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

Co-Occurrence of Types 1 and 2 PrP res in Sporadic Creutzfeldt-Jakob Disease MM1

(2011) Atsushi Kobayashi et al.   AMERICAN JOURNAL OF PATHOLOGY

A Second Case of Gerstmann-Sträussler-Scheinker Disease Linked to the G131V Mutation in the Prion Protein Gene in a Dutch Patient

(2011) Casper Jansen et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

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

(2010) Casper Jansen 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

Prospective 10-year surveillance of human prion diseases in Japan

(2010) I. Nozaki et al.   BRAIN

The first case of protease-sensitive prionopathy (PSPr) in The Netherlands: a patient with an unusual GSS-like clinical phenotype

(2010) C. Jansen et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau deposits

(2010) C. Jansen et al.   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

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

Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP

(2009) Casper Jansen et al.   ACTA NEUROPATHOLOGICA

Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt–Jakob disease brain reference materials

(2009) Helen M. Yull et al.   BIOLOGICALS

PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism

(2009) Matthew T Bishop et al.   BMC Medical Genetics

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

Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphology

(2009) C Jansen et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

A novel human disease with abnormal prion protein sensitive to protease

(2008) Pierluigi Gambetti et al.   ANNALS OF NEUROLOGY

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

Beyond PrPres Type 1/Type 2 Dichotomy in Creutzfeldt-Jakob Disease

(2008) Emmanuelle Uro-Coste et al.   PLoS Pathogens