Cerebrospinal fluid markers in the differentiation of molecular subtypes of sporadic Creutzfeldt−Jakob disease

Cerebrospinal fluid tau levels are a marker for molecular subtype in sporadic Creutzfeldt-Jakob disease

(2015) André Karch et al.   NEUROBIOLOGY OF AGING

Subtype and regional regulation of prion biomarkers in sporadic Creutzfeldt-Jakob disease

(2015) Franc Llorens et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Subtype and Regional-Specific Neuroinflammation in Sporadic Creutzfeldt–Jakob Disease

(2014) Franc Llorens et al.   Frontiers in Aging Neuroscience

Diagnostic Performance of Cerebrospinal Fluid Total Tau and Phosphorylated Tau in Creutzfeldt-Jakob Disease

(2014) Tobias Skillbäck et al.   JAMA Neurology

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

(2012) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

Thorough work-up and new diagnostic criteria needed for CJD

(2011) David C. Perry et al.   Nature Reviews Neurology

Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification

(2009) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

The diagnostic efficiency of biomarkers in sporadic Creutzfeldt-Jakob disease compared to Alzheimer's disease

(2008) Justyna Maria Czarna Bahl et al.   NEUROBIOLOGY OF AGING

14-3-3 CSF levels in sporadic Creutzfeldt–Jakob disease differ across molecular subtypes

(2008) K. Gmitterová et al.   NEUROBIOLOGY OF AGING