| Document Date: 2012-11-05 04:56:25
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Country United Kingdom / / MedicalCondition ataxia / cerebellar ataxia / Human Prion Diseases / incoordination / genetic CJD / neurological illness / myoclonus / brain dysfunction / relatively longer disease / iatrogenic disease / dementia / disease / headache / human prion disease / sporadic CJD / Iatrogenic CJD / short illness / Fatal Familial Insomnia / hallucinations / CJD / Prion Disease / chorea / progressive cerebellar syndrome / GENETIC PRION DISEASES These diseases / Prion diseases / progressive neuropsychiatric disorder / genetic prion disease / CLINICAL FEATURES OF HUMAN PRION DISEASES / diseases / Variant CJD / Certain involuntary movements / Gerstmann Sträussler Scheinker syndrome / rapidly progressive dementia / infection / progressive cerebellar ataxia / dystonia / main illness / illness / tiredness / Genetic Prion Diseases / depression / blindness / Epileptic seizures / develop including chorea / / MedicalTreatment neurosurgery / / Technology neurosurgery / /
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THE CLINICAL FEATURES OF HUMAN PRION DISEASES: