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351 related items for PubMed ID: 21450052

  • 1. 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
    [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
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  • 3. Neuropathologic characteristics of spinal cord lesions in sporadic Creutzfeldt-Jakob disease.
    Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G.
    Acta Neuropathol; 2005 Nov; 110(5):490-500. PubMed ID: 16175355
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  • 4. A traceback phenomenon can reveal the origin of prion infection.
    Kobayashi A, Asano M, Mohri S, Kitamoto T.
    Neuropathology; 2009 Oct; 29(5):619-24. PubMed ID: 19659941
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  • 5. 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 09; 72(23):1994-2001. PubMed ID: 19506221
    [Abstract] [Full Text] [Related]

  • 6. 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 09; 129(Pt 9):2266-77. PubMed ID: 16923954
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  • 7. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease.
    Iwasaki Y, Hashizume Y, Yoshida M, Kitamoto T, Sobue G.
    Acta Neuropathol; 2005 Jun 09; 109(6):557-66. PubMed ID: 15933870
    [Abstract] [Full Text] [Related]

  • 8. Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease.
    Debatin L, Streffer J, Geissen M, Matschke J, Aguzzi A, Glatzel M.
    Neurodegener Dis; 2008 Jun 09; 5(6):347-54. PubMed ID: 18349519
    [Abstract] [Full Text] [Related]

  • 9. 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 09; 3(2):e14. PubMed ID: 16354106
    [Abstract] [Full Text] [Related]

  • 10. 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 09; 1170():637-43. PubMed ID: 19686205
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  • 14. Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.
    Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P.
    Acta Neuropathol; 2021 Oct 09; 142(4):707-728. PubMed ID: 34324063
    [Abstract] [Full Text] [Related]

  • 15. Spatial correlations between the vacuolation, prion protein (PrPsc) deposits and the cerebral blood vessels in sporadic Creutzfeldt-Jakob disease.
    Armstrong RA.
    Curr Neurovasc Res; 2009 Nov 09; 6(4):239-45. PubMed ID: 19807656
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  • 16. Involvement of Dab1 in APP processing and beta-amyloid deposition in sporadic Creutzfeldt-Jakob patients.
    Gavín R, Ferrer I, del Río JA.
    Neurobiol Dis; 2010 Feb 09; 37(2):324-9. PubMed ID: 19853035
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  • 17. 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 Feb 09; 97(4):715-26. PubMed ID: 10842016
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  • 18. Prions from Sporadic Creutzfeldt-Jakob Disease Patients Propagate as Strain Mixtures.
    Cassard H, Huor A, Espinosa JC, Douet JY, Lugan S, Aron N, Vilette D, Delisle MB, Marín-Moreno A, Peran P, Beringue V, Torres JM, Ironside JW, Andreoletti O.
    mBio; 2020 Jun 16; 11(3):. PubMed ID: 32546613
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  • 19. [Morphological changes and prion accumulation in the cerebellar cortex in Creutzfeldt-Jacob disease].
    Karmysheva VIa, Gulevskaia TS, Pogodina VV.
    Arkh Patol; 2007 Jun 16; 69(6):10-5. PubMed ID: 18290372
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