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Volumn 65, Issue 10, 2005, Pages 1666-1669

Increased incidence of genetic human prion disease in Hungary

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

EID: 28044458525     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000184513.95290.80     Document Type: Article
Times cited : (17)

References (10)
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    • EUROCJD Group. Genetic epidemiology of Creutzfeldt-Jakob disease in Europe. Rev Neurol 2001;157:633-637.
    • (2001) Rev Neurol , vol.157 , pp. 633-637
  • 4
    • 0342505312 scopus 로고    scopus 로고
    • Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
    • Lee HS, Sambuughin N, Cervenakova L, et al. Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. Am J Hum Genet 1999;64:1063-1070.
    • (1999) Am J Hum Genet , vol.64 , pp. 1063-1070
    • Lee, H.S.1    Sambuughin, N.2    Cervenakova, L.3
  • 5
    • 0035996287 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease with E200K mutation in Slovakia: Characterization and development
    • Mitrova E, Belay G. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development. Acta Virol 2002;46:31-39.
    • (2002) Acta Virol , vol.46 , pp. 31-39
    • Mitrova, E.1    Belay, G.2
  • 6
    • 0031183207 scopus 로고    scopus 로고
    • Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews
    • Baltimore
    • Meiner Z, Gabizon R, Prusiner SB. Familial Creutzfeldt-Jakob disease. Codon 200 prion disease in Libyan Jews. Medicine (Baltimore) 1997;76:227-237.
    • (1997) Medicine , vol.76 , pp. 227-237
    • Meiner, Z.1    Gabizon, R.2    Prusiner, S.B.3
  • 7
    • 0034984606 scopus 로고    scopus 로고
    • Inherited prion disease with A117V mutation of the prion protein gene: A novel Hungarian family
    • Kovacs GG, Ertsey C, Majtenyi C, et al. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family. J Neurol Neurosurg Psychiatry 2001;70:802-805.
    • (2001) J Neurol Neurosurg Psychiatry , vol.70 , pp. 802-805
    • Kovacs, G.G.1    Ertsey, C.2    Majtenyi, C.3
  • 8
    • 0347949706 scopus 로고    scopus 로고
    • Creutzfeldt-Jakob disease and inclusion body myositis: Abundant disease-associated prion protein in muscle
    • Kovacs GG, Lindeck-Pozza E, Chimelli L, et al. Creutzfeldt-Jakob disease and inclusion body myositis: abundant disease-associated prion protein in muscle. Ann Neurol 2004;55:121-125.
    • (2004) Ann Neurol , vol.55 , pp. 121-125
    • Kovacs, G.G.1    Lindeck-Pozza, E.2    Chimelli, L.3
  • 9
    • 0038452462 scopus 로고    scopus 로고
    • Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease
    • Berl
    • Jarius C, Kovacs GG, Belay G, Hainfellner JA, Mitrova E, Budka H. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease. Acta Neuropathol (Berl) 2003;105:449-454.
    • (2003) Acta Neuropathol , vol.105 , pp. 449-454
    • Jarius, C.1    Kovacs, G.G.2    Belay, G.3    Hainfellner, J.A.4    Mitrova, E.5    Budka, H.6
  • 10
    • 0343527421 scopus 로고    scopus 로고
    • A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype
    • Majtenyi C, Brown P, Cervenakova L, Goldfarb LG, Tateishi J. A three-sister sibship of Gerstmann-Straussler-Scheinker disease with a CJD phenotype. Neurology 2000;54:2133-2137.
    • (2000) Neurology , vol.54 , pp. 2133-2137
    • Majtenyi, C.1    Brown, P.2    Cervenakova, L.3    Goldfarb, L.G.4    Tateishi, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.