Add to ORKGIntroduction: 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 flui
The diagnostics of prion diseases, including Creutzfeldt-Jakob disease (CJD), is still challenging a...
Human prion diseases can be sporadic, inherited, or acquired by infection. Distinct clinical and pat...
Early and accurate diagnosis of Creutzfeldt-Jakob disease (CJD) is a necessary to distinguish this u...
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...
Prion diseases are progressive and irreversible neurodegenerative disorders with a low incidence (1....
Protein amplification techniques exploit the ability of PrPTSE to induce a conformational change in ...
The human prion diseases are a diverse set of often rapidly progressive neurodegenerative conditions...
Objective: We present the National Prion Disease Pathology Surveillance Center's (NPDPSC) experienc...
Prion diseases, synucleinopathies and tauopathies are neurodegenerative disorders characterized by d...
The protease resistant isoform of prion protein (PrP) is a diagnostic marker of spongiform encephalo...
Transmissible spongiform encephalopathies or prion diseases are rapidly progressive neurodegenerativ...
Importance: Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary fo...
A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion diseases in me...
The diagnostics of prion diseases, including Creutzfeldt-Jakob disease (CJD), is still challenging a...
Human prion diseases can be sporadic, inherited, or acquired by infection. Distinct clinical and pat...
Early and accurate diagnosis of Creutzfeldt-Jakob disease (CJD) is a necessary to distinguish this u...
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...
Prion diseases are progressive and irreversible neurodegenerative disorders with a low incidence (1....
Protein amplification techniques exploit the ability of PrPTSE to induce a conformational change in ...
The human prion diseases are a diverse set of often rapidly progressive neurodegenerative conditions...
Objective: We present the National Prion Disease Pathology Surveillance Center's (NPDPSC) experienc...
Prion diseases, synucleinopathies and tauopathies are neurodegenerative disorders characterized by d...
The protease resistant isoform of prion protein (PrP) is a diagnostic marker of spongiform encephalo...
Transmissible spongiform encephalopathies or prion diseases are rapidly progressive neurodegenerativ...
Importance: Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary fo...
A key challenge in managing transmissible spongiform encephalopathies (TSEs) or prion diseases in me...
The diagnostics of prion diseases, including Creutzfeldt-Jakob disease (CJD), is still challenging a...
Human prion diseases can be sporadic, inherited, or acquired by infection. Distinct clinical and pat...
Early and accurate diagnosis of Creutzfeldt-Jakob disease (CJD) is a necessary to distinguish this u...