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703 results

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Page 1
Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.
Fenoglio C, Galimberti D, Cortini F, Kauwe JS, Cruchaga C, Venturelli E, Villa C, Serpente M, Scalabrini D, Mayo K, Piccio LM, Clerici F, Albani D, Mariani C, Forloni G, Bresolin N, Goate AM, Scarpini E. Fenoglio C, et al. Among authors: villa c. J Alzheimers Dis. 2009;18(3):603-12. doi: 10.3233/JAD-2009-1170. J Alzheimers Dis. 2009. PMID: 19625741 Free PMC article.
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.
Scalabrini D, Fenoglio C, Scarpini E, De Riz M, Comi C, Venturelli E, Cortini F, Piola M, Villa C, Naldi P, Monaco F, Bresolin N, Galimberti D. Scalabrini D, et al. Among authors: villa c. Neurosci Lett. 2007 Oct 2;425(3):173-6. doi: 10.1016/j.neulet.2007.08.020. Epub 2007 Aug 17. Neurosci Lett. 2007. PMID: 17825989
Novel exon 1 progranulin gene variant in Alzheimer's disease.
Cortini F, Fenoglio C, Guidi I, Venturelli E, Pomati S, Marcone A, Scalabrini D, Villa C, Clerici F, Dalla Valle E, Mariani C, Cappa S, Bresolin N, Scarpini E, Galimberti D. Cortini F, et al. Among authors: villa c. Eur J Neurol. 2008 Oct;15(10):1111-7. doi: 10.1111/j.1468-1331.2008.02266.x. Epub 2008 Aug 26. Eur J Neurol. 2008. PMID: 18752597
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Ghidoni R, Cortini F, Scalabrini D, Gallone S, Rainero I, Mandelli A, Restelli I, Binetti G, Cappa S, Mariani C, Giordana MT, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: villa c. Eur J Neurol. 2009 Jan;16(1):37-42. doi: 10.1111/j.1468-1331.2008.02335.x. Eur J Neurol. 2009. PMID: 19087148
Candidate gene analysis of selectin cluster in patients with multiple sclerosis.
Fenoglio C, Scalabrini D, Piccio L, De Riz M, Venturelli E, Cortini F, Villa C, Serpente M, Parks B, Rinker J, Cross AH, Bresolin N, Scarpini E, Galimberti D. Fenoglio C, et al. Among authors: villa c. J Neurol. 2009 May;256(5):832-3. doi: 10.1007/s00415-009-5016-7. Epub 2009 Feb 25. J Neurol. 2009. PMID: 19240957
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
Villa C, Venturelli E, Fenoglio C, Clerici F, Marcone A, Benussi L, Gallone S, Scalabrini D, Cortini F, Serpente M, Martinelli Boneschi F, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Eur J Neurol. 2009 Jul;16(7):870-3. doi: 10.1111/j.1468-1331.2009.02611.x. Epub 2009 Mar 31. Eur J Neurol. 2009. PMID: 19473369
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels.
Galimberti D, Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Cortini F, Scalabrini D, Perini L, Restelli I, Binetti G, Cappa S, Mariani C, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: villa c. J Alzheimers Dis. 2009;17(1):125-33. doi: 10.3233/JAD-2009-1019. J Alzheimers Dis. 2009. PMID: 19494437
703 results