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Genetic Creutzfeldt–Jakob disease
2018Genetic Creutzfeldt-Jakob disease (CJD) is associated with mutations in the human PrP gene (PRNP) on chromosome 20p12-pter. Pathogenic mutations have been identified in 10-15% of all CJD patients, who often have a family history of autosomal-dominant pattern of inheritance and variable penetrance.
Anna, Ladogana, Gabor G, Kovacs
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Variant Creutzfeldt-Jakob disease
The Lancet, 1999It is clear that the prion strain causing bovine spongiform encephalopathy (BSE) in cattle has infected human beings, manifesting itself as a novel human prion disease, variant Creutzfeldt-Jakob disease (CjD). Studies of the incubation periods seen in previous epidemics of human prion disease and of the effect of transmission barriers limiting spread ...
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Anakinra in Creutzfeldt-Jakob disease
Acta Neurologica Belgica, 2022Giuseppe Bomboi +4 more
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A new variant of Creutzfeldt-Jakob disease in the UK
Lancet, The, 1996R G Will, J W Ironside, M Zeidler
exaly