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Volumn 8, Issue 3, 1998, Pages 559-561

The german FFI cases

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; BRAIN; FEMALE; GENETICS; GERMANY; HUMAN; MALE; MIDDLE AGED; PATHOLOGY; PRION; PRION DISEASE;

EID: 0032112577     PISSN: 10156305     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1750-3639.1998.tb00181.x     Document Type: Article
Times cited : (15)

References (12)
  • 1
    • 0026801958 scopus 로고
    • A PrP 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) A PrP 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
  • 3
    • 0028894604 scopus 로고
    • Codon 178 mutation of the human prion protein gene in a German family (Backer family): Sequencing data from 72 year-old celloidin-embedded brain tissue
    • Kretzschmar HA, Neumann M, Stavrou D. (1995) Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72 year-old celloidin-embedded brain tissue. Acta Neuropathol 89: 96-98
    • (1995) Acta Neuropathol , vol.89 , pp. 96-98
    • Kretzschmar, H.A.1    Neumann, M.2    Stavrou, D.3
  • 6
    • 0000940311 scopus 로고
    • Klinische und genealogische Beobachtungen bei einem Fall von spastischer Pseudosklerose
    • Meggendorfer F. (1930) Klinische und genealogische Beobachtungen bei einem Fall von spastischer Pseudosklerose. Zeitschrift für die gesamte Neurologie und Psychiatrie 128: 337-341
    • (1930) Zeitschrift für Die Gesamte Neurologie und Psychiatrie , vol.128 , pp. 337-341
    • Meggendorfer, F.1
  • 8
    • 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
  • 10
    • 0024595101 scopus 로고
    • Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorriisms
    • Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T. (1989) Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorriisms. Proc NatlAcad Sci USA 86: 2766-2770
    • (1989) Proc NatlAcad Sci USA , vol.86 , pp. 2766-2770
    • Orita, M.1    Iwahana, H.2    Kanazawa, H.3    Hayashi, K.4    Sekiya, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.