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Volumn 132, Issue 10, 2009, Pages 2627-2629

Sporadic Creutzfeldt-Jakob disease: Discrete subtypes or a spectrum of disease

Author keywords

[No Author keywords available]

Indexed keywords

PRION PROTEIN;

EID: 70349952066     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awp225     Document Type: Note
Times cited : (9)

References (12)
  • 1
    • 70349937836 scopus 로고    scopus 로고
    • Co-existence of scrapie prion protein types 1 and 25 in sporadic Creutzfeldt-Jakob disease: Its effect on the phenotype and prion-type characteristics
    • doi:10.1093/brain/awp196. Published online 04 September 2009
    • Cali I, Castellani R, Alshekhlee A, Cohen Y, Blevins J, Yuan J, et al. Co-existence of scrapie prion protein types 1 and 25 in sporadic Creutzfeldt-Jakob disease: its effect on the phenotype and prion-type characteristics. Brain. doi:10.1093/brain/awp196. Published online 04 September 2009.
    • Brain
    • Cali, I.1    Castellani, R.2    Alshekhlee, A.3    Cohen, Y.4    Blevins, J.5    Yuan, J.6
  • 2
    • 2542618458 scopus 로고    scopus 로고
    • Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: United Kingdom Cases 1991-2002
    • Head MW, Bunn TJR, Bishop MT, McLoughlin V, Lowrie S, McKimmie CS, et al. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: United Kingdom Cases 1991-2002. Ann Neurol 2004; 55: 851-859
    • (2004) Ann Neurol , vol.55 , pp. 851-859
    • Head, M.W.1    Bunn, T.J.R.2    Bishop, M.T.3    McLoughlin, V.4    Lowrie, S.5    McKimmie, C.S.6    Al, E.7
  • 4
    • 35348941241 scopus 로고    scopus 로고
    • A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt-Jakob disease is not the rule
    • Notari S, Capellari S, Langeveld J, Giese A, Strammiello R, Gambetti P, et al. A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt-Jakob disease is not the rule. Lab Invest 2007; 87: 1103-1112
    • (2007) Lab Invest , vol.87 , pp. 1103-1112
    • Notari, S.1    Capellari, S.2    Langeveld, J.3    Giese, A.4    Strammiello, R.5    Gambetti, P.6
  • 5
    • 0032816292 scopus 로고    scopus 로고
    • Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects
    • Parchi P, Giese A, Capellari S, Brown P, Schulz-Schaeffer W, Windl O, et al. Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects. Ann Neurol 1999; 46: 224-233
    • (1999) Ann Neurol , vol.46 , pp. 224-233
    • Parchi, P.1    Giese, A.2    Capellari, S.3    Brown, P.4    Schulz-Schaeffer, W.5    Windl, O.6
  • 12
    • 67650630953 scopus 로고    scopus 로고
    • Further characterization of the prion protein molecular types in the NIBSC Creutzfeldt-Jakob disease brain reference materials
    • Yull HM, Ironside JW, Head MW. Further characterization of the prion protein molecular types in the NIBSC Creutzfeldt-Jakob disease brain reference materials. Biologicals 2009; 37: 210-215
    • (2009) Biologicals , vol.37 , pp. 210-215
    • Yull, H.M.1    Ironside, J.W.2    Head, M.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.