Human salivary Raman fingerprint as biomarker for the diagnosis of Amyotrophic Lateral Sclerosis von Carlomagno, C., Banfi, P. I., Gualerzi, A., Picciolini, S., Volpato, E., Meloni, M., Lax, A., Colombo, E., Ticozzi, N., Verde, F., Silani, V., Bedoni, M.

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Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis von Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr

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Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis von Ticozzi, N., Vance, C., LeClerc, A.L., Keagle, P., Glass, J.D., McKenna-Yasek, D., Sapp, P.C., Silani, V., Bosco, D.A., Shaw, C.E., Brown Jr, R.H., Landers, J.E.

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High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis von Corrado, Lucia, Ratti, A., Gellera, C., Buratti, E., Castellotti, B., Carlomagno, Y., Ticozzi, N., Mazzini, L., Testa, L., Taroni, F., Baralle, F. E., Silani, V., D'Alfonso, S.

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Cardiovascular diseases may play a negative role in the prognosis of amyotrophic lateral sclerosis von Mandrioli, J., Ferri, L., Fasano, A., Zucchi, E., Fini, N., Moglia, C., Lunetta, C., Marinou, K., Ticozzi, N., Drago Ferrante, G., Scialo, C., Sorarù, G., Trojsi, F., Conte, A., Falzone, Y. M., Tortelli, R., Russo, M., Sansone, V. A., Mora, G., Silani, V., Volanti, P., Caponnetto, C., Querin, G., Monsurrò, M. R., Sabatelli, M., Chiò, A., Riva, N., Logroscino, G., Messina, S., Calvo, A.

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Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis von Del Bo, R, Tiloca, C, Pensato, V, Corrado, L, Ratti, A, Ticozzi, N, Corti, S, Castellotti, B, Mazzini, L, Sorarù, G, Cereda, C, D'Alfonso, S, Gellera, C, Comi, G P, Silani, V

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Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort von TICOZZI, N, SILANI, V, BROWN, R. H, LANDERS, J. E, LECLERC, A. L, KEAGLE, P, GELLERA, C, RATTI, A, TARONI, F, KWIATKOWSKI, T. J, MCKENNA-YASEK, D. M, SAPP, P. C

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VPS54 genetic analysis in ALS Italian cohort von Corrado, L., Gagliardi, S., Carlomagno, Y., Mennini, T., Ticozzi, N., Mazzini, L., Silani, V., Cereda, C., D'Alfonso, S.

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Cerebral Amyloid Angiopathy-Related Inflammation: An Emerging Disease von Savoiardo, M., Erbetta, A., Di Francesco, J.C., Brioschi, M., Silani, V., Falini, A., Storchi, G., Brighina, L., Ferrarese, C., Ticozzi, N., Messina, S., Girotti, F.

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EE48 Healthcare Resource Utilization (HCRU), Quality of Life (QoL), and Employment Changes for Early, Middle and Late-Stage People with Amyotrophic Lateral Sclerosis (pALS) in Ital... von Stenson, K., Guerrieri, E., Santoni, L., Mellor, J., Wright, J., Earl, L., Ball, N., Iqbal, H., Thomas, O., Barlow, S., Ticozzi, N.

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Association of Vascular Risk Factors and Cerebrovascular Pathology With Alzheimer Disease Pathologic Changes in Individuals Without Dementia von Lorenzini, Luigi, Maranzano, Alessio, Ingala, Silvia, Collij, Lyduine E, Tranfa, Mario, Blennow, Kaj, Di Perri, Carol, Foley, Christopher, Fox, Nick C, Frisoni, Giovanni B, Haller, Sven, Martinez-Lage, Pablo, Mollison, Daisy, O'Brien, John, Payoux, Pierre, Ritchie, Craig, Scheltens, Philip, Schwarz, Adam J, Sudre, Carole H, Tijms, Betty M, Verde, Federico, Ticozzi, Nicola, Silani, Vincenzo, Visser, Pieter Jelle, Waldman, Adam, Wolz, Robin, Chételat, Gael, Ewers, Michael, Wink, Alle Meije, Mutsaerts, Henk, Gispert, Juan Domingo, Wardlaw, Joanna M, Barkhof, Frederik

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ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function von De Majo, M, Topp, SD, Smith, BN, Nishimura, AL, Chen, HJ, Soragia Gkazi, A, Wong, CH, Vance, C, Bass, F, Ten Ashbroek, ALMA, Kenna, KP, Ticozzi, N, Garcia Redondo, A, Esteban-Perez, J, Tiloca, C, Verde, F, Duga, S, Morrison, KE, Shaw, PJ, Kirby, J, Turner, MR, Talbot, K, Hardiman, O, Glass, JD, De Belleroche, JS, Gellera, C, Ratti, A, Al-Chalabi, A, Silani, V, Landers, JE, Shaw, C

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis von Smith, BN, Topp, SD, Fallini, C, Shibata, H, Chen, H-J, Troakes, C, King, A, Ticozzi, N, Kenna, KP, Soragia-Gkazi, A, Miller, JW, Sato, A, Dias, DM, Jeon, M, Vance, C, Wong, CH, De Majo, M, Kattuah, W, Mitchell, JC, Scotter, EL, Parkin, NW, Sapp, PC, Nolan, M, Nestor, PJ, Simpson, M, Weale, M, Lek, M, Baas, F, De Jong, JMV, Ten Asbroek, ALMA, Garcia Redondo, A, Esteban-Perez, J, Tiloca, C, Verde, F, Duga, S, Leigh, N, Pall, H, Morrison, KE, Al-Chalabi, A, Shaw, PJ, Kirby, J, Turner, MR, Talbot, K, Hardiman, O, Glass, JD, De Belleroche, J, Maki, M, Moss, SE, Miller, C, Gellera, C, Ratti, A, Al-Sarraj, S, Brown, RH, Silani, V, Landers, JE, Shaw, CE

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VPS54 genetic analysis in ALS Italian cohort: Letter to the Editor von Corrado, L., Gagliardi, S., Carlomagno, Y., Mennini, T., Ticozzi, N., Mazzini, L., Silani, V., Cereda, C., D’Alfonso, S.

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Genetics of Amyotrophic Lateral Sclerosis von Kenna, K.P, Landers, J.E, Ticozzi, N

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Molecular and Cellular Therapies for Motor Neuron Diseases von Boulis, Nicholas M, O'Connor, Deirdre, Donsante, Anthony

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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis von Kenna, KP, Van Doormaal, PTC, Dekker, AM, Ticozzi, N, Kenna, BJ, Diekstra, FP, Van Rheenen, W, Van Eijk, KR, Jones, AR, Keagle, P, Shatunov, A, Sproviero, W, Smith, BN, Van Es, MA, Topp, SD, Kenna, A, Miller, JW, Fallini, C, Tiloca, C, McLaughlin, RL, Vance, C, Troakes, C, Colombrita, C, Mora, G, Calvo, A, Verde, F, Al-Sarraj, S, King, A, Calini, D, De Belleroche, J, Baas, F, Van der Kooi, AJ, De Visser, M, Ten Asbroek, ALMA, Sapp, PC, McKenna-Yasek, D, Polak, M, Asress, S, Munoz-Blanco, JL, Strom, TM, Meitinger, T, Morrison, KE, SLAGEN COnsortium, Lauria, G, Williams, KL, Leigh, PN, Nicholson, GA, Blair, IP, Leblond, CS, Dion, PA, Rouleau, GA, Pall, H, Shaw, PJ, Turner, MR, Talbot, K, Taroni, F, Boylan, KB, Van Blitterswijk, M, Rademakers, R, Esteban-Perez, J, Garcia-Redondo, A, Van Damme, P, Robberecht, W, Chio, A, Gellera, C, Drepper, C, Sendtner, M, Ratti, A, Glass, JD, Mora, JS, Basak, NA, Hardiman, O, Ludolph, AC, Andersen, PM, Weishaupt, JH, Brown Jr, RH, Al-Chalabi, A, Silani, V, Shaw, CE, Van den Berg, LH, Veldink, JH, Landers, JE

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Mutations in the tail and rod domains of the neurofilament heavy‐chain gene increase the risk of ALS von Marriott, H, Spargo, T.P, Al Khleifat, A, Andersen, P.M, Başak, N.A, Cooper‐Knock, J, Corcia, P, Couratier, P, de Carvalho, M, Drory, V, Gotkine, M, Landers, J.E, McLaughlin, R, Pardina, J.S.M, Morrison, K.E, Pinto, S, Shaw, C.E, Shaw, P.J, Silani, V, Ticozzi, N, van Damme, P, van den Berg, L.H, Vourc'h, P, Weber, M, Veldink, J.H, Dobson, R.J, Schwab, P, Al‐Chalabi, A, Iacoangeli, A

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Genetic variability in sporadic amyotrophic lateral sclerosis von Van Daele, S.H, Moisse, M, van Vugt, J.J.F.A, Zwamborn, R.A.J, van der Spek, R, van Rheenen, W, Van Eijk, K, Kenna, K, Corcia, P, Vourc'h, P, Couratier, P, Hardiman, O, McLaughin, R, Gotkine, M, Drory, V, Ticozzi, N, Silani, V, Ratti, A, de Carvalho, M, Mora Pardina, J.S, Povedano, M, Andersen, P.M, Weber, M, Başak, N.A, Shaw, C, Shaw, P.J, Morrison, K.E, Landers, J.E, Glass, J.D, van Es, M.A, van den Berg, L.H, Al-Chalabi, A, Veldink, J, Van Damme, P

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Large-scale analyses of CAV1 and CAV2 suggest their expression is higher in post-mortem ALS brain tissue and affects survival von Adey, B.N, Cooper-Knock, J, Al Khleifat, A, Fogh, I, van Damme, P, Corcia, P, Couratier, P, Hardiman, O, McLaughlin, R, Gotkine, M, Drory, V, Silani, V, Ticozzi, N, Veldink, J.H, van den Berg, L.H, de Carvalho, M, Pinto, S, Mora Pardina, J.S, Povedano Panades, M, Andersen, P.M, Weber, M, Başak, N.A, Shaw, C.E, Shaw, P.J, Morrison, K.E, Landers, J.E, Glass, J.D, Vourc’h, P, Dobson, R.J.B, Breen, G, Al-Chalabi, A, Jones, A.R, Iacoangeli, A

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