Few issues in neuroimaging are as controversial as the nomenclature used to describe
abnormalities of the lumbosacral spine. What immediately comes to mind are the variations …

ABSTRACT INTRODUCTION Creutzfeldt‐Jakob disease (CJD) is a rapidly progressive
dementia with a median survival of 2‐14 months. The diagnosis can only be made …

A 72-year-old woman presented 6 months after the onset of falls and ataxia, which had
progressed to wheelchair dependence, followed by the onset of bizarre behavior and rapid …

DISCUSSION Creutzfeldt-Jakob disease (CJD) is a rare but invariably fatal
neurodegenerative illness caused by accumulation of an abnormal form of a PrP, or prion, in …

Creutzfeldt-Jakob Disease (CJD) typically causes a rapidly progressive dementia that may
be associated with other neurologic features such as cerebellar or visual disturbance. New …

A 75-year-old woman with unremarkable medical history, consulted for a 5-month history of
involuntary shaking of left upper limb. Clinical examination revealed polyminimyoclonus of …

Creutzfeldt‐Jakob disease (CJD) causes diffuse neurological symptoms, but asymmetric
lesions have been found on conventional magnetic resonance imaging (MRI) and diffusion …

Creutzfeldt–Jakob disease (CJD) is a rare spongiform encephalopathy that usually affects
elderly people, and it is clinically characterized by rapidly progressive dementia and …

Creutzfeldt–Jakob Disease (CJD) is a rare, progressive and invariably fatal
neurodegenerative disease characterized by specific histopathological features. Of the four …

A 59-year-old woman presented with a 2-month history of headache, difficulty in finding
words, and slow speech. Those symptoms were associated with intermittent bilateral jerky …