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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

457 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Benussi L, Ghidoni R, Gallone S, Scalabrini D, Cortini F, Fumagalli G, Cappa S, Binetti G, Franceschi M, Rainero I, Giordana MT, Mariani C, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: fenoglio c. Neurosci Lett. 2010 Oct 4;482(3):240-4. doi: 10.1016/j.neulet.2010.07.047. Epub 2010 Jul 27. Neurosci Lett. 2010. PMID: 20670673
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
Venturelli E, Villa C, Fenoglio C, Clerici F, Marcone A, Ghidoni R, Cortini F, Scalabrini D, Gallone S, Rainero I, Mandelli A, Restelli I, Binetti G, Cappa S, Mariani C, Giordana MT, Bresolin N, Scarpini E, Galimberti D. Venturelli E, et al. Among authors: fenoglio c. Eur J Neurol. 2009 Jan;16(1):37-42. doi: 10.1111/j.1468-1331.2008.02335.x. Eur J Neurol. 2009. PMID: 19087148
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
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis.
Fenoglio C, Galimberti D, Ban M, Maranian M, Scalabrini D, Venturelli E, Piccio L, De Riz M, Yeo TW, Goris A, Gray J, Bresolin N, Scarpini E, Compston A, Sawcer S. Fenoglio C, et al. Neurosci Lett. 2006 Feb 13;394(2):92-6. doi: 10.1016/j.neulet.2005.10.014. Epub 2005 Oct 27. Neurosci Lett. 2006. PMID: 16257118
Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease.
Venturelli E, Galimberti D, Fenoglio C, Lovati C, Finazzi D, Guidi I, Corrà B, Scalabrini D, Clerici F, Mariani C, Forloni G, Bresolin N, Scarpini E. Venturelli E, et al. Among authors: fenoglio c. Neurosci Lett. 2006 Aug 14;404(1-2):217-21. doi: 10.1016/j.neulet.2006.05.054. Epub 2006 Jun 19. Neurosci Lett. 2006. PMID: 16787707
457 results