Review: Laboratory diagnosis and surveillance of Creutzfeldt-Jakob disease

Creutzfeldt–Jakob disease (CJD) is a representative human transmissible spongiform encephalopathy associated with central nervous system degeneration. Prions, the causative agents of CJD, are composed of misfolded prion proteins and are able to self‐replicate. While CJD is a rare disease affecting o...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Journal of medical virology 2015-01, Vol.87 (1), p.175-186
Hauptverfasser:	Lee, Jeongmin, Hyeon, Jae Wook, Kim, Su Yeon, Hwang, Kyu-Jam, Ju, Young Ran, Ryou, Chongsuk
Format:	Artikel
Sprache:	eng
Schlagworte:	Clinical Laboratory Techniques - methods Creutzfeldt-Jakob disease Creutzfeldt-Jakob Syndrome - diagnosis Creutzfeldt-Jakob Syndrome - epidemiology diagnosis Epidemiological Monitoring Humans Medical diagnosis prion disease Surveillance transmissible spongiform encephalopathy Virology
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!