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Journal Abstract Search

174 related items for PubMed ID: 9366185

  • 1. [Multiple solitary lesions in deep white matter in the early stage of Creutzfeldt-Jakob disease. A case report].
    Nomoto K, Murahashi M, Jimi T, Wakayama Y.
    Rinsho Shinkeigaku; 1997 Jun; 37(6):528-31. PubMed ID: 9366185
    [Abstract] [Full Text] [Related]

  • 2. [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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  • 3. [A case of Creutzfeldt-Jakob disease (CJD) started with monoparesis of the left arm].
    Obi T, Takatsu M, Kitamoto T, Mizoguchi K, Nishimura Y.
    Rinsho Shinkeigaku; 1996 Nov; 36(11):1245-8. PubMed ID: 9046857
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  • 4. [Juvenile onset Creutzfeldt-Jakob disease with the history of neurosurgical operation].
    Sato M, Murahashi M, Hara H, Jimi T, Wakayama Y.
    Rinsho Shinkeigaku; 2000 May; 40(5):428-32. PubMed ID: 11002723
    [Abstract] [Full Text] [Related]

  • 5. [A case of clinically diagnosed Creutzfeldt-Jakob disease with serial MRI diffusion weighted images].
    Hirose Y, Mokuno K, Abe Y, Sobue G, Matsukawa N.
    Rinsho Shinkeigaku; 1998 Aug; 38(8):779-82. PubMed ID: 9916529
    [Abstract] [Full Text] [Related]

  • 6. [Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].
    Iwaski Y, Sone M, Kato T, Yoshida E, Indo T, Yoshida M, Hashizume Y, Yamada M.
    Rinsho Shinkeigaku; 1999 Aug; 39(8):800-6. PubMed ID: 10586622
    [Abstract] [Full Text] [Related]

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

  • 8. [Creutzfeldt-Jakob disease associated with ocular dipping--a case report].
    Haraguchi T, Akaura K, Yabuki S.
    Rinsho Shinkeigaku; 1998 Jan; 38(1):70-3. PubMed ID: 9597917
    [Abstract] [Full Text] [Related]

  • 9. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis].
    Imaiso Y, Mitsuo K.
    Rinsho Shinkeigaku; 1998 Jan; 38(10-11):920-5. PubMed ID: 10203975
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  • 12. [Reversible white matter lesions and antithyroid antibodies in the cerebrospinal fluid in Hashimoto's encephalopathy: a case report].
    Wakai M, Nishikage H, Goshima K.
    Rinsho Shinkeigaku; 2004 Jul; 44(7):432-7. PubMed ID: 15384704
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  • 14. [An autopsy case of ataxic form of Creutzfeldt-Jakob disease].
    Seno H, Ishino H, Inagaki T, Yamamori C, Iijima M, Tanaka S, Ideshita H, Yoshinaga J, Hikiji A.
    No To Shinkei; 1992 Feb; 44(2):177-81. PubMed ID: 1567739
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  • 16. [Case report of a patient with Hashimoto's encephalopathy associated with Basedow's disease mimicking Creutzfeldt-Jakob disease].
    Sakurai T, Tanaka Y, Koumura A, Hayashi Y, Kimura A, Hozumi I, Yoneda M, Inuzuka T.
    Brain Nerve; 2008 May; 60(5):559-65. PubMed ID: 18516979
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  • 18. Early clinical and laboratory diagnosis of Creutzfeldt-Jakob disease.
    Felgenhauer K, Weber T, Poser S.
    Dev Biol Stand; 1993 May; 80():125-30. PubMed ID: 8270102
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