Add to ORKGABSTRACT- Creutzfeldt-Jakob disease (CJD) is a transmissible disease of the nervous system causatively related to the presence of an abnormal prion protein, with dementia, myoclonic jerks, and periodic EEG activity. Fourteen patients (7 females and 7 males) ranging from 26 to 76 years of age (median 59 years) were evaluate
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creuzfeldt-Jakobs Disease is a rare neurodegenerative disorder that is included among the transmissi...
Background: Creutzfeldt-Jakob disease (CJD) as a life-threatening neurodegenerative disorder is not ...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Creutzfeldt-Jacob Disease is a prion disease which has a wide range of clinical presentations. Its d...
Creutzfeldt-Jakob disease (CJD) is a rare, fatal neurodegenerative disease caused by an infectious p...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt- Jakob Disease (OD) is a rare, slowly degenerating, viral disease that attacks the centr...
Creutzfeldt-Jakob disease (CJD) is a progressive, degenerative, and fatal disease of the central ner...
Creutzfeldt-Jakob disease (CJD) is the most common type of human prion disease. Similarly to other p...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
Creutzfeldt–Jakob disease (CJD) is a rare neurodegenerative disease caused by the accumulation of th...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creutzfeldt-Jakob Disease (CJD) is a rare invariably fatal neurodegenerative disease believed to be ...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creuzfeldt-Jakobs Disease is a rare neurodegenerative disorder that is included among the transmissi...
Background: Creutzfeldt-Jakob disease (CJD) as a life-threatening neurodegenerative disorder is not ...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Creutzfeldt-Jacob Disease is a prion disease which has a wide range of clinical presentations. Its d...
Creutzfeldt-Jakob disease (CJD) is a rare, fatal neurodegenerative disease caused by an infectious p...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt- Jakob Disease (OD) is a rare, slowly degenerating, viral disease that attacks the centr...
Creutzfeldt-Jakob disease (CJD) is a progressive, degenerative, and fatal disease of the central ner...
Creutzfeldt-Jakob disease (CJD) is the most common type of human prion disease. Similarly to other p...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
Creutzfeldt–Jakob disease (CJD) is a rare neurodegenerative disease caused by the accumulation of th...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creutzfeldt-Jakob Disease (CJD) is a rare invariably fatal neurodegenerative disease believed to be ...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Creuzfeldt-Jakobs Disease is a rare neurodegenerative disorder that is included among the transmissi...
Background: Creutzfeldt-Jakob disease (CJD) as a life-threatening neurodegenerative disorder is not ...