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Page 1
PEN-2 gene mutation in a familial Alzheimer's disease case.
Sala Frigerio C, Piscopo P, Calabrese E, Crestini A, Malvezzi Campeggi L, Civita di Fava R, Fogliarino S, Albani D, Marcon G, Cherchi R, Piras R, Forloni G, Confaloni A. Sala Frigerio C, et al. Among authors: fogliarino s. J Neurol. 2005 Sep;252(9):1033-6. doi: 10.1007/s00415-005-0799-7. Epub 2005 Mar 16. J Neurol. 2005. PMID: 16170650
MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.
Fenoglio C, Galimberti D, Lovati C, Guidi I, Gatti A, Fogliarino S, Tiriticco M, Mariani C, Forloni G, Pettenati C, Baron P, Conti G, Bresolin N, Scarpini E. Fenoglio C, et al. Among authors: fogliarino s. Neurobiol Aging. 2004 Oct;25(9):1169-73. doi: 10.1016/j.neurobiolaging.2003.11.008. Neurobiol Aging. 2004. PMID: 15312962
Pure spastic paraparesis associated with a novel presenilin 1 R278K mutation.
Assini A, Terreni L, Borghi R, Giliberto L, Piccini A, Loqui D, Fogliarino S, Forloni G, Tabaton M. Assini A, et al. Among authors: fogliarino s. Neurology. 2003 Jan 14;60(1):150. doi: 10.1212/01.wnl.0000040252.43269.83. Neurology. 2003. PMID: 12525746 No abstract available.