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213 related items for PubMed ID: 15235800

  • 1. Oligodendrocytes within astrocytes ("emperipolesis") in the white matter in Creutzfeldt-Jakob disease.
    Shintaku M, Yutani C.
    Acta Neuropathol; 2004 Sep; 108(3):201-6. PubMed ID: 15235800
    [Abstract] [Full Text] [Related]

  • 2. Microglial and astrocytic change in brains of Creutzfeldt-Jakob disease: an immunocytochemical and quantitative study.
    Aoki T, Kobayashi K, Isaki K.
    Clin Neuropathol; 1999 Sep; 18(2):51-60. PubMed ID: 10192699
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  • 4. Modifications of oligodendroglial cells in spongiform encephalopathies.
    El Hachimi KH, Chaunu MP, Brown P, Foncin JF.
    Exp Neurol; 1998 Nov; 154(1):23-30. PubMed ID: 9875264
    [Abstract] [Full Text] [Related]

  • 5. Oligodendrocytes within astrocytes ("emperipolesis") in the cerebral white matter in hepatic and hypoglycemic encephalopathy.
    Nishie M, Mori F, Houzen H, Yamaguchi J, Jensen PH, Wakabayashi K.
    Neuropathology; 2006 Feb; 26(1):62-5. PubMed ID: 16521481
    [Abstract] [Full Text] [Related]

  • 6. White matter lesions in Creutzfeldt-Jakob disease. A short review.
    Masullo C, Macchi G, Pocchiari M.
    Ital J Neurol Sci; 1992 Dec; 13(9 Suppl 14):27-30. PubMed ID: 1345738
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  • 7. Enhanced expression of 14-3-3 proteins in reactive astrocytes in Creutzfeldt-Jakob disease brains.
    Kawamoto Y, Akiguchi I, Jarius C, Budka H.
    Acta Neuropathol; 2004 Oct; 108(4):302-8. PubMed ID: 15235801
    [Abstract] [Full Text] [Related]

  • 8. Altered gene transcription linked to astrocytes and oligodendrocytes in frontal cortex in Creutzfeldt-Jakob disease.
    Andres Benito P, Dominguez Gonzalez M, Ferrer I.
    Prion; 2018 Oct; 12(3-4):216-225. PubMed ID: 30009661
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  • 9. Neuropathology of Creutzfeldt-Jakob disease in Japan. With special reference to the panencephalopathic type.
    Mizutani T.
    Acta Pathol Jpn; 1981 Nov; 31(6):903-22. PubMed ID: 7032195
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  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Familial presenile dementia with CJD-like lesions: preliminary results.
    Kosaka K, Arai H, Ikeda K.
    Clin Neuropathol; 1985 Oct; 4(4):149-55. PubMed ID: 2865022
    [Abstract] [Full Text] [Related]

  • 13. Familial Creutzfeldt-Jakob disease: three autopsy cases of the panencephalopathic type.
    Seno H, Ishino H, Inagaki T, Yamamori C, Iijima M, Tanaka S, Kobayashi S, Shimizu Y, Torii I, Harada T.
    Clin Neuropathol; 1994 Oct; 13(4):185-91. PubMed ID: 7955663
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  • 14. 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
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  • 15. [An autopsy case of panencephalopathic type of Creutzfeldt-Jakob disease: an early clinical sign documented by magnetic resonance imaging].
    Okiyama R, Tsuchiya K, Furukawa T, Tsukagoshi H, Kosaka K.
    Rinsho Shinkeigaku; 1989 Aug; 29(8):1048-51. PubMed ID: 2689033
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  • 16. [Panencephalopathy of the Creutzfeldt-Jakob disease type].
    Gertz HJ, Stoltenburg G, Cruz-Sanchez F, Lafuente J, Schopol R.
    Nervenarzt; 1988 Feb; 59(2):110-2. PubMed ID: 3283576
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  • 17. GluR2/3, NMDAepsilon1 and GABAA receptors in Creutzfeldt-Jakob disease.
    Ferrer I, Puig B.
    Acta Neuropathol; 2003 Oct; 106(4):311-8. PubMed ID: 12835949
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  • 18. [Atypical clinicoradiological course in a case panancephalic variant of Creutzfeldt-Jakob].
    Pascual Lozano A, Salvador-Aliaga A, Coret F, Lainez-Andres J.
    Neurologia; 2006 Oct; 21(8):439-43. PubMed ID: 17013790
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  • 19. 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
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  • 20. 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
    [Abstract] [Full Text] [Related]

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