نتایج جستجو برای: creutzfeldt
تعداد نتایج: 3390 فیلتر نتایج به سال:
New variant Creutzfeldt-Jakob disease is a novel human prion disorder with characteristic clinical and neuropathological features, which results from exposure to the bovine spongiform encephalopathy agent. The probably lengthy incubation period makes it difficult to predict future new variant Creutzfeldt-Jakob disease case numbers; further studies are required to clarify risk factors and the po...
Creutzfeldt-Jakob disease (CJD) is a rare neurodegenerative of undetermined etiology, In syndrome the symptomatology quite variable and it consist predominantly progressive dementia with rapid onset, myoclonus, also cerebellar, pyramidal, extrapyramidal visual signs, evolution this uniformly fatal, most patients die within 12 months, we present case 72 year old women, who was admitted for statu...
Two patients with lithium toxicity presented with a neurological syndrome suggesting a diagnosis of Creutzfeldt-Jakob disease. In both cases, the initial EEG was consistent with this diagnosis. Neither patient had permanent neurological sequelae and the EEG returned to normal. A careful drug history should be taken in any patient who presents with a rapidly progressive dementia even when the EE...
Sporadic Creutzfeldt-Jakob disease is considered primarily a disease of grey matter, although the extent of white matter involvement has not been well described. We used diffusion tensor imaging to study the white matter in sporadic Creutzfeldt-Jakob disease compared to healthy control subjects and to correlated magnetic resonance imaging findings with histopathology. Twenty-six patients with s...
OBJECTIVE To identify cases of inherited prion diseases in Britain and to assess their phenotypic features. DESIGN Screening study of patients suspected clinically to have Creutzfeldt-Jakob disease and other neurodegenerative diseases by prion protein gene analysis. SETTING Biochemical research department. SUBJECTS Patients suspected to have Creutzfeldt-Jakob disease and other neurodegene...
Movement disorders presenting with parkinsonism may share histopathological features with Creutzfeldt-Jakob disease, a spongiform encephalopathy caused by the accumulation of pathological prion protein in brain. To investigate a possible aetiological link between these conditions and Creutzfeldt-Jakob disease, histoblot immunostaining for pathological prion protein was carried out in 90 cases i...
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