Works matching AU Tiloca, Cinzia

Results: 15
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    Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

    Published in:
    JAMA Neurology, 2016, v. 73, n. 7, p. 812, doi. 10.1001/jamaneurol.2016.1114
    By:
    • Fogh, Isabella;
    • Kuang Lin;
    • Tiloca, Cinzia;
    • Rooney, James;
    • Gellera, Cinzia;
    • Diekstra, Frank P.;
    • Ratti, Antonia;
    • Shatunov, Aleksey;
    • van Es, Michael A.;
    • Proitsi, Petroula;
    • Jones, Ashley;
    • Sproviero, William;
    • Chiò, Adriano;
    • McLaughlin, Russell Lewis;
    • Sorarù, Gianni;
    • Corrado, Lucia;
    • Stahl, Daniel;
    • Del Bo, Roberto;
    • Cereda, Cristina;
    • Castellotti, Barbara
    Publication type:
    Article
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    4

    Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patients.

    Published in:
    Journal of Neurology, 2025, v. 272, n. 7, p. 1, doi. 10.1007/s00415-025-13153-6
    By:
    • Pensato, Viviana;
    • Peverelli, Silvia;
    • Tiloca, Cinzia;
    • Magri, Stefania;
    • Brusati, Alberto;
    • Pingue, Monica;
    • Morelli, Claudia;
    • Dalla Bella, Eleonora;
    • Manini, Arianna;
    • Tannorella, Pierpaola;
    • Doretti, Alberto;
    • Mandrioli, Jessica;
    • Terenghi, Fabrizia;
    • Prelle, Alessandro;
    • Riva, Nilo;
    • Verde, Federico;
    • Eleopra, Roberto;
    • Taroni, Franco;
    • Lauria Pinter, Giuseppe;
    • Silani, Vincenzo
    Publication type:
    Article
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    Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases.

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2018, v. 19, n. 5/6, p. 426, doi. 10.1080/21678421.2018.1440407
    By:
    • Corrado, Lucia;
    • Locci, Clarissa;
    • Bagarotti, Alessandra;
    • Barizzone, Nadia;
    • Cotella, Diego;
    • D'alfonso, Sandra;
    • Tiloca, Cinzia;
    • Colombrita, Claudia;
    • Ticozzi, Nicola;
    • Ratti, Antonia;
    • Silani, Vincenzo;
    • Hamzeiy, Hamid;
    • Nazli Basak, AYSE;
    • De marchi, Fabiola;
    • Mazzini, Letizia
    Publication type:
    Article
    10

    The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS).

    Published in:
    Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2016, v. 17, n. 7/8/2016, p. 489, doi. 10.1080/21678421.2016.1183679
    By:
    • Poletti, Barbara;
    • Solca, Federica;
    • Carelli, Laura;
    • Madotto, Fabiana;
    • Lafronza, Annalisa;
    • Faini, Andrea;
    • Monti, Alessia;
    • Zago, Stefano;
    • Calini, Daniela;
    • Tiloca, Cinzia;
    • Doretti, Alberto;
    • Verde, Federico;
    • Ratti, Antonia;
    • Ticozzi, Nicola;
    • Abrahams, Sharon;
    • Silani, Vincenzo
    Publication type:
    Article
    11

    The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1.

    Published in:
    Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00064
    By:
    • Perez Carrion, Maria;
    • Pischedda, Francesca;
    • Biosa, Alice;
    • Russo, Isabella;
    • Straniero, Letizia;
    • Civiero, Laura;
    • Guida, Marianna;
    • Gloeckner, Christian J.;
    • Ticozzi, Nicola;
    • Tiloca, Cinzia;
    • Mariani, Claudio;
    • Pezzoli, Gianni;
    • Duga, Stefano;
    • Pichler, Irene;
    • Pan, Lifeng;
    • Landers, John E.;
    • Greggio, Elisa;
    • Hess, Michael W.;
    • Goldwurm, Stefano;
    • Piccoli, Giovanni
    Publication type:
    Article
    12
    13

    Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis.

    Published in:
    Nature, 2012, v. 488, n. 7412, p. 499, doi. 10.1038/nature11280
    By:
    • Wu, Chi-Hong;
    • Fallini, Claudia;
    • Ticozzi, Nicola;
    • Keagle, Pamela J.;
    • Sapp, Peter C.;
    • Piotrowska, Katarzyna;
    • Lowe, Patrick;
    • Koppers, Max;
    • McKenna-Yasek, Diane;
    • Baron, Desiree M.;
    • Kost, Jason E.;
    • Gonzalez-Perez, Paloma;
    • Fox, Andrew D.;
    • Adams, Jenni;
    • Taroni, Franco;
    • Tiloca, Cinzia;
    • Leclerc, Ashley Lyn;
    • Chafe, Shawn C.;
    • Mangroo, Dev;
    • Moore, Melissa J.
    Publication type:
    Article
    14

    The role of de novo mutations in the development of amyotrophic lateral sclerosis.

    Published in:
    Human Mutation, 2017, v. 38, n. 11, p. 1534, doi. 10.1002/humu.23295
    By:
    • Doormaal, Perry T.C.;
    • Ticozzi, Nicola;
    • Weishaupt, Jochen H.;
    • Kenna, Kevin;
    • Diekstra, Frank P.;
    • Verde, Federico;
    • Andersen, Peter M.;
    • Dekker, Annelot M.;
    • Tiloca, Cinzia;
    • Marroquin, Nicolai;
    • Overste, Daniel J.;
    • Pensato, Viviana;
    • Nürnberg, Peter;
    • Pulit, Sara L.;
    • Schellevis, Raymond D.;
    • Calini, Daniela;
    • Altmüller, Janine;
    • Francioli, Laurent C.;
    • Muller, Bernard;
    • Castellotti, Barbara
    Publication type:
    Article
    15

    A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.

    Published in:
    Human Molecular Genetics, 2014, v. 23, n. 8, p. 2220
    By:
    • Fogh, Isabella;
    • Ratti, Antonia;
    • Gellera, Cinzia;
    • Lin, Kuang;
    • Tiloca, Cinzia;
    • Moskvina, Valentina;
    • Corrado, Lucia;
    • Sorarù, Gianni;
    • Cereda, Cristina;
    • Corti, Stefania;
    • Gentilini, Davide;
    • Calini, Daniela;
    • Castellotti, Barbara;
    • Mazzini, Letizia;
    • Querin, Giorgia;
    • Gagliardi, Stella;
    • Del Bo, Roberto;
    • Conforti, Francesca L.;
    • Siciliano, Gabriele;
    • Inghilleri, Maurizio
    Publication type:
    Article