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Emerging Infectious Diseases|April 22, 2015
Recent US Case of Variant Creutzfeldt-Jakob Disease-Global ImplicationsAtul Maheshwari, Michael Fischer, Pierluigi Gambetti, et al.Neurobiology of Aging|March 2, 2021
A novel presenilin 1 duplication mutation (Ile168dup) causing Alzheimer's disease associated with myoclonus, seizures and pyramidal featuresAntoinette O'Connor, Emily Abel, M R Fraser, et al.Plos One|March 9, 2010
Genetic variability in CLU and its association with Alzheimer's diseaseRita J Guerreiro, John Beck, J Raphael Gibbs, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 15, 2018
Plasma tau is increased in frontotemporal dementiaMartha S Foiani, Ione Oc Woollacott, Carolin Heller, et al.Viruses|September 28, 2021
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat InsertionNicholas Brennecke, Ignazio Cali, Tze How Mok, et al.Nature|June 11, 2015
A naturally occurring variant of the human prion protein completely prevents prion diseaseEmmanuel A Asante, Michelle Smidak, Andrew Grimshaw, et al.BMJ (Clinical Research Ed.)|October 17, 2013
Prevalent abnormal prion protein in human appendixes after bovine spongiform encephalopathy epizootic: large scale surveyO Noel Gill, Yvonne Spencer, Angela Richard-Loendt, et al.Brain : a Journal of Neurology|May 28, 2011
Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factorsDiego N Kaski, Catherine Pennington, Jon Beck, et al.Molecular Psychiatry|March 6, 2021
Evaluation of plasma tau and neurofilament light chain biomarkers in a 12-year clinical cohort of human prion diseasesAndrew G B Thompson, Prodromos Anastasiadis, Ronald Druyeh, et al.Archives of Neurology|April 17, 2008
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin geneJonathan D Rohrer, Jason D Warren, Rohani Omar, et al.Pageof 22