Papers authored by Nicola Ticozzi
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Amyotrophic Lateral Sclerosis: Epidemiology and Risk Factors
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R. A. A. Van Der Spek
and 190 other authors
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Federica Solca,
Laura Carelli,
Fabiana Madotto,
Annalisa Lafronza,
Andrea Faini ,
Alessia Monti,
Stefano Zago,
Daniela Calini,
Cinzia Tiloca,
Alberto Doretti,
Federico Verde,
Antonia Ratti,
Nicola Ticozzi ,
Sharon Abrahams
and 1 other authors
The validation of the Italian Edinburgh Cognitive and Behavioural ALS Screen (ECAS)
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Brendan J. Kenna,
Frank P. Diekstra,
Wouter van Rheenen,
Kristel R. van Eijk,
Ashley R. Jones,
Pamela Keagle,
Aleksey Shatunov,
William Sproviero ,
Bradley N. Smith ,
Michael A. van Es,
Simon D. Topp
and 83 other authors
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
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Caroline Vance ,
Emma L. Scotter ,
Claire Troakes ,
Chun Hao Wong,
Simon Topp ,
Satomi Maekawa,
Andrew King,
Jacqueline C. Mitchell,
Karan Lund ,
Ammar Al-Chalabi,
Nicola Ticozzi ,
Vincenzo Silani,
Peter Sapp,
Robert H. Brown
and 3 other authors
Novel mutations support a role for Profilin 1 in the pathogenesis of ALS
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Lh van den Berg,
Nicola Ticozzi ,
Claudia Fallini,
As Gkazi,
Simon Topp ,
Kp Kenna,
El Scotter ,
Jw Miller,
Jason Kost,
Ew Danielson,
Pamela Keagle,
Ea Lewis,
Daniela Calini,
Anneloor Lma Ten Asbroek
and 80 other authors
Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS.
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Agata Lax,
Giulia Andrea Guidugli,
Antonello Nicolini,
Vincenzo Silani
A Review of Options for Treating Sialorrhea in Amyotrophic Lateral Sclerosis
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Cinzia Gellera ,
Antonia Ratti,
Franco Taroni,
Adriano Chio,
Andrea Calvo,
Gabriele Mora,
Gabriella Restagno,
Bryan J. Traynor,
Anna Birve,
Robin Lemmens,
Michael A. van Es,
Christiaan G. J. Saris
and 30 other authors
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study
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Cinzia Tiloca,
Daniela Calini,
Stella Gagliardi,
Alessandra Altieri,
Claudia Colombrita,
Cristina Cereda,
Antonia Ratti,
Gianni Pezzoli,
Barbara Borroni,
Stefano Goldwurm,
Alessandro Padovani,
Vincenzo Silani
C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
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Letizia Mazzini,
Pamela Milani,
Barbara Castellotti,
Cinzia Bertolin,
Gianni Sorarù,
Cristina Cereda,
Comi Gp,
Giacomo P. Comi
and 8 other authors
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis
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Viviana Pensato,
Lucia Corrado,
Roberto Del Bo,
Cinzia Bertolin,
Chiara Fenoglio,
Stella Gagliardi,
Daniela Calini,
Giuseppe Lauria,
Barbara Castellotti,
Alessandra Bagarotti,
Stefania Corti ,
Daniela Galimberti,
Annachiara Cagnin
and 14 other authors
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia
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Cinzia Tiloca,
Roberto Del Bo,
Lucia Corrado,
Viviana Pensato,
Jennifer Agostini,
Cristina Cereda,
Antonia Ratti,
Barbara Castellotti,
Stefania Corti ,
Alessandra Bagarotti,
Annachiara Cagnin,
Pamela Milani,
Carlo Gabelli,
Giulietta Riboldi
and 8 other authors
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C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
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Nicola Ticozzi ,
Pamela J. Keagle,
Peter C. Sapp,
Katarzyna Piotrowska,
Max Koppers,
Patrick Lowe,
Diane McKenna-Yasek,
Desiree M. Baron,
Jason E. Kost,
Paloma Gonzalez-Perez,
Andrew D. Fox,
Jenni Adams,
Franco Taroni
and 23 other authors
Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis
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Cinzia Tiloca,
Ne Mencacci,
Claudia Morelli,
Alberto Doretti,
Daniela Rusconi,
Claudia Colombrita,
Davide Sangalli,
Federico Verde,
Palma Finelli,
Stefano Messina,
Antonia Ratti,
Vincenzo Silani
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Stephen Newhouse,
Aleksey Shatunov,
Caroline Vance ,
Simon Topp ,
Lauren Johnson,
Jack Miller,
Younbok Lee,
Claire Troakes ,
Kirsten M. Scott,
Ashley Jones,
Ian Gray,
Jamie Wright,
Tibor Hortobágyi,
Safa Al-Sarraj
and 32 other authors
The C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
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