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Page 1
MDC/CCL22 intrathecal levels in patients with multiple sclerosis.
Galimberti D, Fenoglio C, Comi C, Scalabrini D, De Riz M, Leone M, Venturelli E, Cortini F, Piola M, Monaco F, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: cortini f. Mult Scler. 2008 May;14(4):547-9. doi: 10.1177/1352458507084268. Epub 2008 Jan 21. Mult Scler. 2008. PMID: 18208895
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: cortini f. 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
GSK3β genetic variability in patients with Multiple Sclerosis.
Galimberti D, Macmurray J, Scalabrini D, Fenoglio C, De Riz M, Comi C, Comings D, Cortini F, Villa C, Serpente M, Cantoni C, Ridolfi E, Fardipoor MH, Leone M, Monaco F, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: cortini f. Neurosci Lett. 2011 Jun 15;497(1):46-8. doi: 10.1016/j.neulet.2011.04.024. Epub 2011 Apr 17. Neurosci Lett. 2011. PMID: 21527318
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: cortini f. Eur J Neurol. 2009 Jan;16(1):37-42. doi: 10.1111/j.1468-1331.2008.02335.x. Eur J Neurol. 2009. PMID: 19087148
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. Among authors: cortini f. 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
Repetitive element hypermethylation in multiple sclerosis patients.
Neven KY, Piola M, Angelici L, Cortini F, Fenoglio C, Galimberti D, Pesatori AC, Scarpini E, Bollati V. Neven KY, et al. Among authors: cortini f. BMC Genet. 2016 Jun 18;17(1):84. doi: 10.1186/s12863-016-0395-0. BMC Genet. 2016. PMID: 27317098 Free PMC article.
Association of a NOS1 promoter repeat with Alzheimer's disease.
Galimberti D, Scarpini E, Venturelli E, Strobel A, Herterich S, Fenoglio C, Guidi I, Scalabrini D, Cortini F, Bresolin N, Lesch KP, Reif A. Galimberti D, et al. Among authors: cortini f. Neurobiol Aging. 2008 Sep;29(9):1359-65. doi: 10.1016/j.neurobiolaging.2007.03.003. Epub 2007 Apr 6. Neurobiol Aging. 2008. PMID: 17418914
45 results