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367 results
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TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations.
Pensato V, Tiloca C, Corrado L, Bertolin C, Sardone V, Del Bo R, Calini D, Mandrioli J, Lauria G, Mazzini L, Querin G, Ceroni M, Cantello R, Corti S, Castellotti B, Soldà G, Duga S, Comi GP, Cereda C, Sorarù G, D'Alfonso S, Taroni F, Shaw CE, Landers JE, Ticozzi N, Ratti A, Gellera C, Silani V; SLAGEN Consortium. Pensato V, et al. Among authors: taroni f. J Neurol. 2015 May;262(5):1376-8. doi: 10.1007/s00415-015-7739-y. Epub 2015 Apr 18. J Neurol. 2015. PMID: 25893256 Free PMC article. No abstract available.
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation.
Di Bella D, Pareyson D, Savoiardo M, Farina L, Ciano C, Caldarazzo S, Sagnelli A, Bonato S, Nava S, Bresolin N, Tedeschi G, Taroni F, Salsano E. Di Bella D, et al. Among authors: taroni f. Neurology. 2014 Sep 23;83(13):1217-8. doi: 10.1212/WNL.0000000000000812. Epub 2014 Aug 15. Neurology. 2014. PMID: 25128180 No abstract available.
Schizencephaly: clinical spectrum, epilepsy, and pathogenesis.
Granata T, Freri E, Caccia C, Setola V, Taroni F, Battaglia G. Granata T, et al. Among authors: taroni f. J Child Neurol. 2005 Apr;20(4):313-8. doi: 10.1177/08830738050200040801. J Child Neurol. 2005. PMID: 15921232 Review.
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