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Works
8
Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.
Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification
Human prion diseases
Tribute to Robert Terry
New topics in familial prion diseases
Sporadic and familial CJD: classification and characterisation.
Prion Diseases and Dementia
Genetic Creutzfeldt-Jakob Disease
