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

984 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Discovering the Italian phenotype of cerebral amyloid angiopathy (CAA): the SENECA project.
Bersano A, Scelzo E, Pantoni L, Morotti A, Erbetta A, Chiapparini L, Vitali P, Giaccone G, Caroppo P, Catania M, Obici L, Di Fede G, Gatti L, Tinelli F, Di Francesco JC, Piazza F, Ferrarese C, Gasparini M, Adobbati L, Bianchi-Marzoli S, Tremolada G, Sacco S, Mancuso M, Zedde ML, Godani M, Lanfranconi S, Pareyson D, Di Girolamo M, Motto C, Charidimou A, Boulouis G, Parati EA; SENECA project. Bersano A, et al. Among authors: giaccone g. Neurol Sci. 2020 Aug;41(8):2193-2200. doi: 10.1007/s10072-020-04306-8. Epub 2020 Mar 12. Neurol Sci. 2020. PMID: 32166471
Conversion of the BASE prion strain into the BSE strain: the origin of BSE?
Capobianco R, Casalone C, Suardi S, Mangieri M, Miccolo C, Limido L, Catania M, Rossi G, Di Fede G, Giaccone G, Bruzzone MG, Minati L, Corona C, Acutis P, Gelmetti D, Lombardi G, Groschup MH, Buschmann A, Zanusso G, Monaco S, Caramelli M, Tagliavini F. Capobianco R, et al. Among authors: giaccone g. PLoS Pathog. 2007 Mar;3(3):e31. doi: 10.1371/journal.ppat.0030031. PLoS Pathog. 2007. PMID: 17352534 Free PMC article.
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1379-82. doi: 10.1136/jnnp.2007.115444. J Neurol Neurosurg Psychiatry. 2007. PMID: 18024694 Free PMC article.
Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.
Bugiani O, Giaccone G, Rossi G, Mangieri M, Capobianco R, Morbin M, Mazzoleni G, Cupidi C, Marcon G, Giovagnoli A, Bizzi A, Di Fede G, Puoti G, Carella F, Salmaggi A, Romorini A, Patruno GM, Magoni M, Padovani A, Tagliavini F. Bugiani O, et al. Among authors: giaccone g. Arch Neurol. 2010 Aug;67(8):987-95. doi: 10.1001/archneurol.2010.178. Arch Neurol. 2010. PMID: 20697050
A novel phenotype of sporadic Creutzfeldt-Jakob disease.
Giaccone G, Di Fede G, Mangieri M, Limido L, Capobianco R, Suardi S, Grisoli M, Binelli S, Fociani P, Bugiani O, Tagliavini F. Giaccone G, et al. BMJ Case Rep. 2009;2009:bcr09.2008.0945. doi: 10.1136/bcr.09.2008.0945. Epub 2009 Feb 2. BMJ Case Rep. 2009. PMID: 21686549 Free PMC article.
984 results