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1. Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions

2. Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients

3. Conserved properties of human and bovine prion strains on transmission to guinea pigs

4. Prion proteins in subpopulations of white blood cells from patients with sporadic Creutzfeldt–Jakob disease

5. Diagnosis of human prion disease

6. Mutant PrPSc conformers induced by a synthetic peptide and several prion strains

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