536 related articles for article (PubMed ID: 16354106)
1. Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.
Schoch G; Seeger H; Bogousslavsky J; Tolnay M; Janzer RC; Aguzzi A; Glatzel M
PLoS Med; 2006 Feb; 3(2):e14. PubMed ID: 16354106
[TBL] [Abstract][Full Text] [Related]
2. Intracerebral distribution of the abnormal isoform of the prion protein in sporadic Creutzfeldt-Jakob disease and fatal insomnia.
Parchi P; Capellari S; Gambetti P
Microsc Res Tech; 2000 Jul; 50(1):16-25. PubMed ID: 10871544
[TBL] [Abstract][Full Text] [Related]
3. [Sporadic Creutzfeldt-Jakob disease: phenotypic variability].
Moreno MJ; Romero J
Neurologia; 2002; 17(7):366-77. PubMed ID: 12236956
[TBL] [Abstract][Full Text] [Related]
4. Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.
Glatzel M; Abela E; Maissen M; Aguzzi A
N Engl J Med; 2003 Nov; 349(19):1812-20. PubMed ID: 14602879
[TBL] [Abstract][Full Text] [Related]
5. Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles.
Lewis V; Hill AF; Klug GM; Boyd A; Masters CL; Collins SJ
Neurology; 2005 Jul; 65(1):113-8. PubMed ID: 16009895
[TBL] [Abstract][Full Text] [Related]
6. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
[TBL] [Abstract][Full Text] [Related]
7. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Righetti PG; Ferrari S; Terrin L; Farinazzo A; Cardone F; Pocchiari M; Rizzuto N; Monaco S
Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
[TBL] [Abstract][Full Text] [Related]
8. Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Ferrari S; Cardone F; Zampieri P; Gelati M; Fiorini M; Farinazzo A; Gardiman M; Cavallaro T; Bentivoglio M; Righetti PG; Pocchiari M; Rizzuto N; Monaco S
N Engl J Med; 2003 Feb; 348(8):711-9. PubMed ID: 12594315
[TBL] [Abstract][Full Text] [Related]
9. Classification of sporadic Creutzfeldt-Jakob disease revisited.
Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
[TBL] [Abstract][Full Text] [Related]
10. Polymorphism at codon 129 of the prion protein gene determines cerebellar pathology in Creutzfeldt-Jakob disease.
Schulz-Schaeffer WJ; Giese A; Windl O; Kretzschmar HA
Clin Neuropathol; 1996; 15(6):353-7. PubMed ID: 8937783
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease.
Favereaux A; Quadrio I; Vital C; Perret-Liaudet A; Anne O; Laplanche JL; Petry KG; Vital A
Arch Neurol; 2004 May; 61(5):747-50. PubMed ID: 15148153
[TBL] [Abstract][Full Text] [Related]
13. MRI lesion profiles in sporadic Creutzfeldt-Jakob disease.
Meissner B; Kallenberg K; Sanchez-Juan P; Collie D; Summers DM; Almonti S; Collins SJ; Smith P; Cras P; Jansen GH; Brandel JP; Coulthart MB; Roberts H; Van Everbroeck B; Galanaud D; Mellina V; Will RG; Zerr I
Neurology; 2009 Jun; 72(23):1994-2001. PubMed ID: 19506221
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Molecular diagnostic tools in Creutzfeldt-Jakob disease and other prion disorders.
Van Everbroeck B; Boons J; De Leenheir E; Lübke U; Cras P
Expert Rev Mol Diagn; 2004 May; 4(3):351-9. PubMed ID: 15137902
[TBL] [Abstract][Full Text] [Related]
16. Molecular typing of PrPres in human sporadic CJD brain tissue.
Lewis V; Klug GM; Hill AF; Collins SJ
Methods Mol Biol; 2008; 459():241-7. PubMed ID: 18576159
[TBL] [Abstract][Full Text] [Related]
17. [The mystery of prion proteins: from neurodegenerative diseases to the biology of reproduction].
Peoc'h K
Ann Biol Clin (Paris); 2005; 63(2):121-6. PubMed ID: 15771969
[TBL] [Abstract][Full Text] [Related]
18. Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Ferrari S; Benedetti D; Sbriccoli M; Rizzuto N; Monaco S
Ann N Y Acad Sci; 2009 Jul; 1170():637-43. PubMed ID: 19686205
[TBL] [Abstract][Full Text] [Related]
19. Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle.
Kovacs GG; Lindeck-Pozza E; Chimelli L; Araújo AQ; Gabbai AA; Ströbel T; Glatzel M; Aguzzi A; Budka H
Ann Neurol; 2004 Jan; 55(1):121-5. PubMed ID: 14705121
[TBL] [Abstract][Full Text] [Related]
20. Codon 129 polymorphism specific cerebrospinal fluid proteome pattern in sporadic Creutzfeldt-Jakob disease and the implication of glycolytic enzymes in prion-induced pathology.
Gawinecka J; Dieks J; Asif AR; Carimalo J; Heinemann U; Streich JH; Dihazi H; Schulz-Schaeffer W; Zerr I
J Proteome Res; 2010 Nov; 9(11):5646-57. PubMed ID: 20866111
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
