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JAMA Neurology|May 24, 2013
Autoantibodies in sporadic Creutzfeldt-Jakob diseaseHeather Angus-Leppan, Peter Rudge, Simon Mead, et al.
Plos Genetics|February 14, 2009
HECTD2 is associated with susceptibility to mouse and human prion diseaseSarah E Lloyd, Emma G Maytham, Hirva Pota, et al.
BMC Neuroscience|March 25, 2014
Microglial Cx3cr1 knockout reduces prion disease incubation time in miceJulia Grizenkova, Shaheen Akhtar, Sebastian Brandner, et al.
International Psychogeriatrics|October 25, 2018
The most problematic symptoms of prion disease - an analysis of carer experiencesLiz Ford, Peter Rudge, Kathy Robinson, et al.
Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.
European Journal of Human Genetics : EJHG|June 26, 2022
Estimation of the number of inherited prion disease mutation carriers in the UKRosie Corbie, Tracy Campbell, Lee Darwent, et al.
Acta Neuropathologica|May 18, 2010
Tau, prions and Aβ: the triad of neurodegenerationLilla Reiniger, Ana Lukic, Jacqueline Linehan, et al.
Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
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