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Folia Neuropathol. 2000;38(4):151-60.

The diagnosis of human prion diseases.

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1
Department of Pathology, Chair of Oncology, Medical University, Lódź, Poland. radekkordek@interia.pl

Abstract

Prion diseases present a wide spectrum of clinical and neuropathological features. In this review, clinical and neuropathological findings are summarized along with criteria for the diagnosis of the molecular-phenotypic subtypes of sporadic Creutzfeldt-Jakob disease (CJD), familial CJD, new variant CJD, iatrogenic CJD, Gerstmann-Straussler-Scheinker disease, fatal familial insomnia and kuru.

PMID:
11693717
[Indexed for MEDLINE]
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