383 related articles for article (PubMed ID: 19606064)
1. Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob disease.
Faucheux BA; Privat N; Brandel JP; Sazdovitch V; Laplanche JL; Maurage CA; Hauw JJ; Haïk S
J Neuropathol Exp Neurol; 2009 Aug; 68(8):892-901. PubMed ID: 19606064
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease.
Jarius C; Kovacs GG; Belay G; Hainfellner JA; Mitrova E; Budka H
Acta Neuropathol; 2003 May; 105(5):449-54. PubMed ID: 12677444
[TBL] [Abstract][Full Text] [Related]
4. [Morphological changes and prion accumulation in the cerebellar cortex in Creutzfeldt-Jacob disease].
Karmysheva VIa; Gulevskaia TS; Pogodina VV
Arkh Patol; 2007; 69(6):10-5. PubMed ID: 18290372
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Clusterin solubility and aggregation in Creutzfeldt-Jakob disease.
Freixes M; Puig B; Rodríguez A; Torrejón-Escribano B; Blanco R; Ferrer I
Acta Neuropathol; 2004 Oct; 108(4):295-301. PubMed ID: 15235804
[TBL] [Abstract][Full Text] [Related]
7. Prion protein deposition and abnormal synaptic protein expression in the cerebellum in Creutzfeldt-Jakob disease.
Ferrer I; Puig B; Blanco R; Martí E
Neuroscience; 2000; 97(4):715-26. PubMed ID: 10842016
[TBL] [Abstract][Full Text] [Related]
8. Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
Shimizu H; Yamada M; Matsubara N; Takano H; Umeda Y; Kawase Y; Kitamoto T; Nishizawa M; Takahashi H
Neuropathology; 2009 Dec; 29(6):735-43. PubMed ID: 19422537
[TBL] [Abstract][Full Text] [Related]
9. Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.
Kitamoto T; Shin RW; Doh-ura K; Tomokane N; Miyazono M; Muramoto T; Tateishi J
Am J Pathol; 1992 Jun; 140(6):1285-94. PubMed ID: 1351366
[TBL] [Abstract][Full Text] [Related]
10. Neuronal phosphorylated RNA-dependent protein kinase in Creutzfeldt-Jakob disease.
Paquet C; Bose A; Polivka M; Peoc'h K; Brouland JP; Keohane C; Hugon J; Gray F
J Neuropathol Exp Neurol; 2009 Feb; 68(2):190-8. PubMed ID: 19151623
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Neuropathological study of cerebellar degeneration in prion disease.
Yang Q; Hashizume Y; Yoshida M; Wang Y
Neuropathology; 1999 Jan; 19(1):33-9. PubMed ID: 19519645
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Selective PrP-like protein, doppel immunoreactivity in dystrophic neurites of senile plaques in Alzheimer's disease.
Ferrer I; Freixas M; Blanco R; Carmona M; Puig B
Neuropathol Appl Neurobiol; 2004 Aug; 30(4):329-37. PubMed ID: 15305978
[TBL] [Abstract][Full Text] [Related]
15. Tetracycline affects abnormal properties of synthetic PrP peptides and PrP(Sc) in vitro.
Tagliavini F; Forloni G; Colombo L; Rossi G; Girola L; Canciani B; Angeretti N; Giampaolo L; Peressini E; Awan T; De Gioia L; Ragg E; Bugiani O; Salmona M
J Mol Biol; 2000 Jul; 300(5):1309-22. PubMed ID: 10903871
[TBL] [Abstract][Full Text] [Related]
16. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
Di Fede G; Giaccone G; Limido L; Mangieri M; Suardi S; Puoti G; Morbin M; Mazzoleni G; Ghetti B; Tagliavini F
J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
[TBL] [Abstract][Full Text] [Related]
17. Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients.
Kobayashi A; Arima K; Ogawa M; Murata M; Fukuda T; Kitamoto T
Acta Neuropathol; 2008 Nov; 116(5):561-6. PubMed ID: 18751990
[TBL] [Abstract][Full Text] [Related]
18. Alpha-synuclein-immunoreactive deposits in human and animal prion diseases.
Haïk S; Privat N; Adjou KT; Sazdovitch V; Dormont D; Duyckaerts C; Hauw JJ
Acta Neuropathol; 2002 May; 103(5):516-20. PubMed ID: 11935269
[TBL] [Abstract][Full Text] [Related]
19. An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.
Yoshida H; Terada S; Ishizu H; Ikeda K; Hayabara T; Ikeda K; Deguchi K; Touge T; Kitamoto T; Kuroda S
Neuropathology; 2010 Apr; 30(2):159-64. PubMed ID: 19703264
[TBL] [Abstract][Full Text] [Related]
20. Prion protein oligomers in Creutzfeldt-Jakob disease detected by gel-filtration centrifuge columns.
Minaki H; Sasaki K; Honda H; Iwaki T
Neuropathology; 2009 Oct; 29(5):536-42. PubMed ID: 19389076
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
