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

44 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease.
Collins SJ, Sanchez-Juan P, Masters CL, Klug GM, van Duijn C, Poleggi A, Pocchiari M, Almonti S, Cuadrado-Corrales N, de Pedro-Cuesta J, Budka H, Gelpi E, Glatzel M, Tolnay M, Hewer E, Zerr I, Heinemann U, Kretszchmar HA, Jansen GH, Olsen E, Mitrova E, Alpérovitch A, Brandel JP, Mackenzie J, Murray K, Will RG. Collins SJ, et al. Among authors: poleggi a. Brain. 2006 Sep;129(Pt 9):2278-87. doi: 10.1093/brain/awl159. Epub 2006 Jul 1. Brain. 2006. PMID: 16816392 Free article.
Codon 129 polymorphism of prion protein gene in sporadic Alzheimer's disease.
Poleggi A, Bizzarro A, Acciarri A, Antuono P, Bagnoli S, Cellini E, Forno GD, Giannattasio C, Lauria A, Matera MG, Nacmias B, Puopolo M, Seripa D, Sorbi S, Wekstein DR, Pocchiari M, Masullo C. Poleggi A, et al. Eur J Neurol. 2008 Feb;15(2):173-8. doi: 10.1111/j.1468-1331.2007.02021.x. Eur J Neurol. 2008. PMID: 18217885
Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele.
Giannattasio C, Poleggi A, Puopolo M, Pocchiari M, Antuono P, Dal Forno G, Wekstein DR, Matera MG, Seripa D, Acciarri A, Bizzarro A, Lauria A, Masullo C. Giannattasio C, et al. Among authors: poleggi a. Dement Geriatr Cogn Disord. 2008;25(4):354-8. doi: 10.1159/000119730. Epub 2008 Mar 7. Dement Geriatr Cogn Disord. 2008. PMID: 18332630
Genomic and post-genomic analyses of human prion diseases.
Pocchiari M, Poleggi A, Principe S, Graziano S, Cardone F. Pocchiari M, et al. Among authors: poleggi a. Genome Med. 2009 Jun 22;1(6):63. doi: 10.1186/gm63. Genome Med. 2009. PMID: 19566915 Free PMC article.
Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease.
Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, Heinemann U, Zerr I, Knight RS, Mitrova E, van Duijn C, Budka H. Kovacs GG, et al. Among authors: poleggi a. Alzheimer Dis Assoc Disord. 2010 Jan-Mar;24(1):104-7. doi: 10.1097/WAD.0b013e3181ad378c. Alzheimer Dis Assoc Disord. 2010. PMID: 19571726
44 results