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Showing articles 0 to 3 of 3 Filter Applied: prion disease (Click to remove) Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene NEJM 326:444-449, Medori,R.,et al, 1992 Prion Dementia Without Characteristic Pathology Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990 Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis Lancet 2:15-17, Collinge,J.,et al, 1989 Showing articles 0 to 3 of 3