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Cold Spring Harbor Perspectives in Medicine|October 30, 2016
Sporadic and Infectious Human Prion DiseasesRobert G Will, James W IronsideThe Journal of General Virology|September 12, 2006
Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob diseasePaula C Lourenco, Mary Jo Schmerr, Ian MacGregor, et al.Gene|May 30, 2002
PRNP contains both intronic and upstream regulatory regions that may influence susceptibility to Creutzfeldt-Jakob DiseaseJames E McCormack, Herbert N Baybutt, Dawn Everington, et al.Brain : a Journal of Neurology|March 2, 2013
Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt-Jakob diseaseMatthew T Bishop, Abigail B Diack, Diane L Ritchie, et al.Seminars in Hematology|December 24, 2003
The spectrum of safety: variant Creutzfeldt-Jakob disease in the United KingdomJames W IronsideComptes Rendus Biologies|February 28, 2002
Neuropathology of variant Creutzfeldt-Jakob diseaseJames W IronsidePrion|December 16, 2014
Variant CJD. 18 years of research and surveillanceAbigail B Diack, Mark W Head, Sandra McCutcheon, et al.AJNR. American Journal of Neuroradiology|September 19, 2003
Diagnosing variant Creutzfeldt-Jakob disease with the pulvinar sign: MR imaging findings in 86 neuropathologically confirmed casesDonald A Collie, David M Summers, Robin J Sellar, et al.Plos One|August 7, 2008
No major change in vCJD agent strain after secondary transmission via blood transfusionMatthew T Bishop, Diane L Ritchie, Robert G Will, et al.Pageof 19