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430 results
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Page 1
Late-onset presentation and phenotypic heterogeneity of the rare R377W PSEN1 mutation.
Scarioni M, Arighi A, Fenoglio C, Sorrentino F, Serpente M, Rotondo E, Mercurio M, Marotta G, Dijkstra AA, Pijnenburg YAL, Scarpini E, Galimberti D. Scarioni M, et al. Among authors: fenoglio c. Eur J Neurol. 2020 Dec;27(12):2630-2634. doi: 10.1111/ene.14506. Epub 2020 Oct 12. Eur J Neurol. 2020. PMID: 32894632 Free article.
Amyloid PET as a marker of normal-appearing white matter early damage in multiple sclerosis: correlation with CSF β-amyloid levels and brain volumes.
Pietroboni AM, Carandini T, Colombi A, Mercurio M, Ghezzi L, Giulietti G, Scarioni M, Arighi A, Fenoglio C, De Riz MA, Fumagalli GG, Basilico P, Serpente M, Bozzali M, Scarpini E, Galimberti D, Marotta G. Pietroboni AM, et al. Among authors: fenoglio c. Eur J Nucl Med Mol Imaging. 2019 Feb;46(2):280-287. doi: 10.1007/s00259-018-4182-1. Epub 2018 Oct 21. Eur J Nucl Med Mol Imaging. 2019. PMID: 30343433
Monozygotic Twins with Frontotemporal Dementia Due To Thr272fs GRN Mutation Discordant for Age At Onset.
Fumagalli GG, Sacchi L, Basilico P, Arighi A, Carandini T, Scarioni M, Colombi A, Pietroboni A, Ghezzi L, Fenoglio C, Serpente M, D'anca M, Arcaro M, Mercurio M, Triulzi F, Scola E, Marotta G, Scarpini E, Galimberti D. Fumagalli GG, et al. Among authors: fenoglio c. J Alzheimers Dis. 2019;67(4):1173-1179. doi: 10.3233/JAD-180723. J Alzheimers Dis. 2019. PMID: 30689572
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: fenoglio 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
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: fenoglio c. 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
The CST3 B haplotype is associated with frontotemporal lobar degeneration.
Benussi L, Ghidoni R, Galimberti D, Boccardi M, Fenoglio C, Scarpini E, Frisoni GB, Binetti G. Benussi L, et al. Among authors: fenoglio c. Eur J Neurol. 2010 Jan;17(1):143-6. doi: 10.1111/j.1468-1331.2009.02767.x. Epub 2009 Aug 5. Eur J Neurol. 2010. PMID: 19674067
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: fenoglio c. 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
430 results