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Page 1
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Cortini F, Fumagalli G, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: scalabrini d. Neurosci Lett. 2010 Oct 4;482(3):240-4. doi: 10.1016/j.neulet.2010.07.047. Epub 2010 Jul 27. Neurosci Lett. 2010. PMID: 20670673
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: scalabrini d. 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: scalabrini d. 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
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis.
Fenoglio C, Galimberti D, Ban M, Maranian M, Scalabrini D, Venturelli E, Piccio L, De Riz M, Yeo TW, Goris A, Gray J, Bresolin N, Scarpini E, Compston A, Sawcer S. Fenoglio C, et al. Among authors: scalabrini d. Neurosci Lett. 2006 Feb 13;394(2):92-6. doi: 10.1016/j.neulet.2005.10.014. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257118
Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease.
Venturelli E, Galimberti D, Fenoglio C, Lovati C, Finazzi D, Guidi I, Corrà B, Scalabrini D, Clerici F, Mariani C, Forloni G, Bresolin N, Scarpini E. Venturelli E, et al. Among authors: scalabrini d. Neurosci Lett. 2006 Aug 14;404(1-2):217-21. doi: 10.1016/j.neulet.2006.05.054. Epub 2006 Jun 19. Neurosci Lett. 2006. PMID: 16787707
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. 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
34 results