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Plos One|January 6, 2018
The language disorder of prion disease is characteristic of a dynamic aphasia and is rarely an isolated clinical featureDiana Caine, Akin Nihat, Philippa Crabb, et al.
BMC Neurology|June 29, 2021
Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob diseaseAhamad Hassan, Tracy Campbell, Lee Darwent, et al.
Brain : a Journal of Neurology|April 12, 2021
Cognitive decline heralds onset of symptomatic inherited prion diseaseJoseph Mole, Simon Mead, Peter Rudge, et al.
Scientific Reports|May 18, 2022
Prion protein gene mutation detection using long-read Nanopore sequencingFrançois Kroll, Athanasios Dimitriadis, Tracy Campbell, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2022
Prevalence and Treatments of Movement Disorders in Prion Diseases: A Longitudinal Cohort StudyDanielle Sequeira, Akin Nihat, Tzehow Mok, et al.
JAMA Neurology|March 30, 2026
High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic ExposureGargi Banerjee, Tze How Mok, Harpreet Hyare, et al.
Cancer Letters|December 4, 2018
Exosomes and cells from lung cancer pleural exudates transform LTC4 to LTD4, promoting cell migration and survival via CysLT1Ana Lukic, Casper J E Wahlund, Cristina Gómez, et al.
Annals of Indian Academy of Neurology|November 19, 2019
Familial Creutzfeldt-Jakob Disease in an Indian KindredSarosh M Katrak, Apoorva Pauranik, Shrinivas B Desai, et al.
Brain : a Journal of Neurology|January 31, 2019
Early neurophysiological biomarkers and spinal cord pathology in inherited prion diseasePeter Rudge, Zane Jaunmuktane, Harpreet Hyare, et al.
Lancet (London, England)|June 27, 2006
Kuru in the 21st century--an acquired human prion disease with very long incubation periodsJohn Collinge, Jerome Whitfield, Edward McKintosh, et al.
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