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Archives of Neurology|August 11, 2010
Heterozygosity at polymorphic codon 219 in variant creutzfeldt-jakob diseaseAna Lukic, Jonathan Beck, Susan Joiner, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New GuineaJohn Collinge, Jerome Whitfield, Edward McKintosh, et al.Brain : a Journal of Neurology|June 6, 2023
Clinical considerations in early-onset cerebral amyloid angiopathyGargi Banerjee, John Collinge, Nick C Fox, et al.Methods in Molecular Biology (Clifton, N.J.)|June 26, 2008
Molecular diagnosis of human prion diseaseJonathan D F Wadsworth, Caroline Powell, Jonathan A Beck, et al.Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|October 14, 2008
Review. Lessons of kuru research: background to recent studies with some personal reflectionsJohn CollingeNature|November 11, 2016
Mammalian prions and their wider relevance in neurodegenerative diseasesJohn CollingeJAMA Neurology|January 22, 2014
Variant Creutzfeldt-Jakob disease with extremely low lymphoreticular deposition of prion proteinSimon Mead, Jonathan D F Wadsworth, Marie-Claire Porter, et al.Human Molecular Genetics|May 17, 2014
In vitro screen of prion disease susceptibility genes using the scrapie cell assayCraig A Brown, Christian Schmidt, Mark Poulter, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 15, 2016
Quantitative EEG parameters correlate with the progression of human prion diseasesEdit Franko, Tim Wehner, Olivier Joly, et al.Proceedings of the National Academy of Sciences of the United States of America|June 30, 2026
A scalable, dividing cell model for the robust propagation and quantification of human sporadic Creutzfeldt-Jakob disease prionsAkin Nihat, Parineeta Arora, Christian Schmidt, et al.Pageof 43