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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.Journal of Alzheimer'S Disease : JAD|April 13, 2013
The presenilin 1 P264L mutation presenting as non-fluent/agrammatic primary progressive aphasiaColin J Mahoney, Laura E Downey, Jon 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.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.Expert Opinion on Biological Therapy|April 16, 2019
Facing the future: challenges and opportunities in adoptive T cell therapy in cancerIsabelle Magalhaes, Claudia Carvalho-Queiroz, Ciputra Adijaya Hartana, et al.Journal of Neurology|April 1, 2022
Assessing initial MRI reports for suspected CJD patientsAaron Jesuthasan, Danielle Sequeira, Harpreet Hyare, et al.The Lancet Regional Health. Europe|December 30, 2025
Estimating future variant Creutzfeldt-Jakob disease cases in the UK: a cohort-based probabilistic modelBarnaby Roberts, James Riley, Thomas J Evans, 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.Acta Neuropathologica|February 17, 2018
Evidence of amyloid-β cerebral amyloid angiopathy transmission through neurosurgeryZane Jaunmuktane, Annelies Quaegebeur, Ricardo Taipa, 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.Pageof 22