Similar articles for PMID: 25279981

Year	Number of Results
1991	1
1993	2
1994	3
1995	3
1996	2
1998	2
1999	5
2000	4
2001	2
2002	1
2003	1
2004	3
2006	2
2007	3
2008	3
2009	8
2010	9
2011	8
2012	4
2013	8
2014	9
2015	7
2017	1
2018	3
2019	3
2020	1
2021	3
2022	6
2023	4
2024	0

1

Ascertainment bias causes false signal of anticipation in genetic prion disease.

Minikel EV, Zerr I, Collins SJ, Ponto C, Boyd A, Klug G, Karch A, Kenny J, Collinge J, Takada LT, Forner S, Fong JC, Mead S, Geschwind MD. Minikel EV, et al. Am J Hum Genet. 2014 Oct 2;95(4):371-82. doi: 10.1016/j.ajhg.2014.09.003. Am J Hum Genet. 2014. PMID: 25279981 Free PMC article.

2

Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.

Pocchiari M, Poleggi A, Puopolo M, D'Alessandro M, Tiple D, Ladogana A. Pocchiari M, et al. PLoS One. 2013;8(4):e60376. doi: 10.1371/journal.pone.0060376. Epub 2013 Apr 2. PLoS One. 2013. PMID: 23565236 Free PMC article.

3

Preliminary evidence for anticipation in genetic E200K Creutzfeldt-Jakob disease.

Rosenmann H, Kahana E, Korczyn AD, Kahana I, Chapman J, Gabizon R. Rosenmann H, et al. Neurology. 1999 Oct 12;53(6):1328-9. doi: 10.1212/wnl.53.6.1328. Neurology. 1999. PMID: 10522892

4

Pseudo-anticipation in Creutzfeldt-Jakob disease is due to a rhomboid-shaped artifact.

Cohen OS, Kahana E, Korczyn AD, Ziv-Baran T, Nitsan Z, Appel S, Rosenmann H, Chapman J. Cohen OS, et al. Eur J Neurol. 2020 Apr;27(4):596-602. doi: 10.1111/ene.14138. Epub 2020 Feb 3. Eur J Neurol. 2020. PMID: 31814268

5

Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype.

Ghoshal N, Cali I, Perrin RJ, Josephson SA, Sun N, Gambetti P, Morris JC. Ghoshal N, et al. Arch Neurol. 2009 Oct;66(10):1240-6. doi: 10.1001/archneurol.2009.224. Arch Neurol. 2009. PMID: 19822779 Free PMC article.

6

[Human prion diseases: the Hungarian experience].

Kovács GG, Bakos A, Mitrova E, Minárovits J, László L, Majtényi K. Kovács GG, et al. Ideggyogy Sz. 2007 Nov 30;60(11-12):447-52. Ideggyogy Sz. 2007. PMID: 18200749 Hungarian.

7

Biological network inferences for a protection mechanism against familial Creutzfeldt-Jakob disease with E200K pathogenic mutation.

Lee SM, Chung M, Hwang KJ, Ju YR, Hyeon JW, Park JS, Kim CK, Choi S, Lee J, Kim SY. Lee SM, et al. BMC Med Genomics. 2014 Aug 22;7:52. doi: 10.1186/1755-8794-7-52. BMC Med Genomics. 2014. PMID: 25149502 Free PMC article.

8

The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.

Bregman N, Shiner T, Kavé G, Alcalay R, Gana-Weisz M, Goldstein O, Glinka T, Aizenstein O, Bashat DB, Alcalay Y, Mirelman A, Thaler A, Giladi N, Omer N. Bregman N, et al. BMC Neurol. 2023 Apr 14;23(1):151. doi: 10.1186/s12883-023-03193-8. BMC Neurol. 2023. PMID: 37069531 Free PMC article.

9

Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature.

Mancuso M, Siciliano G, Capellari S, Orsucci D, Moretti P, Di Fede G, Suardi S, Strammiello R, Parchi P, Tagliavini F, Murri L. Mancuso M, et al. Neurol Sci. 2009 Oct;30(5):417-20. doi: 10.1007/s10072-009-0118-7. Epub 2009 Jul 14. Neurol Sci. 2009. PMID: 19597763

10

Iatrogenic and sporadic Creutzfeldt-Jakob disease in 2 sisters without mutation in the prion protein gene.

Frontzek K, Moos R, Schaper E, Jann L, Herfs G, Zimmermann DR, Aguzzi A, Budka H. Frontzek K, et al. Prion. 2015;9(6):444-8. doi: 10.1080/19336896.2015.1121356. Prion. 2015. PMID: 26634863 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

101 results

Results by year