Advanced tests for early and accurate diagnosis of Creutzfeldt–Jakob disease

A Practical Approach to Avoiding Iatrogenic Creutzfeldt-Jakob Disease (CJD) from Invasive Instruments

(2015) Paul Brown et al.   INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY

Stability and Reproducibility Underscore Utility of RT-QuIC for Diagnosis of Creutzfeldt-Jakob Disease

(2015) Maria Cramm et al.   MOLECULAR NEUROBIOLOGY

A new prion disease: relationship with central and peripheral amyloidoses

(2015) Simon Mead et al.   Nature Reviews Neurology

Efficient propagation of variant Creutzfeldt-Jakob disease prion protein using the cell-protein misfolding cyclic amplification technique with samples containing plasma and heparin

(2015) Masatoshi Oshita et al.   TRANSFUSION

Bank Vole Prion Protein As an Apparently Universal Substrate for RT-QuIC-Based Detection and Discrimination of Prion Strains

(2015) Christina D. Orrú et al.   PLoS Pathogens

Olfactory bulb involvement in neurodegenerative diseases

(2014) Johannes Attems et al.   ACTA NEUROPATHOLOGICA

A highly specific blood test for vCJD

(2014) G. S. Jackson et al.   BLOOD

Characteristic CSF Prion Seeding Efficiency in Humans with Prion Diseases

(2014) Maria Cramm et al.   MOLECULAR NEUROBIOLOGY

A Test for Creutzfeldt–Jakob Disease Using Nasal Brushings

(2014) Christina D. Orrú et al.   NEW ENGLAND JOURNAL OF MEDICINE

Prions in the Urine of Patients with Variant Creutzfeldt–Jakob Disease

(2014) Fabio Moda et al.   NEW ENGLAND JOURNAL OF MEDICINE

Re-Assessment of PrPSc Distribution in Sporadic and Variant CJD

(2014) Richard Rubenstein et al.   PLoS One

Variant CJD

(2014) Abigail B Diack et al.   Prion

Detection of Misfolded Aβ Oligomers for Sensitive Biochemical Diagnosis of Alzheimer’s Disease

(2014) Natalia Salvadores et al.   Cell Reports

Preclinical Detection of Variant CJD and BSE Prions in Blood

(2014) Caroline Lacroux et al.   PLoS Pathogens

Prions and the Potential Transmissibility of Protein Misfolding Diseases

(2013) Allison Kraus et al.   Annual Review of Microbiology

Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob disease

(2013) Matthew T. Bishop et al.   BRAIN

A Novel Prion Disease Associated with Diarrhea and Autonomic Neuropathy

(2013) Simon Mead et al.   NEW ENGLAND JOURNAL OF MEDICINE

Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay

(2013) Kazunori Sano et al.   PLoS One

Prion protein and susceptibility to kainate-induced seizures

(2013) James F Striebel et al.   Prion

Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale survey

(2013) O. N. Gill et al.   BMJ-British Medical Journal

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

(2012) Piero Parchi et al.   ACTA NEUROPATHOLOGICA

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease

(2012) Lynne I. McGuire et al.   ANNALS OF NEUROLOGY

Differential Diagnosis of Jakob-Creutzfeldt Disease

(2012) Ross W. Paterson et al.   ARCHIVES OF NEUROLOGY

Sporadic human prion diseases: molecular insights and diagnosis

(2012) Gianfranco Puoti et al.   LANCET NEUROLOGY

Protein misfolding cyclic amplification of infectious prions

(2012) Rodrigo Morales et al.   Nature Protocols

Treatable neurological disorders misdiagnosed as Creutzfeldt-Jakob disease

(2011) Numthip Chitravas et al.   ANNALS OF NEUROLOGY

Allosteric function and dysfunction of the prion protein

(2011) Rafael Linden et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Cerebrospinal Fluid Markers in Sporadic Creutzfeldt-Jakob Disease

(2011) Gianluigi Zanusso et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assay

(2011) Julie Ann Edgeworth et al.   LANCET

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

(2011) Ryuichiro Atarashi et al.   NATURE MEDICINE

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias

(2011) P. Vitali et al.   NEUROLOGY

Prion Disease Blood Test Using Immunoprecipitation and Improved Quaking-Induced Conversion

(2011) C. D. Orru et al.   mBio

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

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

Variant CJD infection in the spleen of a neurologically asymptomatic UK adult patient with haemophilia

(2010) A. PEDEN et al.   HAEMOPHILIA

Protein aggregation diseases: pathogenicity and therapeutic perspectives

(2010) Adriano Aguzzi et al.   NATURE REVIEWS DRUG DISCOVERY

Strategies to reduce transfusion acquired vCJD

(2010) J. P. Wallis   TRANSFUSION MEDICINE

Rapid End-Point Quantitation of Prion Seeding Activity with Sensitivity Comparable to Bioassays

(2010) Jason M. Wilham et al.   PLoS Pathogens

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

(2009) I. Zerr et al.   BRAIN

Cellular prion protein mediates impairment of synaptic plasticity by amyloid-β oligomers

(2009) Juha Laurén et al.   NATURE

MRI lesion profiles in sporadic Creutzfeldt-Jakob disease

(2009) B. Meissner et al.   NEUROLOGY

A retrospective case note review of deceased recipients of vCJD-implicated blood transfusions

(2009) M. Gillies et al.   VOX SANGUINIS

Rapidly progressive dementia

(2008) Michael D. Geschwind et al.   ANNALS OF NEUROLOGY

Physiology of the Prion Protein

(2008) Rafael Linden et al.   PHYSIOLOGICAL REVIEWS