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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.
Neurobiology of Aging|March 2, 2015
Rare structural genetic variation in human prion diseasesAna Lukic, James Uphill, Craig A Brown, et al.
Neurogenetics|December 17, 2002
Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in miceSarah E Lloyd, James B Uphill, Paul V Targonski, et al.
JAMA Neurology|March 30, 2026
High-Level Alzheimer Disease Neuropathological Change Following Iatrogenic ExposureGargi Banerjee, Tze How Mok, Harpreet Hyare, et al.
Genetics|August 22, 2008
Investigation of mcp1 as a quantitative trait gene for prion disease incubation time in mouseMarie O'Shea, Emma G Maytham, Jackie M Linehan, 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.
BMC Neurology|December 11, 2012
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob diseaseChristopher Carswell, Andrew Thompson, Ana Lukic, et al.
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