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Journal of Neurology|March 10, 2011
A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromesJonathan D Rohrer, Jason D Warren, David Reiman, et al.European Journal of Human Genetics : EJHG|April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experienceJane Owen, Jon Beck, Tracy Campbell, et al.JAMA Neurology|November 17, 2015
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological CorrelationLaura Eisenmenger, Marie-Claire Porter, Christopher J Carswell, et al.Cells|December 24, 2021
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease ProgressionDavid Mengel, Tze How Mok, Akin Nihat, et al.Methods in Molecular Biology (Clifton, N.J.)|September 2, 2017
Methods for Molecular Diagnosis of Human Prion DiseaseJonathan D F Wadsworth, Gary Adamson, Susan Joiner, et al.Nature Medicine|January 29, 2024
Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormoneGargi Banerjee, Simon F Farmer, Harpreet Hyare, et al.Lancet (London, England)|February 8, 2011
Detection of prion infection in variant Creutzfeldt-Jakob disease: a blood-based assayJulie Ann Edgeworth, Michael Farmer, Anita Sicilia, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Genetic susceptibility, evolution and the kuru epidemicSimon Mead, Jerome Whitfield, Mark Poulter, et al.Current Opinion in Neurology|November 16, 2004
Update on Creutzfeldt-Jakob diseaseGiovanna Mallucci, John CollingePageof 43