BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

67 related articles for article (PubMed ID: 19519645)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. [Prionic neuroinvasion and cerebellar lesion in Creutzfeldt-Jakob disease].
    Karmysheva VIa; Pogodina VV
    Arkh Patol; 2006; 68(4):27-32. PubMed ID: 16986493
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A special report I. Prion protein (Prp)--amyloid plaques in the transmissible spongiform encephalopathies (TSEs) or prion disease revisited.
    Liberski PP; Bratosiewicz J; Waliś A; Kordek R; Jeffrey M; Brown P
    Pol J Pathol; 2001; 52(4):169-86. PubMed ID: 11915178
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. [Prion diseases, update].
    Kitamoto T
    Rinsho Shinkeigaku; 2001 Dec; 41(12):1223-5. PubMed ID: 12235843
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease.
    Kitamoto T; Tateishi J; Sato Y
    Ann Neurol; 1988 Oct; 24(4):537-42. PubMed ID: 3071243
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Immunohistochemical studies of the PrP(CJD) deposition in Creutzfeldt-Jakob disease.
    Tanaka S; Saito M; Morimatsu M; Ohama E
    Neuropathology; 2000 Jun; 20(2):124-33. PubMed ID: 10935449
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene.
    Skworc KH; Windl O; Schulz-Schaeffer WJ; Giese A; Bergk J; Nagele A; Vieregge P; Zerr I; Poser S; Kretzschmar HA
    Ann Neurol; 1999 Nov; 46(5):693-700. PubMed ID: 10553985
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: clinicopathological study of four autopsy cases.
    Ota S; Tsuchiya K; Anno M; Niizato K; Akiyama H
    Neuropathology; 2008 Feb; 28(1):43-50. PubMed ID: 18181834
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease.
    Iwasaki Y; Mimuro M; Yoshida M; Hashizume Y; Kitamoto T; Sobue G
    Neuropathology; 2008 Feb; 28(1):51-61. PubMed ID: 18181835
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. MM2-cortical-type sporadic Creutzfeldt-Jakob disease with early stage cerebral cortical pathology presenting with a rapidly progressive clinical course.
    Niimi Y; Iwasaki Y; Umemura T; Tanaka F; Yoshida M; Hashizume Y; Kitamoto T; Hirayama M; Sobue G
    Neuropathology; 2008 Dec; 28(6):645-51. PubMed ID: 18410280
    [TBL] [Abstract][Full Text] [Related]  

  • 19. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
    Hoshino A; Iwasaki Y; Izumi M; Kimura S; Ibi T; Kitamoto T; Yoshida M; Hashizume Y; Sahashi K
    Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.