhle, S. Koerner, F. Lamari, M. Del Mar Amador, B. Mayer, C. Morelli, P. Muckova, S. Petri, K. Poesen, J. Raaphorst, F. Salachas, V. Silani, B. Stubendorff, M.R. Turner, M.M. Verbeek, J.H. Weishaupt, P. Weydt, A.C. Ludolph, M. Otto
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
2018 A. Nicolas, K.P. Kenna, A.E. Renton, N. Ticozzi, F. Faghri, R. Chia, J.A. Dominov, B.J. Kenna, M.A. Nalls, P. Keagle, A.M. Rivera, W. van Rheenen, N.A. Murphy, J.J.F.A. van Vugt, J.T. Geiger, R.A. Van der Spek, H.A. Pliner, N. Shankaracharya, B.N. Smith, G. Marangi, S.D. Topp, Y. Abramzon, A.S. Gkazi, J.D. Eicher, A. Kenna, G. Mora, A. Calvo, L. Mazzini, N. Riva, J. Mandrioli, C. Caponnetto, S. Battistini, P. Volanti, V. La Bella, F.L. Conforti, G. Borghero, S. Messina, I.L. Simone, F. Trojsi, F. Salvi, F.O. Logullo, S. D'Alfonso, L. Corrado, M. Capasso, L. Ferrucci, C.D.A.M. Moreno, S. Kamalakaran, D.B. Goldstein, A.D. Gitler, T. Harris, R.M. Myers, H. Phatnani, R.L. Musunuri, U.S. Evani, A. Abhyankar, M.C. Zody, J. Kaye, S. Finkbeiner, S.K. Wyman, A. Lenail, L. Lima, E. Fraenkel, C.N. Svendsen, L.M. Thompson, J.E. Van Eyk, J.D. Berry, T.M. Miller, S.J. Kolb, M. Cudkowicz, E. Baxi, M. Benatar, J.P. Taylor, E. Rampersaud, G. Wu, J. Wuu, G. Lauria, F. Verde, I. Fogh, C. Tiloca, G.P. Comi, G. Sorarù, C. Cereda, P. Corcia, H. Laaksovirta, L. Myllykangas, L. Jansson, M. Valori, J. Ealing, H. Hamdalla, S. Rollinson, S. Pickering-Brown, R.W. Orrell, K.C. Sidle, A. Malaspina, J. Hardy, A.B. Singleton, J.O. Johnson, S. Arepalli, P.C. Sapp, D. McKenna-Yasek, M. Polak, S. Asress, S. Al-Sarraj, A. King, C. Troakes, C. Vance, J. de Belleroche, F. Baas, A.L.M.A. Ten Asbroek, J.L. Muñoz-Blanco, D.G. Hernandez, J. Ding, J.R. Gibbs, S.W. Scholz, M.K. Floeter, R.H. Campbell, F. Landi, R. Bowser, S.M. Pulst, J.M. Ravits, D.J.L. Macgowan, J. Kirby, E.P. Pioro, R. Pamphlett, J. Broach, G. Gerhard, T.L. Dunckley, C.B. Brady, N.W. Kowall, J.C. Troncoso, I. Le Ber, K. Mouzat, S. Lumbroso, T.D. Heiman-Patterson, F. Kamel, L. Van Den Bosch, R.H. Baloh, T.M. Strom, T. Meitinger, A. Shatunov, K.R. Van Eijk, M. de Carvalho, M. Kooyman, B. Middelkoop, M. Moisse, R.L. Mclaughlin, M.A. Van Es, M. Weber, K.B. Boylan, M. Van Blitterswijk, R. Rademakers, K.E. Morrison, A.N. Basak, J.S. Mora, V.E. Drory, P.J. Shaw, M.R. Turner, K. Talbot, O. Hardiman, K.L. Williams, J.A. Fifita, G.A. Nicholson, I.P. Blair, G.A. Rouleau, J. Esteban-Pérez, A. García-Redondo, A. Al-Chalabi, E. Rogaeva, L. Zinman, L.W. Ostrow, N.J. Maragakis, J.D. Rothstein, Z. Simmons, J. Cooper-Knock, A. Brice, S.A. Goutman, E.L. Feldman, S.B. Gibson, F. Taroni, A. Ratti, C. Gellera, P. Van Damme, W. Robberecht, P. Fratta, M. Sabatelli, C. Lunetta, A.C. Ludolph, P.M. Andersen, J.H. Weishaupt, W. Camu, J.Q. Trojanowski, V.M. Van Deerlin, R.H. Brown, L.H. van den Berg, J.H. Veldink, M.B. Harms, J.D. Glass, D.J. Stone, P. Tienari, V. Silani, A. Chiò, C.E. Shaw, B.J. Traynor, J.E. Landers
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
2018 M. de Majo, S.D. Topp, B.N. Smith, A.L. Nishimura, H. Chen, A.S. Gkazi, J. Miller, C.H. Wong, C. Vance, F. Baas, A.L.M.A. ten Asbroek, K.P. Kenna, N. Ticozzi, A.G. Redondo, J. Esteban-Pérez, C. Tiloca, F. Verde, S. Duga, K.E. Morrison, P.J. Shaw, J. Kirby, M.R. Turner, K. Talbot, O. Hardiman, J.D. Glass, J. de Belleroche, C. Gellera, A. Ratti, A. Al-Chalabi, R.H. Brown, V. Silani, J.E. Landers, C.E. Shaw
Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis
2019 F. Verde, P. Steinacker, J.H. Weishaupt, J. Kassubek, P. Oeckl, S. Halbgebauer, H. Tumani, C.A.F. Von Arnim, J. Dorst, E. Feneberg, B. Mayer, H. Müller, M. Gorges, A. Rosenbohm, A.E. Volk, V. Silani, A.C. Ludolph, M. Otto
PON1 is a disease modifier gene in amyotrophic lateral sclerosis : association of the Q192R polymorphism with bulbar onset and reduced survival
2019 F. Verde, C. Tiloca, C. Morelli, A. Doretti, B. Poletti, L. Maderna, S. Messina, D. Gentilini, I. Fogh, A. Ratti, V. Silani, N. Ticozzi
Neurochemical biomarkers in amyotrophic lateral sclerosis
2019 F. Verde, V. Silani, M. Otto
Cerebrospinal fluid phosphorylated neurofilament heavy chain and chitotriosidase in primary lateral sclerosis
2020 F. Verde, G. Zaina, C. Bodio, M.O. Borghi, D. Soranna, S. Peverelli, N. Ticozzi, C. Morelli, A. Doretti, S. Messina, L. Maderna, C. Colombrita, V. Gumina, C. Tiloca, P.L. Meroni, A. Zambon, A. Ratti, V. Silani
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