Sporadic Creutzfeldt–Jakob Disease

Sporadic Creutzfeldt–Jakob disease is the most frequent human prion disease, with a yearly mortality of between one and two cases per million. It is usually assumed that it arises spontaneously, i.e. for no obvious cause. Neuropathological examination has remained the most important tool for a defin...

Ausführliche Beschreibung

Bibliographische Detailangaben

Hauptverfasser:	Budka, Herbert, Head, Mark W, Ironside, James W, Gambetti, Pierluigi, Parchi, Piero, Tagliavini, Fabrizio
Format:	Buchkapitel
Sprache:	eng
Schlagworte:	Creutzfeldt–Jakob disease genetic polymorphism immunoblotting immunohistochemistry neuropathology prion protein prion protein gene transmissible spongiform encephalopathy
Online-Zugang:	Volltext
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