Sfoglia per Autore
Reconsidering the causality of TIA1 mutations in ALS
2018 R.A. van der Spek, W. van Rheenen, S.L. Pulit, K.P. Kenna, N. Ticozzi, M. Kooyman, R.L. Mclaughlin, M. Moisse, K.R. van Eijk, J.J.F.A. van Vugt, A. Iacoangeli, P. Andersen, A.N. Basak, I. Blair, M. de Carvalho, A. Chio, P. Corcia, P. Couratier, V.E. Drory, J.D. Glass, O. Hardiman, J.S. Mora, K.E. Morrison, M. Mitne-Neto, W. Robberecht, P.J. Shaw, M.P. Panadés, P. van Damme, V. Silani, M. Gotkine, M. Weber, M.A. van Es, J.E. Landers, A. Al-Chalabi, L.H. van den Berg, J.H. Veldink
No C9orf72 repeat expansion in patients with primary progressive multiple sclerosis
2018 C. Tiloca, M. Sorosina, F. Esposito, S. Peroni, C. Colombrita, N. Ticozzi, A. Ratti, F. Martinelli Boneschi, V. Silani
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1
2018 M. Perez Carrion, F. Pischedda, A. Biosa, I. Russo, L. Straniero, L. Civiero, M. Guida, C.J. Gloeckner, N. Ticozzi, C. Tiloca, C. Mariani, G. Pezzoli, S. Duga, I. Pichler, L. Pan, J.E. Landers, E. Greggio, M.W. Hess, S. Goldwurm, G. Piccoli
Elevated global DNA methylation is not exclusive to amyotrophic lateral sclerosis and is also observed in spinocerebellar ataxia types 1 and 2
2018 H. Hamzeiy, D. Savaş, C. Tunca, N.E. Şen, A. Gündoğdu Eken, I. Şahbaz, D. Calini, C. Tiloca, N. Ticozzi, A. Ratti, V. Silani, A.N. Başak
Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis
2018 J. Mandrioli, L. Ferri, A. Fasano, E. Zucchi, N. Fini, C. Moglia, C. Lunetta, K. Marinou, N. Ticozzi, G.D. Ferrante, C. Scialo, G. Sorarù, F. Trojsi, A. Conte, Y.M. Falzone, R. Tortelli, M. Russo, V.A. Sansone, G. Mora, V. Silani, P. Volanti, C. Caponnetto, G. Querin, M.R. Monsurrò, M. Sabatelli, A. Chiò, N. Riva, G. Logroscino, S. Messina, A. Calvo
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
The complex interplay between depression/anxiety and executive functioning : insights from the ECAS in a large ALS Population
2018 L. Carelli, F. Solca, A. Faini, F. Madotto, A. Lafronza, A. Monti, S. Zago, A. Doretti, A. Ciammola, N. Ticozzi, V. Silani, B. Poletti
Characterization of the c9orf72 GC-rich low complexity sequence in two cohorts of Italian and Turkish ALS cases
2018 L. Corrado, C. Tiloca, C. Locci, A. Bagarotti, H. Hamzeiy, C. Colombrita, F. De marchi, N. Barizzone, D. Cotella, N. Ticozzi, L. Mazzini, A. Nazli Basak, A. Ratti, V. Silani, S. D’Alfonso
Identification of new HSPB8 variants linked to familial Amiotrophic Lateral Sclerosis
2018 V. Crippa, B. Tedesco, M.E. Cicardi, P. Rusmini, R. Cristofani, V. Ferrari, G. Vezzoli, M. Meroni, E. Messi, M. Piccolella, M. Galbiati, N. Ticozzi, A. Ratti, V. Silani, A.D. Carrà, I. Bigi, L. Mediani, F.F. Morelli, S. Carra, A. Poletti
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
Sexuality and intimacy in ALS: systematic literature review and future perspectives
2018 B. Poletti, L. Carelli, F. Solca, R. Pezzati, A. Faini, N. Ticozzi, H. Mitsumoto, V. Silani
Response to the commentary “The effect of C9orf72 intermediate repeat expansions in neurodegenerative and autoimmune diseases” by Biasiotto G and Zanella I.
2019 C. Tiloca, M. Sorosina, F. Esposito, S. Peroni, C. Colombrita, N. Ticozzi, A. Ratti, F.M. Boneschi, V. Silani
Psychiatric Symptoms in Amyotrophic Lateral Sclerosis : Beyond a Motor Neuron Disorder
2019 E. Zucchi, N. Ticozzi, J. Mandrioli
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
Comparative Analysis of C9orf72 and Sporadic Disease in a Large Multicenter ALS Population: The Effect of Male Sex on Survival of C9orf72 Positive Patients
2019 F. Trojsi, M. Siciliano, C. Femiano, G. Santangelo, C. Lunetta, A. Calvo, C. Moglia, K. Marinou, N. Ticozzi, C. Ferro, C. Scialò, G. Sorarù, A. Conte, Y.M. Falzone, R. Tortelli, M. Russo, V.A. Sansone, A. Chiò, G. Mora, V. Silani, P. Volanti, C. Caponnetto, G. Querin, M. Sabatelli, N. Riva, G. Logroscino, S. Messina, A. Fasano, M.R. Monsurrò, G. Tedeschi, J. Mandrioli
TDP-43 real-time quaking induced conversion reaction optimization and detection of seeding activity in CSF of amyotrophic lateral sclerosis and frontotemporal dementia patients
2020 C. Scialò, T.H. Tran, G. Salzano, G. Novi, C. Caponnetto, A. Chiò, A. Calvo, A. Canosa, F. Moda, P. Caroppo, V. Silani, N. Ticozzi, A. Ratti, B. Borroni, L. Benussi, R. Ghidoni, G. Furlanis, P. Manganotti, B. Senigagliesi, P. Parisse, R. Brasselet, E. Buratti, G. Legname
Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis
2020 C. Carlomagno, P.I. Banfi, A. Gualerzi, S. Picciolini, E. Volpato, M. Meloni, A. Lax, E. Colombo, N. Ticozzi, F. Verde, V. Silani, M. Bedoni
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
Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: OPTN, VCP, and SQSTM1 Variants Account for 3% of Rare Genetic Forms
2020 V. Pensato, S. Magri, E.D. Bella, P. Tannorella, E. Bersano, G. Sorarù, M. Gatti, N. Ticozzi, F. Taroni, G. Lauria, C. Mariotti, C. Gellera
CSF angiogenin levels in amyotrophic lateral Sclerosis-Frontotemporal dementia spectrum
2020 C. Morelli, C. Tiloca, C. Colombrita, A. Zambon, D. Soranna, A. Lafronza, F. Solca, L. Carelli, B. Poletti, A. Doretti, F. Verde, L. Maderna, N. Ticozzi, A. Ratti, V. Silani
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile