169 related articles for article (PubMed ID: 10811709)
1. Trends in mortality from sporadic Creutzfeldt-Jakob disease in France 1992-7.
d'Aignaux JH; Laplanche JL; Delasnerie-Lauprêtre N; Brandel JP; Peoc'h K; Salomon D; Hauw JJ; Alpérovitch A
J Neurol Neurosurg Psychiatry; 2000 Jun; 68(6):787-9. PubMed ID: 10811709
[TBL] [Abstract][Full Text] [Related]
2. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease.
Alperovitch A; Zerr I; Pocchiari M; Mitrova E; de Pedro Cuesta J; Hegyi I; Collins S; Kretzschmar H; van Duijn C; Will RG
Lancet; 1999 May; 353(9165):1673-4. PubMed ID: 10335789
[No Abstract] [Full Text] [Related]
3. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
Parchi P; Castellani R; Capellari S; Ghetti B; Young K; Chen SG; Farlow M; Dickson DW; Sima AA; Trojanowski JQ; Petersen RB; Gambetti P
Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
[TBL] [Abstract][Full Text] [Related]
4. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
Mitrová E; Belay G
Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
[TBL] [Abstract][Full Text] [Related]
5. Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.
Hauw JJ; Sazdovitch V; Laplanche JL; Peoc'h K; Kopp N; Kemeny J; Privat N; Delasnerie-Lauprêtre N; Brandel JP; Deslys JP; Dormont D; Alpérovitch A
Neurology; 2000 Apr; 54(8):1641-6. PubMed ID: 10762506
[TBL] [Abstract][Full Text] [Related]
6. Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.
Bougard D; Bélondrade M; Mayran C; Bruyère-Ostells L; Lehmann S; Fournier-Wirth C; Knight RS; Will RG; Green AJE
Emerg Infect Dis; 2018 Jul; 24(7):1364-1366. PubMed ID: 29912702
[TBL] [Abstract][Full Text] [Related]
7. [Epidemiological surveillance of Creutzfeldt-Jakob in France].
Brandel JP; Salomon D; Capek I; Vaillant V; Alpérovitch A
Rev Neurol (Paris); 2009; 165(8-9):684-93. PubMed ID: 19467685
[TBL] [Abstract][Full Text] [Related]
8. Prospective 10-year surveillance of human prion diseases in Japan.
Nozaki I; Hamaguchi T; Sanjo N; Noguchi-Shinohara M; Sakai K; Nakamura Y; Sato T; Kitamoto T; Mizusawa H; Moriwaka F; Shiga Y; Kuroiwa Y; Nishizawa M; Kuzuhara S; Inuzuka T; Takeda M; Kuroda S; Abe K; Murai H; Murayama S; Tateishi J; Takumi I; Shirabe S; Harada M; Sadakane A; Yamada M
Brain; 2010 Oct; 133(10):3043-57. PubMed ID: 20855418
[TBL] [Abstract][Full Text] [Related]
9. Differences of apparent diffusion coefficient values in patients with Creutzfeldt-Jakob disease according to the codon 129 genotype.
Galanaud D; Dormont D; Haïk S; Chiras J; Brandel JP; Ranjeva JP
AJNR Am J Neuroradiol; 2008 Aug; 29(7):E57; author reply E58. PubMed ID: 18372408
[No Abstract] [Full Text] [Related]
10. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
Hainfellner JA; Parchi P; Kitamoto T; Jarius C; Gambetti P; Budka H
Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778
[TBL] [Abstract][Full Text] [Related]
11. Sporadic Creutzfeldt-Jakob disease in the United Kingdom: analysis of epidemiological surveillance data for 1970-96.
Cousens SN; Zeidler M; Esmonde TF; De Silva R; Wilesmith JW; Smith PG; Will RG
BMJ; 1997 Aug; 315(7105):389-95. PubMed ID: 9277601
[TBL] [Abstract][Full Text] [Related]
12. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I
Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565
[TBL] [Abstract][Full Text] [Related]
13. Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.
Diack AB; Boyle A; Plinston C; Hunt E; Bishop MT; Will RG; Manson JC
Brain; 2019 May; 142(5):1416-1428. PubMed ID: 30938429
[TBL] [Abstract][Full Text] [Related]
14. [Human prion diseases: the Hungarian experience].
Kovács GG; Bakos A; Mitrova E; Minárovits J; László L; Majtényi K
Ideggyogy Sz; 2007 Nov; 60(11-12):447-52. PubMed ID: 18200749
[TBL] [Abstract][Full Text] [Related]
15. Prion Strain Characterization of a Novel Subtype of Creutzfeldt-Jakob Disease.
Galeno R; Di Bari MA; Nonno R; Cardone F; Sbriccoli M; Graziano S; Ingrosso L; Fiorini M; Valanzano A; Pasini G; Poleggi A; Vinci R; Ladogana A; Puopolo M; Monaco S; Agrimi U; Zanusso G; Pocchiari M
J Virol; 2017 Jun; 91(11):. PubMed ID: 28298604
[TBL] [Abstract][Full Text] [Related]
16. Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2.
Samman I; Schulz-Schaeffer WJ; Wöhrle JC; Sommer A; Kretzschmar HA; Hennerici M
J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):678-81. PubMed ID: 10519881
[TBL] [Abstract][Full Text] [Related]
17. Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype.
Yeo MJ; Lee SH; Lee SY; Jeon YC; Park SJ; Cho HJ; Choi KC; Kim YS; Kim SH
J Clin Neurosci; 2013 Jan; 20(1):180-2. PubMed ID: 22999564
[TBL] [Abstract][Full Text] [Related]
18. Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?
Kobayashi A; Parchi P; Yamada M; Brown P; Saverioni D; Matsuura Y; Takeuchi A; Mohri S; Kitamoto T
J Virol; 2015 Apr; 89(7):3939-46. PubMed ID: 25609817
[TBL] [Abstract][Full Text] [Related]
19. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease.
Worrall BB; Herman ST; Capellari S; Lynch T; Chin S; Gambetti P; Parchi P
J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):671-4. PubMed ID: 10519879
[TBL] [Abstract][Full Text] [Related]
20. 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
Brain; 2006 Sep; 129(Pt 9):2278-87. PubMed ID: 16816392
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
