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PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.
Oldoni E, Fumagalli GG, Serpente M, Fenoglio C, Scarioni M, Arighi A, Bruno G, Talarico G, Confaloni A, Piscopo P, Nacmias B, Sorbi S, Rainero I, Rubino E, Pinessi L, Binetti G, Ghidoni R, Benussi L, Grande G, Arosio B, Bursey D, Kauwe JS, Cioffi SM, Arcaro M, Mari D, Mariani C, Scarpini E, Galimberti D. Oldoni E, et al. Among authors: arosio b. J Alzheimers Dis. 2016;50(2):353-7. doi: 10.3233/JAD-150863. J Alzheimers Dis. 2016. PMID: 26757195 Free article.
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, Haines JL, Tognoni G, Fiévet N, Dartigues JF, Tzourio C, Engelborghs S, Arosio B, Coto E, De Deyn P, Del Zompo M, Mateo I, Boada M, Antunez C, Lopez-Arrieta J, Epelbaum J, Schjeide BM, Frank-Garcia A, Giedraitis V, Helisalmi S, Porcellini E, Pilotto A, Forti P, Ferri R, Delepine M, Zelenika D, Lathrop M, Scarpini E, Siciliano G, Solfrizzi V, Sorbi S, Spalletta G, Ravaglia G, Valdivieso F, Vepsäläinen S, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossù P, Hanon O, Piccardi P, Annoni G, Mann D, Marambaud P, Seripa D, Galimberti D, Tanzi RE, Bertram L, Lendon C, Lannfelt L, Licastro F, Campion D, Pericak-Vance MA, Soininen H, Van Broeckhoven C, Alpérovitch A, Ruiz A, Kamboh MI, Amouyel P. Lambert JC, et al. Among authors: arosio b. J Alzheimers Dis. 2010;22(1):247-55. doi: 10.3233/JAD-2010-100933. J Alzheimers Dis. 2010. PMID: 20847397 Free PMC article.
NALP1/NLRP1 genetic variants are associated with Alzheimer disease.
Pontillo A, Catamo E, Arosio B, Mari D, Crovella S. Pontillo A, et al. Among authors: arosio b. Alzheimer Dis Assoc Disord. 2012 Jul-Sep;26(3):277-81. doi: 10.1097/WAD.0b013e318231a8ac. Alzheimer Dis Assoc Disord. 2012. PMID: 21946017
Pin1 contribution to Alzheimer's disease: transcriptional and epigenetic mechanisms in patients with late-onset Alzheimer's disease.
Arosio B, Bulbarelli A, Bastias Candia S, Lonati E, Mastronardi L, Romualdi P, Candeletti S, Gussago C, Galimberti D, Scarpini E, Dell'Osso B, Altamura C, MacCarrone M, Bergamaschini L, D'Addario C, Mari D. Arosio B, et al. Neurodegener Dis. 2012;10(1-4):207-11. doi: 10.1159/000333799. Epub 2012 Jan 17. Neurodegener Dis. 2012. PMID: 22261503
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII.
D'Addario C, Dell'Osso B, Palazzo MC, Benatti B, Lietti L, Cattaneo E, Galimberti D, Fenoglio C, Cortini F, Scarpini E, Arosio B, Di Francesco A, Di Benedetto M, Romualdi P, Candeletti S, Mari D, Bergamaschini L, Bresolin N, Maccarrone M, Altamura AC. D'Addario C, et al. Among authors: arosio b. Neuropsychopharmacology. 2012 Jun;37(7):1647-55. doi: 10.1038/npp.2012.10. Epub 2012 Feb 22. Neuropsychopharmacology. 2012. PMID: 22353757 Free PMC article.
Epigenetic regulation of fatty acid amide hydrolase in Alzheimer disease.
D'Addario C, Di Francesco A, Arosio B, Gussago C, Dell'Osso B, Bari M, Galimberti D, Scarpini E, Altamura AC, Mari D, Maccarrone M. D'Addario C, et al. Among authors: arosio b. PLoS One. 2012;7(6):e39186. doi: 10.1371/journal.pone.0039186. Epub 2012 Jun 12. PLoS One. 2012. PMID: 22720070 Free PMC article.
157 results