Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

Human Prion Diseases in The Netherlands (1998–2009): Clinical, Genetic and Molecular Aspects

(2012) Casper Jansen et al.   PLoS One

National Institute on Aging–Alzheimer’s Association guidelines for the neuropathologic assessment of Alzheimer’s disease: a practical approach

(2011) Thomas J. Montine et al.   ACTA NEUROPATHOLOGICA

Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future

(2010) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

Genetic Creutzfeldt–Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis

(2010) Sabina Capellari et al.   ACTA NEUROPATHOLOGICA

Variably protease-sensitive prionopathy: A new sporadic disease of the prion protein

(2010) Wen-Quan Zou et al.   ANNALS OF NEUROLOGY

Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease

(2010) P. Parchi et al.   BRAIN

Experimental Verification of a Traceback Phenomenon in Prion Infection

(2010) A. Kobayashi et al.   JOURNAL OF VIROLOGY

Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties

(2010) M. T. Bishop et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrPSc types: an updated classification

(2009) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

Co-existence of scrapie prion protein types 1 and 2 in sporadic Creutzfeldt–Jakob disease: its effect on the phenotype and prion-type characteristics

(2009) Ignazio Cali et al.   BRAIN

Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients

(2008) Atsushi Kobayashi et al.   ACTA NEUROPATHOLOGICA

Inter-Laboratory Assessment of PrPScTyping in Creutzfeldt-Jakob Disease: A Western Blot Study within the NeuroPrion Consortium

(2008) Piero Parchi et al.   BRAIN PATHOLOGY

Characterization of Truncated Forms of Abnormal Prion Protein in Creutzfeldt-Jakob Disease

(2008) Silvio Notari et al.   JOURNAL OF BIOLOGICAL CHEMISTRY