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Age at onset reveals different functional connectivity abnormalities in prodromal Alzheimer's disease.
Pini L, Geroldi C, Galluzzi S, Baruzzi R, Bertocchi M, Chitò E, Orini S, Romano M, Cotelli M, Rosini S, Magnaldi S, Morassi M, Cobelli M, Bonvicini C, Archetti S, Zanetti O, Frisoni GB, Pievani M. Pini L, et al. Among authors: bonvicini c. Brain Imaging Behav. 2020 Dec;14(6):2594-2605. doi: 10.1007/s11682-019-00212-6. Brain Imaging Behav. 2020. PMID: 31903525
Promoter haplotypes of interleukin-10 gene and sporadic Alzheimer's disease.
Scassellati C, Zanardini R, Squitti R, Bocchio-Chiavetto L, Bonvicini C, Binetti G, Zanetti O, Cassetta E, Gennarelli M. Scassellati C, et al. Among authors: bonvicini c. Neurosci Lett. 2004 Feb 12;356(2):119-22. doi: 10.1016/j.neulet.2003.11.033. Neurosci Lett. 2004. PMID: 14746878
Possible influence of a non-synonymous polymorphism located in the NGF precursor on susceptibility to late-onset Alzheimer's disease and mild cognitive impairment.
Di Maria E, Giorgio E, Uliana V, Bonvicini C, Faravelli F, Cammarata S, Novello MC, Galimberti D, Scarpini E, Zanetti O, Gennarelli M, Tabaton M. Di Maria E, et al. Among authors: bonvicini c. J Alzheimers Dis. 2012;29(3):699-705. doi: 10.3233/JAD-2012-112006. J Alzheimers Dis. 2012. PMID: 22330829 Free article.
PCLO gene: its role in vulnerability to major depressive disorder.
Minelli A, Scassellati C, Cloninger CR, Tessari E, Bortolomasi M, Bonvicini C, Giacopuzzi M, Frisoni GB, Gennarelli M. Minelli A, et al. Among authors: bonvicini c. J Affect Disord. 2012 Aug;139(3):250-5. doi: 10.1016/j.jad.2012.01.028. Epub 2012 Mar 3. J Affect Disord. 2012. PMID: 22386049
Supporting evidence for using biomarkers in the diagnosis of MCI due to AD.
Galluzzi S, Geroldi C, Amicucci G, Bocchio-Chiavetto L, Bonetti M, Bonvicini C, Cotelli M, Ghidoni R, Paghera B, Zanetti O, Frisoni GB; Translational Outpatient Memory Clinic Working Group. Galluzzi S, et al. Among authors: bonvicini c. J Neurol. 2013 Feb;260(2):640-50. doi: 10.1007/s00415-012-6694-0. Epub 2012 Oct 16. J Neurol. 2013. PMID: 23070466
Heterozygous TREM2 mutations in frontotemporal dementia.
Borroni B, Ferrari F, Galimberti D, Nacmias B, Barone C, Bagnoli S, Fenoglio C, Piaceri I, Archetti S, Bonvicini C, Gennarelli M, Turla M, Scarpini E, Sorbi S, Padovani A. Borroni B, et al. Among authors: bonvicini c. Neurobiol Aging. 2014 Apr;35(4):934.e7-10. doi: 10.1016/j.neurobiolaging.2013.09.017. Epub 2013 Oct 16. Neurobiol Aging. 2014. PMID: 24139279 Free article.
88 results