7 results on '"Windl, Otto"'
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2. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment
3. Loss of glycosylation associated with the T183A mutation in human prion disease
4. Iatrogenic Creutzfeldt-Jakob Disease with Florid Plaques
5. Clinical findings in sporadic Creutzfeldt–Jakob disease correlate with thalamic pathology
6. The Heidenhain Variant of Creutzfeldt-Jakob Disease
7. Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluid
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