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Neuropathology and Applied Neurobiology|November 30, 2013
A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementiaTammaryn Lashley, Jonathan D Rohrer, Colin Mahoney, et al.Archives of Neurology|December 12, 2007
Creutzfeldt-Jakob disease, prion protein gene codon 129VV, and a novel PrPSc type in a young British womanSimon Mead, Susan Joiner, Melanie Desbruslais, et al.Brain Communications|August 17, 2022
Development of prognostic models for survival and care status in sporadic Creutzfeldt-Jakob diseaseAkın Nihat, Janice M Ranson, Dominique Harris, 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.Elife|August 7, 2024
Syntaxin-6 delays prion protein fibril formation and prolongs the presence of toxic aggregation intermediatesDaljit Sangar, Elizabeth Hill, Kezia Jack, et al.BMC Medical Genetics|April 9, 2016
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international studyRubika Balendra, James Uphill, Claire Collinson, 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.JAMA 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.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.Pageof 22