Creutzfeldt-Jakob disease (CJD) is a fatal disease caused by the accumulation of abnormal prion proteins in neurological tissues. Routine notification data reveal that NSW has similar rates of CJD to other states and territories in Australia; however, it is likely that there is significant under-ascertainment of cases. It is important that clinicians and public health staff remain vigilant for the clinical signs of CJD and understand the limitations of the different diagnostic tests available. This paper provides a brief overview of the epidemiology of CJD in NSW, as well as current issues in the diagnosis and public health investigation of CJD
Creutzfeldt-Jakob disease (CJD) is a representative human transmissible spongiform encephalopathy as...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) is a transmissible disorder of the central n...
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission ...
Nationwide surveillance of Creutzfeldt-Jakob disease and other human prion diseases is performed by ...
INTRODUCTION: Creutzfeldt-Jakob disease (CJD), a spongiform encephalopathy, caused by a transmissibl...
The Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR) commenced surveillance in Septem...
Creutzfeldt-Jakob disease (CJD) is a rare prion disorder that has been the subject of both professio...
BACKGROUND: Prion diseases are a family of rare, progressive, neurodegenerative disorders that affec...
Variant Creutzfeldt-Jakob disease (vCJD) was identified as a new disease in 1996. It was linked to i...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Variant Creutzfeldt–Jakob disease (vCJD) is a transmissible neurodegenerative prion disease that con...
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission ...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creutzfeldt-Jakob disease (CJD) is a rare, slowly degenerating, viral disease that attacks the centr...
Variant Creutzfeldt-Jakob disease (vCJD) was identified as a new disease in 1996. It was linked to i...
Creutzfeldt-Jakob disease (CJD) is a representative human transmissible spongiform encephalopathy as...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) is a transmissible disorder of the central n...
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission ...
Nationwide surveillance of Creutzfeldt-Jakob disease and other human prion diseases is performed by ...
INTRODUCTION: Creutzfeldt-Jakob disease (CJD), a spongiform encephalopathy, caused by a transmissibl...
The Australian National Creutzfeldt-Jakob Disease Registry (ANCJDR) commenced surveillance in Septem...
Creutzfeldt-Jakob disease (CJD) is a rare prion disorder that has been the subject of both professio...
BACKGROUND: Prion diseases are a family of rare, progressive, neurodegenerative disorders that affec...
Variant Creutzfeldt-Jakob disease (vCJD) was identified as a new disease in 1996. It was linked to i...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Variant Creutzfeldt–Jakob disease (vCJD) is a transmissible neurodegenerative prion disease that con...
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission ...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creutzfeldt-Jakob disease (CJD) is a rare, slowly degenerating, viral disease that attacks the centr...
Variant Creutzfeldt-Jakob disease (vCJD) was identified as a new disease in 1996. It was linked to i...
Creutzfeldt-Jakob disease (CJD) is a representative human transmissible spongiform encephalopathy as...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) is a transmissible disorder of the central n...
Variant Creutzfeldt-Jakob disease (vCJD) is a rare, fatal prion disease resulting from transmission ...