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Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.Neurobiology of Disease|July 22, 2008
Hippocampal bursts caused by changes in NMDA receptor-dependent excitation in a mouse model of variant CJDStéphanie Ratté, Steven A Prescott, John Collinge, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Mortuary rites of the South Fore and kuruJerome T Whitfield, Wandagi H Pako, John Collinge, et al.Cell and Tissue Research|August 26, 2022
Prion strains viewed through the lens of cryo-EMSzymon W Manka, Adam Wenborn, John Collinge, et al.Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.Brain : a Journal of Neurology|February 28, 2012
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological featuresColin J Mahoney, Jon Beck, Jonathan D Rohrer, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 16, 2022
Iatrogenic cerebral amyloid angiopathy: an emerging clinical phenomenonGargi Banerjee, Kiran Samra, Matthew E Adams, et al.Brain Communications|September 21, 2020
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseasesHarpreet Hyare, Enrico De Vita, Marie-Claire Porter, et al.Pageof 36