Diversity of prion diseases: (no) strains attached? Sebastian Brandner Editorial 16 November 2010 Pages: 1 - 4
Tau, prions and Aβ: the triad of neurodegeneration Lilla ReinigerAna LukicSebastian Brandner Review Open access 16 May 2010 Pages: 5 - 20
Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis Sabina CapellariRosaria StrammielloPiero Parchi Review 27 October 2010 Pages: 21 - 37
Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy Gabor G. KovacsJérémie SeguinArmand Perret-Liaudet Original Paper 01 July 2010 Pages: 39 - 57
A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann–Sträussler–Scheinker disease phenotype: comparison with similar cases from the literature Casper JansenWillem VoetAnnemieke J. M. Rozemuller Original Paper Open access 03 March 2010 Pages: 59 - 68
Molecular pathology of human prion disease Jonathan D. F. WadsworthJohn Collinge Review Open access 08 August 2010 Pages: 69 - 77
Molecular biology and pathology of prion strains in sporadic human prion diseases Pierluigi GambettiIgnazio CaliWitold K. Surewicz Review 07 November 2010 Pages: 79 - 90
Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future Piero ParchiRosaria StrammielloHans Kretzschmar Review 24 November 2010 Pages: 91 - 112
Cellular and sub-cellular pathology of animal prion diseases: relationship between morphological changes, accumulation of abnormal prion protein and clinical disease Martin JeffreyGillian McGovernLorenzo González Review 08 June 2010 Pages: 113 - 134
The application of in vitro cell-free conversion systems to human prion diseases Michael JonesAlexander H. PedenJames W. Ironside Review 10 June 2010 Pages: 135 - 143