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778 related items for PubMed ID: 18410280

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease.
    Saito Y, Iwasaki Y, Aiba I, Kitamoto T, Yoshida M, Hashizume Y.
    Neuropathology; 2011 Oct; 31(5):523-30. PubMed ID: 21175861
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset.
    Iwasaki Y, Mori K, Ito M, Mimuro M, Kitamoto T, Yoshida M.
    Neuropathology; 2017 Feb; 37(1):78-85. PubMed ID: 27436355
    [Abstract] [Full Text] [Related]

  • 6. MM2-thalamic-type sporadic Creutzfeldt-Jakob disease with widespread neocortical pathology.
    Hirose K, Iwasaki Y, Izumi M, Yoshida M, Hashizume Y, Kitamoto T, Sahashi K.
    Acta Neuropathol; 2006 Oct; 112(4):503-11. PubMed ID: 16957926
    [Abstract] [Full Text] [Related]

  • 7. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
    Hama T, Iwasaki Y, Niwa H, Yoshida M, Hashizume Y, Kitamoto T, Murakami N, Sobue G.
    Neuropathology; 2009 Dec; 29(6):727-34. PubMed ID: 19422533
    [Abstract] [Full Text] [Related]

  • 8. Clinical features and diagnosis of the MM2 cortical subtype of sporadic Creutzfeldt-Jakob disease.
    Krasnianski A, Meissner B, Schulz-Schaeffer W, Kallenberg K, Bartl M, Heinemann U, Varges D, Kretzschmar HA, Zerr I.
    Arch Neurol; 2006 Jun; 63(6):876-80. PubMed ID: 16769870
    [Abstract] [Full Text] [Related]

  • 9. An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type.
    Iwasaki Y, Mori K, Ito M, Nagaoka M, Ieda T, Kitamoto T, Yoshida M, Hashizume Y.
    Neuropathology; 2011 Oct; 31(5):540-8. PubMed ID: 21269331
    [Abstract] [Full Text] [Related]

  • 10. Sporadic Creutzfeldt-Jakob disease without dementia at onset: clinical features, laboratory tests and sequential diffusion MRI (in an autopsy-proven case).
    Pauri F, Amabile G, Fattapposta F, Pierallini A, Bianco F.
    Neurol Sci; 2004 Oct; 25(4):234-7. PubMed ID: 15549511
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.
    Iwasaki Y, Yokoi F, Tatsumi S, Mimuro M, Iwai K, Kitamoto T, Yoshida M.
    Neuropathology; 2013 Oct; 33(5):568-75. PubMed ID: 23320809
    [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 09; 72(23):1994-2001. PubMed ID: 19506221
    [Abstract] [Full Text] [Related]

  • 14. Sporadic Creutzfeldt-Jakob disease: clinical and diagnostic characteristics of the rare VV1 type.
    Meissner B, Westner IM, Kallenberg K, Krasnianski A, Bartl M, Varges D, Bösenberg C, Kretzschmar HA, Knauth M, Schulz-Schaeffer WJ, Zerr I.
    Neurology; 2005 Nov 22; 65(10):1544-50. PubMed ID: 16221949
    [Abstract] [Full Text] [Related]

  • 15. Neuropathologic characteristics of brainstem lesions in sporadic Creutzfeldt-Jakob disease.
    Iwasaki Y, Hashizume Y, Yoshida M, Kitamoto T, Sobue G.
    Acta Neuropathol; 2005 Jun 22; 109(6):557-66. PubMed ID: 15933870
    [Abstract] [Full Text] [Related]

  • 16. Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology.
    Iwasaki Y, Tatsumi S, Mimuro M, Kitamoto T, Hashizume Y, Yoshida M.
    J Neurol Sci; 2014 Jun 15; 341(1-2):97-104. PubMed ID: 24787503
    [Abstract] [Full Text] [Related]

  • 17. Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration.
    Hayashi Y, Iwasaki Y, Waza M, Shibata H, Akagi A, Kimura A, Inuzuka T, Satoh K, Kitamoto T, Yoshida M, Shimohata T.
    Prion; 2019 Jan 15; 13(1):124-131. PubMed ID: 31219399
    [Abstract] [Full Text] [Related]

  • 18. An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.
    Iwasaki Y, Saito Y, Aiba I, Kobayashi A, Mimuro M, Kitamoto T, Yoshida M.
    Neuropathology; 2017 Jun 15; 37(3):241-248. PubMed ID: 28568896
    [Abstract] [Full Text] [Related]

  • 19. Decreased regional cerebral blood flow in the bilateral thalami and medulla oblongata determined by an easy Z-score (eZIS) analysis of (99m)Tc-ECD-SPECT images in a case of MM2-thalamic-type sporadic Creutzfeldt-Jakob disease.
    Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Hatano T, Tatsumi S, Satoh K, Kimura A, Kitamoto T, Yoshida M, Inuzuka T.
    J Neurol Sci; 2015 Nov 15; 358(1-2):447-52. PubMed ID: 26421831
    [Abstract] [Full Text] [Related]

  • 20. Creutzfeldt-Jakob disease.
    Iwasaki Y.
    Neuropathology; 2017 Apr 15; 37(2):174-188. PubMed ID: 28028861
    [Abstract] [Full Text] [Related]

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