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BMC Neurology|August 1, 2016
Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old manLaure Saint-Aubert, Jérémie Pariente, Herve Dumas, et al.Alzheimer Disease and Associated Disorders|October 1, 2011
Long-standing prion dementia manifesting as posterior cortical atrophyRaphaël Depaz, Stéphane Haik, Katell Peoc'h, et al.Acta Neuropathologica|December 7, 2017
Neuropathology of iatrogenic Creutzfeldt-Jakob disease and immunoassay of French cadaver-sourced growth hormone batches suggest possible transmission of tauopathy and long incubation periods for the transmission of Abeta pathologyCharles Duyckaerts, Véronique Sazdovitch, Kunie Ando, et al.The New England Journal of Medicine|August 8, 2014
Prions in the urine of patients with variant Creutzfeldt-Jakob diseaseFabio Moda, Pierluigi Gambetti, Silvio Notari, et al.Journal of Alzheimer'S Disease : JAD|March 31, 2012
Rapidly progressive Alzheimer's disease: a multicenter updateChristian Schmidt, Stephane Haïk, Katsuya Satoh, et al.Annals of Neurology|April 1, 2009
Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strainJean-Philippe Brandel, Craig A Heath, Mark W Head, et al.Emerging Infectious Diseases|September 29, 2012
Constant transmission properties of variant Creutzfeldt-Jakob disease in 5 countriesAbigail B Diack, Diane Ritchie, Matthew Bishop, et al.Science Translational Medicine|December 23, 2016
Detection of prions in the plasma of presymptomatic and symptomatic patients with variant Creutzfeldt-Jakob diseaseDaisy Bougard, Jean-Philippe Brandel, Maxime Bélondrade, et al.Plos One|March 26, 2013
Glycoform-selective prion formation in sporadic and familial forms of prion diseaseXiangzhu Xiao, Jue Yuan, Stéphane Haïk, et al.The Lancet. Neurology|February 20, 2021
Biomarkers and diagnostic guidelines for sporadic Creutzfeldt-Jakob diseasePeter Hermann, Brian Appleby, Jean-Philippe Brandel, et al.Pageof 7