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Sporadic CJD

National Institutes of Health

Papers overview

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Review
2017
Review
2017
Definitive diagnosis of Creutzfeldt Jakob disease (CJD) remains tissue-based. Possible and probable CJD are useful clinical terms… 
2014
2014
It is widely believed that host prion protein (PrP), without nucleic acid, converts itself into an infectious form (PrP‐res) that… 
2011
2011
One of the largest clusters of genetic Creutzfeldt–Jakob disease (gCJD) is found among Jews of Libyan origin in Israel and is… 
2008
2008
A recent paper reported the in vitro generation of new prion strains, supporting the idea that 'strain-ness' is encoded in the… 
2005
2005
We report here a detailed ultrastructural comparison of brain biopsies from 13 cases of Creutzfeldt‐Jakob disease (CJD) and from… 
2005
2005
After the finding that anti-prion antibodies stain sensory and sympathetic ganglia in variant Creutzfeldt-Jakob disease (vCJD… 
2002
2002
JNNP could help you become a technophile It is possible to thrive in the modern world without recourse to the internet. But only… 
2001
2001
Objective: To describe the clinical and neuropathologic profile and determine the strain characteristics of familial Creutzfeldt…