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Mortuary rites of the South Fore and kuru
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Bjoern Seidel et al.
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Stephen J. Wroe et al.
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M Tanaka et al.
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Possible transmission of variant Creutzfeldt-Jakob disease by blood transfusion
CA Llewelyn et al.
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AH Peden et al.
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M Glatzel et al.
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Familial and sporadic fatal insomnia
P Montagna et al.
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Tissue distribution of protease resistant prion protein in variant Creutzfeldt-Jakob disease using a highly sensitive immunoblotting assay
JDF Wadsworth et al.
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Iatrogenic Creutzfeldt-Jakob disease at the millennium
P Brown et al.
NEUROLOGY (2000)
High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes
U Finckh et al.
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