Sporadic CJD
National Institutes of Health
Papers overview
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Definitive diagnosis of Creutzfeldt Jakob disease (CJD) remains tissue-based. Possible and probable CJD are useful clinical terms…
It is widely believed that host prion protein (PrP), without nucleic acid, converts itself into an infectious form (PrP‐res) that…
One of the largest clusters of genetic Creutzfeldt–Jakob disease (gCJD) is found among Jews of Libyan origin in Israel and is…
A recent paper reported the in vitro generation of new prion strains, supporting the idea that 'strain-ness' is encoded in the…
We report here a detailed ultrastructural comparison of brain biopsies from 13 cases of Creutzfeldt‐Jakob disease (CJD) and from…
After the finding that anti-prion antibodies stain sensory and sympathetic ganglia in variant Creutzfeldt-Jakob disease (vCJD…
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Objective: To describe the clinical and neuropathologic profile and determine the strain characteristics of familial Creutzfeldt…