Prion diseases

Amos D. Korczyn*

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review


Prion diseases are a group of disorders sharing clinical and pathological features. Many of the enigmas of these diseases have now yielded to the concerted effort to understand them and their unusual pathogenesis. The genetic backgrounds of the various diseases are being clarified at an impressive rate, but the cause of sporadic Creutzfeldt-Jakob disease, the most frequently occurring human prion disease, is still not understood at all. The mechanisms underlying the evolution of the disease, as well as the species barrier, are better understood.

Original languageEnglish
Pages (from-to)273-281
Number of pages9
JournalCurrent Opinion in Neurology
Issue number3
StatePublished - 1997


Dive into the research topics of 'Prion diseases'. Together they form a unique fingerprint.

Cite this