These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


183 related items for PubMed ID: 2865022

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

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Features of Creutzfeldt-Jakob disease in brains of patients with familial dementia of Alzheimer type.
    Ball MJ.
    Can J Neurol Sci; 1980 Feb; 7(1):51-7. PubMed ID: 6992964
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. [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
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [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
    [Abstract] [Full Text] [Related]

  • 8. [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]

  • 9. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
    Dervaux A, Vicart S, Lopes F, Le Borgne MH.
    Encephale; 2001 Jun; 27(2):194-7. PubMed ID: 11407273
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. [Familial presenile dementia: Gerstmann-Sträussler-Scheinker's syndrome (author's transl)].
    Warter JM, Steinmetz G, Heldt N, Rumbach L, Marescaux C, Eber AM, Collard M, Rohmer F, Floquet J, Guedenet JC, Gehin P, Weber M.
    Rev Neurol (Paris); 1982 Nov; 138(2):107-21. PubMed ID: 7048484
    [Abstract] [Full Text] [Related]

  • 12. Panencephalopathic type of Creutzfeldt-Jakob disease with neuropathologic features similar to Pick's disease.
    Pietrini V, Danieli D, Bevilacqua P, Lechi A.
    Clin Neuropathol; 1993 Nov; 12(1):1-6. PubMed ID: 7679958
    [Abstract] [Full Text] [Related]

  • 13. A case of Creutzfeldt-Jakob disease.
    Rodda RA.
    Clin Exp Neurol; 1977 Nov; 14():108-16. PubMed ID: 358185
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [A clinicopathological case of progressive aphasia].
    Deruaz JP, Assal G, Peter-Favre C.
    Rev Neurol (Paris); 1993 Sep; 149(3):186-91. PubMed ID: 8235210
    [Abstract] [Full Text] [Related]

  • 16. [An autopsy case of corticobasal degeneration clinically misdiagnosed as Pick's disease].
    Oda T, Ikeda K, Akamatsu W, Iwabuchi K, Akiyama H, Kondo H, Seta K, Kato Y, Kogure T, Hori K.
    Seishin Shinkeigaku Zasshi; 1995 Sep; 97(9):757-69. PubMed ID: 8552729
    [Abstract] [Full Text] [Related]

  • 17. [A case of familial juvenile Alzheimer's disease with apallic state at the relatively early stage and various neurological features--a clinicopathological study].
    Fukutani Y, Nakamura I, Kobayashi K, Yamaguchi N, Matsubara R, Kiyota Y.
    Rinsho Shinkeigaku; 1989 May; 29(5):633-8. PubMed ID: 2791415
    [Abstract] [Full Text] [Related]

  • 18. [An autopsied case of atypical presenile dementia which shows lobar atrophy, severe neurofibrillary tangles and calcification].
    Ujihira N, Hashizume Y, Takagi T, Ito M.
    Rinsho Shinkeigaku; 1997 Apr; 37(4):292-9. PubMed ID: 9248337
    [Abstract] [Full Text] [Related]

  • 19. [Hereditary dentatorubropallidoluysian atrophy--clinical variants in a family and degeneration of cerebral white matter in a proband].
    Miyashita K, Inuzuka T, Ishikawa A, Kondo H, Kawakami A, Takeda S, Ikuta F, Yuasa T.
    No To Shinkei; 1992 Mar; 44(3):279-84. PubMed ID: 1591106
    [Abstract] [Full Text] [Related]

  • 20. 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]


    Page: [Next] [New Search]
    of 10.