A refined method for molecular typing reveals that co-occurrence of PrPSc types in Creutzfeldt–Jakob disease is not the rule - Notari, Silvio; Capellari, Sabina; Langeveld, Jan; Giese, Armin; Strammiello, Rosaria; Gambetti, Pierluigi; Kretzschmar, Hans A; Parchi, Piero (Laboratory investigation, 2007)
Keywords: abnormal prion protein; agent; Biological and medical sciences; Biotechnology; bovine spongiform encephalopathy; classification; fatal familial insomnia; Fundamental and applied biological sciences. Psychology; Investigative techniques, diagnostic techniques (general aspects); Laboratory Medicine; Medical sciences; Medicine; Medicine & Public Health; mice; monoclonal-antibodies; Pathology; prion; research-article; scrapie strains; sheep; strain; typing; variant cjd; western blotting; strain; typing; prion; western blotting; classification; Biotechnology; Prion disease; Nervous system diseases; Typing; Creutzfeldt-Jakob disease; Cerebral disorder; Strain; Infection; Central nervous system disease; Clinical biology; Classification; Immunoblotting assay; Degenerative disease; Prion