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Clinical Biomechanics (Bristol, Avon)|July 10, 2023
Assessment of axial rotation movement in cervical dystonia using cone-beam computed tomographyJean-Pierre Bleton, Raphaël Portero, Kévin Zuber, et al.The Journal of Biological Chemistry|August 20, 2017
Region-specific protein misfolding cyclic amplification reproduces brain tropism of prion strainsNicolas Privat, Etienne Levavasseur, Serfildan Yildirim, et al.Frontiers in Genetics|October 17, 2019
Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to KnowMathias Schwartz, Jean-Philippe Brandel, Marie Lise Babonneau, et al.The Medical Journal of Australia|September 22, 2010
Iatrogenic Creutzfeldt-Jakob disease in Australia: time to amend infection control measures for pituitary hormone recipients?Alison Boyd, Genevieve M J A Klug, Lawrence B Schonberger, et al.Journal of Neuropathology and Experimental Neurology|July 17, 2009
Loss of cerebellar granule neurons is associated with punctate but not with large focal deposits of prion protein in Creutzfeldt-Jakob diseaseBaptiste A Faucheux, Nicolas Privat, Jean-Philippe Brandel, et al.Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|September 30, 2018
First European case of Creutzfeldt-Jakob disease with a PRNP G114V mutationLouis Cousyn, David Grabli, Danielle Seilhean, et al.International Journal of Epidemiology|May 1, 2002
Analysis of the geographical distribution of sporadic Creutzfeldt-Jakob disease in France between 1992 and 1998Jérôme Huillard D'Aignaux, Simon N Cousens, Nicole Delasnerie-Lauprêtre, et al.Nature Reviews. Neurology|May 11, 2021
The importance of ongoing international surveillance for Creutzfeldt-Jakob diseaseNeil Watson, Jean-Philippe Brandel, Alison Green, et al.Neuroscience Letters|October 13, 2006
V180I mutation of the prion protein gene associated with atypical PrPSc glycosylationStéphanie Chasseigneaux, Stéphane Haïk, Isabelle Laffont-Proust, et al.Plos One|July 31, 2008
Regulating factors of PrP glycosylation in Creutzfeldt-Jakob disease--implications for the dissemination and the diagnosis of human prion strainsEtienne Levavasseur, Isabelle Laffont-Proust, Emilie Morain, et al.Pageof 7