INTRODUCTION: The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confirmation. To date, diagnosis has relied upon the finding of the biomarkers 14-3-3 protein and total tau (t-tau) protein in the cerebrospinal fluid (CSF), but many researchers have reported that these markers are not sufficiently elevated in gPrD, especially in Gerstmann-Sträussler-Scheinker syndrome (GSS). We recently developed a new in vitro amplification technology, designated "real-time quaking-induced conversion (RT-QUIC)", to detect the abnormal form of prion protein in CSF from sporadic Creutzfeldt-Jakob disease (sCJD) patients. In the present study, we aimed to investigate the presence of biomarkers and evaluate RT-QUIC assay in patients...
The differential diagnosis of Creutzfeldt-Jakob disease (CJD) from other, sometimes treatable, neuro...
Fast, definitive diagnosis of Creutzfeldt-Jakob disease (CJD) is important in assessing patient care...
ABSTRACT A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion disea...
Introduction: The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confir...
Introduction: The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confir...
Until recently, it has been difficult to detect all infectious levels of prions and diagnose prion d...
Importance: Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary fo...
Objective: We present the National Prion Disease Pathology Surveillance Center's (NPDPSC) experienc...
An early and accurate in vivo diagnosis of rapidly progressive dementia remains challenging, despite...
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and fatal neurodegenerative disorder with an inc...
ABSTRACT Fast, definitive diagnosis of Creutzfeldt-Jakob disease (CJD) is important in assessing pat...
Early and accurate diagnosis of Creutzfeldt-Jakob disease (CJD) is a necessary to distinguish this u...
Real-time quaking-induced conversion (RT-QuIC) allows the amplification of miniscule amounts of scra...
A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion diseases in me...
The development of technologies for the in vitro amplification of abnormal conformations of prion pr...
The differential diagnosis of Creutzfeldt-Jakob disease (CJD) from other, sometimes treatable, neuro...
Fast, definitive diagnosis of Creutzfeldt-Jakob disease (CJD) is important in assessing patient care...
ABSTRACT A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion disea...
Introduction: The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confir...
Introduction: The definitive diagnosis of genetic prion diseases (gPrD) requires pathological confir...
Until recently, it has been difficult to detect all infectious levels of prions and diagnose prion d...
Importance: Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary fo...
Objective: We present the National Prion Disease Pathology Surveillance Center's (NPDPSC) experienc...
An early and accurate in vivo diagnosis of rapidly progressive dementia remains challenging, despite...
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare and fatal neurodegenerative disorder with an inc...
ABSTRACT Fast, definitive diagnosis of Creutzfeldt-Jakob disease (CJD) is important in assessing pat...
Early and accurate diagnosis of Creutzfeldt-Jakob disease (CJD) is a necessary to distinguish this u...
Real-time quaking-induced conversion (RT-QuIC) allows the amplification of miniscule amounts of scra...
A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion diseases in me...
The development of technologies for the in vitro amplification of abnormal conformations of prion pr...
The differential diagnosis of Creutzfeldt-Jakob disease (CJD) from other, sometimes treatable, neuro...
Fast, definitive diagnosis of Creutzfeldt-Jakob disease (CJD) is important in assessing patient care...
ABSTRACT A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion disea...