Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66084/1/j.1600-0404.1968.tb07440.x.pd
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that affects about 1 in 10(6) inhabit...
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD usuall...
Creutzfeldt-Jakob disease has a higher incidence in Chile than in other countries. The post mortem ...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt-Jakob disease (CJD) is the most common type of human prion disease. Similarly to other p...
Creutzfeldt and Jakob's disease (CJD) has its initial milestone in the publication issued 100 years ...
Creutefeldt-].akob disease is afata l degenerative disorder ofthe central nervous system. The variab...
Creutzfeldt-Jakob disease (CJD) is a rare type of prion disease leading to a rapidly progressive dem...
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish t...
ObjectivesTo identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) du...
Creutzfeldt-Jakob disease is lethal and most common spongiform encephalopathy worldwide and is rarel...
In 1920, H.G. Creutzfeldt (then working in Alzheimers laboratory) published the case of a 22-year-ol...
Creutzfeldt-Jakob disease (CJD) is a rare cause of rapidly progressive dementia, it is a neurodegene...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that affects about 1 in 10(6) inhabit...
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD usuall...
Creutzfeldt-Jakob disease has a higher incidence in Chile than in other countries. The post mortem ...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt-Jakob disease (CJD) is the most common type of human prion disease. Similarly to other p...
Creutzfeldt and Jakob's disease (CJD) has its initial milestone in the publication issued 100 years ...
Creutefeldt-].akob disease is afata l degenerative disorder ofthe central nervous system. The variab...
Creutzfeldt-Jakob disease (CJD) is a rare type of prion disease leading to a rapidly progressive dem...
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish t...
ObjectivesTo identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) du...
Creutzfeldt-Jakob disease is lethal and most common spongiform encephalopathy worldwide and is rarel...
In 1920, H.G. Creutzfeldt (then working in Alzheimers laboratory) published the case of a 22-year-ol...
Creutzfeldt-Jakob disease (CJD) is a rare cause of rapidly progressive dementia, it is a neurodegene...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy that affects about 1 in 10(6) inhabit...
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD usuall...
Creutzfeldt-Jakob disease has a higher incidence in Chile than in other countries. The post mortem ...
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