New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome

Karen Hsiao, Harry F. Baker, Tim Crow et al. · Nature · 1989 · 843 citations

Creutzfeldt-jakob Disease, Genetic Disorder, Genetics +9

Fatal Familial Insomnia and Familial Creutzfeldt-Jakob Disease: Disease Phenotype Determined by a DNA Polymorphism

Lev G. Goldfarb, Robert B. Petersen, Massimo Tabaton et al. · Science · 1992 · 716 citations

Fatal Familial Insomnia, a Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene

Rossella Medori, Hans-Juergen Tritschler, Andréa LeBlanc et al. · New England Journal of Medicine · 1992 · 606 citations · Full text

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

Tetsuyuki Kitamoto, Tamaki Muramoto, Satoshi Mohri et al. · Journal of Virology · 1991 · 289 citations · Full text

Creutzfeldt-jakob Disease, Immunodeficiencies, Immunology +18

Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease.

Tetsuyuki Kitamoto, R W Shin, Katsumi Doh‐ura et al. · PubMed · 1992 · 270 citations · Full text