TICOZZI, NICOLA
TICOZZI, NICOLA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
2014 I. Fogh, A. Ratti, C. Gellera, K. Lin, C. Tiloca, V. Moskvina, L. Corrado, G. Sorarù, C. Cereda, S. Corti, D. Gentilini, D. Calini, B. Castellotti, L. Mazzini, G. Querin, S. Gagliardi, R. Del Bo, F.L. Conforti, G. Siciliano, M. Inghilleri, F. Saccà, P. Bongioanni, S. Penco, M. Corbo, S. Sorbi, M. Filosto, A. Ferlini, A.M. Di Blasio, S. Signorini, A. Shatunov, A. Jones, P.J. Shaw, K.E. Morrison, A.E. Farmer, P. Van Damme, W. Robberecht, A. Chiò, B.J. Traynor, M. Sendtner, J. Melki, V. Meininger, O. Hardiman, P.M. Andersen, N.P. Leigh, J.D. Glass, D. Overste, F.P. Diekstra, J.H. Veldink, M.A. van Es, C.E. Shaw, M.E. Weale, C.M. Lewis, J. Williams, R.H. Brown, J.E. Landers, N. Ticozzi, M. Ceroni, E. Pegoraro, G.P. Comi, S. D'Alfonso, L.H. Van Den Berg, F. Taroni, A. Al Chalabi, J. Powell, 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
A preliminary comparison between ECAS and ALS-CBS in classifying cognitive–behavioural phenotypes in a cohort of non-demented amyotrophic lateral sclerosis patients
2021 L.C. Greco, A. Lizio, J. Casiraghi, V.A. Sansone, L. Tremolizzo, N. Riva, F. Solca, S. Torre, N. Ticozzi, M. Filippi, V. Silani, B. Poletti, C. Lunetta
A review of options for treating sialorrhea in amyotrophic lateral sclerosis
2015 P. Banfi, N. Ticozzi, A. Lax, G.A. Guidugli, A. Nicolini, V. Silani
Advance care planning and mental capacity in ALS: a current challenge for an unsolved matter
2020 B. Poletti, L. Carelli, C. Lunetta, N. Ticozzi, V. Silani
ALS genes: a mutational screening in a large cohort of Italian patients
2008 C. Gellera, N. Ticozzi, B. Castelletti, C. Colombrita, M. Plumari, C. Bragato, L. Moranti, D. Testa, A. Bellino, A. Ratti, V. Silani
ALS Genes: mutational analysis in a large cohort of Italian patients
2009 C. Gellera, N. Ticozzi, A. Ratti, L. Corrado, B. Castellotti, C. Colombrita, M. Plumari, Y. Carlomagno, C. Bragato, L. Mazzini, F. Taroni, V. Silani
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
Amyotrophic lateral sclerosis: Epidemiology and risk factors
2016 F. Verde, N. Ticozzi
Amyotrophic lateral sclerosis: Genotypes and phenotypes
2014 N. Ticozzi, V. Silani
An eye-tracker controlled cognitive battery : overcoming verbal-motor limitations in ALS
2017 B. Poletti, L. Carelli, F. Solca, A. Lafronza, E. Pedroli, A. Faini, N. Ticozzi, A. Ciammola, P. Meriggi, P. Cipresso, D. Lulé, A.C. Ludolph, G. Riva, V. Silani
An eye-tracking controlled neuropsychological battery for cognitive assessment in neurological diseases
2017 B. Poletti, L. Carelli, F. Solca, A. Lafronza, E. Pedroli, A. Faini, S. Zago, N. Ticozzi, A. Ciammola, C. Morelli, P. Meriggi, P. Cipresso, D. Lulé, A.C. Ludolph, G. Riva, V. Silani
Analysis of FUS Gene Mutation in Familial Amyotrophic Lateral Sclerosis within an Italian cohort
2009 N. Ticozzi, V. Silani, A.L. Leclerc, P. Keagle, C. Gellera, A. Ratti, F. Taroni, T.J. Kwiatkowski, D.M. McKenna Yasek, P.C. Sapp, R.H. Brown, J.E. Landers
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
Analysis of miRNA rare variants in amyotrophic lateral sclerosis and in silico prediction of their biological effects
2022 A. Brusati, A. Ratti, V. Pensato, S. Peverelli, D. Gentilini, E. Dalla Bella, M.N. Sorce, M. Meneri, D. Gagliardi, S. Corti, C. Gellera, G. Lauria Pinter, N. Ticozzi, V. Silani
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
2014 P.T. van Doormaal, N. Ticozzi, C. Gellera, A. Ratti, F. Taroni, A. Chiò, A. Calvo, G. Mora, G. Restagno, B.J. Traynor, A. Birve, R. Lemmens, M.A. van Es, C.G. Saris, H.M. Blauw, P.W. van Vught, E.J. Groen, L. Corrado, L. Mazzini, R. Del Bo, S. Corti, S. Waibel, T. Meyer, A.C. Ludolph, A. Goris, P. van Damme, W. Robberecht, A. Shatunov, I. Fogh, P.M. Andersen, S. D'Alfonso, O. Hardiman, S. Cronin, D. Rujescu, A. Al Chalabi, J.E. Landers, V. Silani, L.H. van den Berg, J.H. Veldink
Angiogenin gene mutations in Italian patients with familial and sporadic ALS
2007 N. Ticozzi, C. Gellera, C. Colombrita, B. Castellotti, C. Bragato, A. Ratti, F. Taroni, V. Silani
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis
2011 M.A. van Es, H.J. Schelhaas, P.W.J. van Vught, N. Ticozzi, P.M. Andersen, E.J.N. Groen, C. Schulte, H.M. Blauw, M. Koppers, F.P. Diekstra, K. Fumoto, A.L. LeClerc, P. Keagle, B.R. Bloem, H. Sheffer, B.F.I. van Nuenen, M. van Blitterswijk, W. van rheenen, A.M. Wills, P.P. Lowe, G. Hu, W. Yu, H. Kishikawa, D. Wu, R.D. Folkerth, C. Mariani, S. Goldwurm, G. Pezzoli, P. Van Damme, R. Lemmers, C. Dahlberg, A. Birve, R. Fernandez-Santiago, S. Waibel, C. Klein, M. Weber, A.J. van der Kooi, M. de Visser, D. Dagmar Verbaa, J.J. van Hilten, P. Heutink, E.A.M. Hennekam,E. Cuppen, D. Berg, R.H. Jr. Brown, V. Silani, T. Gasser, A.C. Ludolph, W. Robberecht, R.A. Ophoff, J.H. Veldink, R.J. Pasterkamp, P.L.W. de Bakker, J.E. Landers, B.P. van de Warrenburg, L.H. van den Berg
Angiogenin: a novel candidate gene for ALS pathogenesis in the Italian Population
2007 C. Colombrita, C. Gellera, N. Ticozzi, B. Castelletti, A. Ratti, C. Bragato, F. Taroni, V. Silani
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis
2016 I. Fogh, K. Lin, C. Tiloca, J. Rooney, C. Gellera, F.P. Diekstra, A. Ratti, A. Shatunov, M.A. van Es, P. Proitsi, A. Jones, W. Sproviero, A. Chiò, R.L. Mclaughlin, G. Sorarù, L. Corrado, D. Stahl, R. Del Bo, C. Cereda, B. Castellotti, J.D. Glass, S. Newhouse, R. Dobson, B.N. Smith, S. Topp, W. van Rheenen, V. Meininger, J. Melki, K.E. Morrison, P.J. Shaw, P.N. Leigh, P.M. Andersen, G.P. Comi, N. Ticozzi, L. Mazzini, S. D'Alfonso, B.J. Traynor, P. Van Damme, W. Robberecht, R.H. Brown, J.E. Landers, O. Hardiman, C.M. Lewis, L.H. van den Berg, C.E. Shaw, J.H. Veldink, V. Silani, A. Al Chalabi, J. Powell