<p>Abbreviations: sCJD = sporadic Creutzfeldt-Jakob disease; fCJD = familial CJD; GSS = Gerstmann-straussler-Sheinker syndrome; FFI = fatal familial insomnia.</p>a<p>Difference in median survival time among multiple-group were tested by using Breslow (Wilcoxon) method.</p>b<p>Difference in median survival time between two groups were tested by using log-rank (Mantel-Cox) method.</p
Progress in therapeutics for rare disorders like prion disease is impeded by the lack of validated o...
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal, neurodegenerative disease caused by accu...
Human prion diseases are a group of rare neurodegenerative disorders characterized by the conversion...
textabstractA collaborative study of human transmissible spongiform encephalopathies has been carrie...
Prion diseases are kinds of progressive, incurable neurodegenerative disorders. So far, survival tim...
International audienceSporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of prion dis...
<p>A. Distribution of the age of onset based upon the types of disease. The median onset age of all ...
This study examined trends in mortality from sporadic Creutzfeldt-Jakob disease in France for 1992–7...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
a<p>Periodic sharp curve complexes.</p>b<p>Electroencephalograms.</p>c<p>Magnatic Resonance Imaging ...
subtypes or a spectrum of disease? Although the condition we now call sporadic Creutzfeldt–Jakob dis...
Prion diseases or transmissible spongiform encephalopathies (TSE) are a group of neurodegenerative d...
Prion diseases are unique transmissible neurodegenerative diseases that have diverse phenotypes and ...
Introduction. Fatal familial insomnia (FFI) is one of the transmissible spongiform encephathalopathi...
Progress in therapeutics for rare disorders like prion disease is impeded by the lack of validated o...
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal, neurodegenerative disease caused by accu...
Human prion diseases are a group of rare neurodegenerative disorders characterized by the conversion...
textabstractA collaborative study of human transmissible spongiform encephalopathies has been carrie...
Prion diseases are kinds of progressive, incurable neurodegenerative disorders. So far, survival tim...
International audienceSporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of prion dis...
<p>A. Distribution of the age of onset based upon the types of disease. The median onset age of all ...
This study examined trends in mortality from sporadic Creutzfeldt-Jakob disease in France for 1992–7...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
a<p>Periodic sharp curve complexes.</p>b<p>Electroencephalograms.</p>c<p>Magnatic Resonance Imaging ...
subtypes or a spectrum of disease? Although the condition we now call sporadic Creutzfeldt–Jakob dis...
Prion diseases or transmissible spongiform encephalopathies (TSE) are a group of neurodegenerative d...
Prion diseases are unique transmissible neurodegenerative diseases that have diverse phenotypes and ...
Introduction. Fatal familial insomnia (FFI) is one of the transmissible spongiform encephathalopathi...
Progress in therapeutics for rare disorders like prion disease is impeded by the lack of validated o...
Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare, fatal, neurodegenerative disease caused by accu...
Human prion diseases are a group of rare neurodegenerative disorders characterized by the conversion...