Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob disease

Sporadic Creutzfeldt-Jakob disease is a fatal neurodegenerative disease caused by misfolded prion proteins (PrPSc). Effective therapeutics are currently not available and accurate diagnosis can be challenging. Clinical diagnostic criteria use a combination of characteristic neuropsychiatric symptoms...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Lancet neurology 2021-03, Vol.20 (3), p.235-246
Hauptverfasser:	Hermann, Peter, Appleby, Brian, Brandel, Jean-Philippe, Caughey, Byron, Collins, Steven, Geschwind, Michael D, Green, Alison, Haïk, Stephane, Kovacs, Gabor G, Ladogana, Anna, Llorens, Franc, Mead, Simon, Nishida, Noriyuki, Pal, Suvankar, Parchi, Piero, Pocchiari, Maurizio, Satoh, Katsuya, Zanusso, Gianluigi, Zerr, Inga
Format:	Artikel
Sprache:	eng
Schlagworte:	14-3-3 protein Accuracy Biomarkers Biomarkers - analysis Biopsy Bovine spongiform encephalopathy Cerebrospinal fluid Clinical medicine Creutzfeldt-Jakob disease Creutzfeldt-Jakob Syndrome - diagnosis Creutzfeldt-Jakob Syndrome - diagnostic imaging Creutzfeldt-Jakob Syndrome - genetics Dementia Diagnosis Diagnostic tests EEG Encephalitis Genetic Markers Guidelines as Topic Humans Magnetic resonance imaging Medical diagnosis Neurodegenerative diseases Neuroimaging Neuropathology Polymorphism Protein interaction Protein seeding Proteins Sensitivity and Specificity Surveillance Tau protein
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!