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Page 1
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.
Ferrari R, Grassi M, Salvi E, Borroni B, Palluzzi F, Pepe D, D'Avila F, Padovani A, Archetti S, Rainero I, Rubino E, Pinessi L, Benussi L, Binetti G, Ghidoni R, Galimberti D, Scarpini E, Serpente M, Rossi G, Giaccone G, Tagliavini F, Nacmias B, Piaceri I, Bagnoli S, Bruni AC, Maletta RG, Bernardi L, Postiglione A, Milan G, Franceschi M, Puca AA, Novelli V, Barlassina C, Glorioso N, Manunta P, Singleton A, Cusi D, Hardy J, Momeni P. Ferrari R, et al. Among authors: serpente m. Neurobiol Aging. 2015 Oct;36(10):2904.e13-26. doi: 10.1016/j.neurobiolaging.2015.06.005. Epub 2015 Jun 12. Neurobiol Aging. 2015. PMID: 26154020 Free PMC article.
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration.
Villa C, Venturelli E, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Cortini F, Scalabrini D, Serpente M, Binetti G, Cappa S, Mariani C, Rainero I, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Among authors: serpente m. J Neurol. 2009 Aug;256(8):1379-81. doi: 10.1007/s00415-009-5138-y. Epub 2009 May 5. J Neurol. 2009. PMID: 19415413
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: serpente m. 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
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: serpente m. 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 semaphorins in patients with Alzheimer's disease.
Villa C, Venturelli E, Fenoglio C, De Riz M, Scalabrini D, Cortini F, Serpente M, Cantoni C, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Among authors: serpente m. Neurol Sci. 2010 Apr;31(2):169-73. doi: 10.1007/s10072-009-0200-1. Epub 2009 Dec 3. Neurol Sci. 2010. PMID: 19957197
GRN variability contributes to sporadic frontotemporal lobar degeneration.
Galimberti D, Fenoglio C, Cortini F, Serpente M, Venturelli E, Villa C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Restelli I, Martinelli Boneschi F, Cappa S, Binetti G, Mariani C, Rainero I, Giordana MT, Bresolin N, Scarpini E. Galimberti D, et al. Among authors: serpente m. J Alzheimers Dis. 2010;19(1):171-7. doi: 10.3233/JAD-2010-1225. J Alzheimers Dis. 2010. PMID: 20061636
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort.
Martinelli-Boneschi F, Esposito F, Scalabrini D, Fenoglio C, Rodegher ME, Brambilla P, Colombo B, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, De Riz M, Serpente M, Cantoni C, Scarpini E, Martinelli V, Galimberti D, Comi G. Martinelli-Boneschi F, et al. Among authors: serpente m. Eur J Neurol. 2010 May;17(5):740-5. doi: 10.1111/j.1468-1331.2009.02925.x. Epub 2010 Jan 7. Eur J Neurol. 2010. PMID: 20067515
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease.
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Cortini F, Serpente M, Cantoni C, Fumagalli G, Ridolfi E, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: serpente m. J Alzheimers Dis. 2011;23(4):701-7. doi: 10.3233/JAD-2010-101416. J Alzheimers Dis. 2011. PMID: 21157029
Phenotypic heterogeneity of the GRN Asp22fs mutation in a large Italian kindred.
Pietroboni AM, Fumagalli GG, Ghezzi L, Fenoglio C, Cortini F, Serpente M, Cantoni C, Rotondo E, Corti P, Carecchio M, Bassi M, Bresolin N, Galbiati D, Galimberti D, Scarpini E. Pietroboni AM, et al. Among authors: serpente m. J Alzheimers Dis. 2011;24(2):253-9. doi: 10.3233/JAD-2011-101704. J Alzheimers Dis. 2011. PMID: 21258152
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: serpente m. 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
109 results