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Volumn 8, Issue 3, 1998, Pages 567-570

FFI cases from the United States, Australia, and Japan

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; AUSTRALIA; BRAIN; CASE REPORT; FATALITY; FEMALE; GENETICS; HUMAN; JAPAN; MALE; MIDDLE AGED; PATHOLOGY; PRION; PRION DISEASE; UNITED STATES;

EID: 0032112988     PISSN: 10156305     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1750-3639.1998.tb00184.x     Document Type: Article
Times cited : (6)

References (16)
  • 1
    • 0026801958 scopus 로고
    • APrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease
    • Bosque PJ, Vnencak-Jones CL, Johnson MD, Whitlock JA, Mclean MJ (1992) APrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease. Neurology 42:1864-1870
    • (1992) Neurology , vol.42 , pp. 1864-1870
    • Bosque, P.J.1    Vnencak-Jones, C.L.2    Johnson, M.D.3    Whitlock, J.A.4    Mclean, M.J.5
  • 5
    • 0028835989 scopus 로고
    • Fatal familial insomnia and familial CreutzfeldtJakob disease: Clinical, pathological and molecular features
    • Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E (1995) Fatal familial insomnia and familial CreutzfeldtJakob disease: clinical, pathological and molecular features. Brain Pathol 5: 43-51
    • (1995) Brain Pathol , vol.5 , pp. 43-51
    • Gambetti, P.1    Parchi, P.2    Petersen, R.B.3    Chen, S.G.4    Lugaresi, E.5
  • 9
    • 0019801464 scopus 로고
    • The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer disease
    • Masters CL, Gajdusek DC, Gibbs, CJ (1981 ) The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer disease. Brain 104: 535-558
    • (1981) Brain , vol.104 , pp. 535-558
    • Masters, C.L.1    Gajdusek, D.C.2    Gibbs, C.J.3
  • 10
    • 0030821246 scopus 로고    scopus 로고
    • The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathological phenotypes in an Australian kindred
    • McLean CA, Storey E, Gardner RJM, Tannenberg AEG, Cervenakova L, Brown P (1997) The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathological phenotypes in an Australian kindred. Neurology, 49: 552-558
    • (1997) Neurology , vol.49 , pp. 552-558
    • McLean, C.A.1    Storey, E.2    Rjm, G.3    Aeg, T.4    Cervenakova, L.5    Brown, P.6
  • 11
    • 0029961971 scopus 로고    scopus 로고
    • Fatal familial insomnia with a mutation at codon 178 of the prion protein gene: First report from Japan
    • Nagayama M, Shinohara Y, Furukawa H, Kitamoto T (1996) Fatal familial insomnia with a mutation at codon 178 of the prion protein gene : first report from Japan. Neurology 47: 1313-1316
    • (1996) Neurology , vol.47 , pp. 1313-1316
    • Nagayama, M.1    Shinohara, Y.2    Furukawa, H.3    Kitamoto, T.4
  • 14
    • 0031436335 scopus 로고    scopus 로고
    • The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells
    • Rieger R, Ednhofer F, Lasmézas Cl, Weiss S (1997) The human 37-kDa laminin receptor precursor interacts with the prion protein in eukaryotic cells. Nat Med 3: 13831388
    • (1997) Nat Med , vol.3 , pp. 13831388
    • Rieger, R.1    Ednhofer, F.2    Cl, L.3    Weiss, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.