2006年8月21日 · Methods: CSF was tested for 14-3-3, Tau, NSE, and S100b in 1,859 patients with sporadic, genetic, iatrogenic, and variant CJD, and in 1,117 controls. Results: The highest …

2024年1月30日 · Creutzfeldt-Jakob disease (CJD) is a rare, fatal degenerative brain disorder caused by prion proteins. This condition belongs to a group of transmissible spongiform …

Patients with suspected Creutzfeldt-Jakob disease (CJD) often have routine cerebrospinal fluid (CSF) analysis performed to exclude treatable inflammatory conditions; however, little …

The prion protein disorder Creutzfeldt-Jakob disease (CJD) is a human transmissible spongiform encephalopathy (TSE) that leads to rapid decay of brain tissue. Human prion diseases are …

2022年4月21日 · Creutzfeldt-Jakob disease (CJD) is a severe, degenerative brain condition. It happens when faulty proteins, known as prions, damage your brain. This condition usually …

2024年12月15日 · CJD is a fatal prior disease with rapid progression, affecting 1–2 per million annually, with no cure. Types include sporadic, familial, and acquired CJD, sporadic is the …

CSF RT-QuIC has a superior sensitivity and specificity for the diagnosis of sporadic CJD when compared to other CSF biomarkers including CSF 14-3-3. In our hands the sensitivity and …

2022年4月6日 · The diagnosis of Creutzfeldt–Jakob disease has advanced from detection of characteristic EEG and MRI features to include the detection in CSF of 14-3-3 protein and, …

2006年8月22日 · Objectives: To analyze the diagnostic sensitivity and specificity of various brain-derived proteins (14-3-3, Tau, neuron specific enolase [NSE], and S100b) in the CSF of …

May aid in the diagnosis of Creutzfeldt-Jakob disease (CJD). This test uses qualitative real-time quaking-induced conversion to identify the causative agent of CJD, and also includes indirect …