n.rare (usually fatal) brain disease (usually in middle age) caused by an unidentified slow virus; characterized by progressive dementia and gradual loss of muscle control

同義詞：CJDJakob-Creutzfeldt disease

Creutzfeldt-Jakob Disease Associated with Cadaveric Dura Mater Grafts — Japan, January 1979–May 1996
CREUTZFELDT-JAKOB DISEASE
Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study.
A new variant of Creutzfeldt-Jakob disease in the UK.
Incidence of variant Creutzfeldt-Jakob disease in the UK.
Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion.
Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism
Diagnosis of new variant Creutzfeldt-Jakob disease by tonsil biopsy.
Iatrogenic Creutzfeldt-Jakob disease at the millennium.