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Page 1
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: galimberti d. 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
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: galimberti d. J Alzheimers Dis. 2009;18(3):603-12. doi: 10.3233/JAD-2009-1170. J Alzheimers Dis. 2009. PMID: 19625741 Free PMC article.
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease.
Carecchio M, Fenoglio C, De Riz M, Guidi I, Comi C, Cortini F, Venturelli E, Restelli I, Cantoni C, Bresolin N, Monaco F, Scarpini E, Galimberti D. Carecchio M, et al. Among authors: galimberti d. J Neurol Sci. 2009 Dec 15;287(1-2):291-3. doi: 10.1016/j.jns.2009.07.011. Epub 2009 Aug 14. J Neurol Sci. 2009. PMID: 19683260 Free article.
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. 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: galimberti d. 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
Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males.
Fenoglio C, Scalabrini D, Esposito F, Comi C, Cavalla P, De Riz M, Martinelli V, Piccio LM, Venturelli E, Fumagalli G, Capra R, Collimedaglia L, Ghezzi A, Rodegher ME, Vercellino M, Leone M, Giordana MT, Bresolin N, Monaco F, Comi G, Scarpini E, Martinelli-Boneschi F, Galimberti D. Fenoglio C, et al. Among authors: galimberti d. Genes Immun. 2010 Sep;11(6):497-503. doi: 10.1038/gene.2010.18. Epub 2010 May 13. Genes Immun. 2010. PMID: 20463744
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: galimberti d. J Alzheimers Dis. 2011;24(2):253-9. doi: 10.3233/JAD-2011-101704. J Alzheimers Dis. 2011. PMID: 21258152
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
Villa C, Ghezzi L, Pietroboni AM, Fenoglio C, Cortini F, Serpente M, Cantoni C, Ridolfi E, Marcone A, Benussi L, Ghidoni R, Jacini F, Arighi A, Fumagalli GG, Mandelli A, Binetti G, Cappa S, Bresolin N, Scarpini E, Galimberti D. Villa C, et al. Among authors: galimberti d. J Alzheimers Dis. 2011;26(1):19-26. doi: 10.3233/JAD-2011-102124. J Alzheimers Dis. 2011. PMID: 21558644
620 results