Showing results (31-40 of 350) with videos related to
Sort By:
Pageof 35
The American Journal of Psychiatry|March 4, 2014
Behavioral and psychiatric symptoms in prion diseaseAndrew Thompson, Angus MacKay, Peter Rudge, et al.Brain Communications|September 21, 2020
Enteral feeding is associated with longer survival in the advanced stages of prion diseaseKirsty McNiven, Akin Nihat, Tze How Mok, et al.Human Mutation|June 14, 2008
Successful amplification of degraded DNA for use with high-throughput SNP genotyping platformsSimon Mead, Mark Poulter, John Beck, et al.Scientific Reports|March 5, 2021
Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseasesTze How Mok, Akin Nihat, Connie Luk, et al.Plos One|January 26, 2013
Sod1 deficiency reduces incubation time in mouse models of prion diseaseShaheen Akhtar, Julia Grizenkova, Adam Wenborn, et al.Journal of Neurology|April 1, 2022
Assessing initial MRI reports for suspected CJD patientsAaron Jesuthasan, Danielle Sequeira, Harpreet Hyare, et al.Neurobiology of Aging|August 5, 2015
Inherited mtDNA variations are not strong risk factors in human prion diseaseGavin Hudson, James Uphill, Holger Hummerich, et al.JAMA Neurology|October 5, 2016
Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient UrineConnie Luk, Samantha Jones, Claire Thomas, 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.The Journal of General Virology|July 23, 2004
Characterization of two distinct prion strains derived from bovine spongiform encephalopathy transmissions to inbred miceSarah E Lloyd, Jacqueline M Linehan, Melanie Desbruslais, et al.Pageof 35