Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt–Jakob disease

Background: Immunocytochemical accumulation of prion protein (PrP) in lymphoid tissues is a feature of variant Creutzfeldt–Jakob disease (vCJD) that has been used both to aid in the diagnosis of patients and as a basis of large scale screening studies to assess the prevalence of preclinical disease...

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Autores principales: Hilton, D A, Sutak, J, Smith, M E F, Penney, M, Conyers, L, Edwards, P, McCardle, L, Ritchie, D, Head, M W, Wiley, C A, Ironside, J W
Formato: Artigo
Lenguaje:Inglês
Publicado: Copyright 2004 Journal of Clinical Pathology 2004
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Original Articles
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC1770247/
https://ncbi.nlm.nih.gov/pubmed/14990604
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jcp.2003.012278
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