Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

156 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Whole-genome sequencing analysis of semi-supercentenarians.
Garagnani P, Marquis J, Delledonne M, Pirazzini C, Marasco E, Kwiatkowska KM, Iannuzzi V, Bacalini MG, Valsesia A, Carayol J, Raymond F, Ferrarini A, Xumerle L, Collino S, Mari D, Arosio B, Casati M, Ferri E, Monti D, Nacmias B, Sorbi S, Luiselli D, Pettener D, Castellani G, Sala C, Passarino G, De Rango F, D'Aquila P, Bertamini L, Martinelli N, Girelli D, Olivieri O, Giuliani C, Descombes P, Franceschi C. Garagnani P, et al. Among authors: arosio b. Elife. 2021 May 4;10:e57849. doi: 10.7554/eLife.57849. Elife. 2021. PMID: 33941312 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
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.
Phenotypic variability associated with the C9ORF72 hexanucleotide repeat expansion: a sporadic case of frontotemporal lobar degeneration with prodromal hyposmia and predominant semantic deficits.
Abbate C, Arosio B, Galimberti D, Nicolini P, Chiara LR, Rossi PD, Ferri E, Gussago C, Deriz M, Fenoglio C, Serpente M, Scarpini E, Mari D. Abbate C, et al. Among authors: arosio b. J Alzheimers Dis. 2014;40(4):849-55. doi: 10.3233/JAD-132075. J Alzheimers Dis. 2014. PMID: 24531155 Free article.
156 results