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pubmed-article:14602879pubmed:abstractTextIn patients with sporadic Creutzfeldt-Jakob disease, pathologic disease-associated prion protein (PrPSc) has been identified only in the central nervous system and olfactory-nerve tissue. Understanding the distribution of PrPSc in Creutzfeldt-Jakob disease is important for classification and diagnosis and perhaps even for prevention.lld:pubmed
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pubmed-article:14602879pubmed:articleTitleExtraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.lld:pubmed
pubmed-article:14602879pubmed:affiliationInstitute of Neuropathology and National Reference Center for Prion Diseases, University Hospital of Zurich, Zurich, Switzerland.lld:pubmed
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