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Journal of Neurology|November 14, 2008
Heightened incidence of sporadic Creutzfeldt-Jakob disease is associated with a shift in clinicopathological profilesKatharina Stoeck, Klaus Hess, Lorenz Amsler, et al.
Journal of Neurology|March 2, 2005
Sporadic Creutzfeldt-Jakob disease: a comparison of pathological findings and diffusion weighted imagingHeike Russmann, Francois Vingerhoets, Judith Miklossy, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 28, 2002
Unhampered prion neuroinvasion despite impaired fast axonal transport in transgenic mice overexpressing four-repeat tauValerie Künzi, Markus Glatzel, Michel Y Nakano, et al.
Plos Medicine|December 16, 2005
Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob diseaseGaby Schoch, Harald Seeger, Julien Bogousslavsky, et al.
Acta Neuropathologica|March 9, 2006
Cerebrovascular P-glycoprotein expression is decreased in Creutzfeldt-Jakob diseaseSilke Vogelgesang, Markus Glatzel, Lary C Walker, et al.
British Medical Bulletin|October 3, 2003
Immune system and peripheral nerves in propagation of prions to CNSAdriano Aguzzi, Frank L Heppner, Mathias Heikenwalder, et al.
The Journal of General Virology|May 26, 2005
No influence of amyloid-beta-degrading neprilysin activity on prion pathogenesisMarkus Glatzel, M Hasan Mohajeri, Raphael Poirier, et al.
Science (New York, N.Y.)|January 18, 2024
Prion science and its unsung heroesAdriano Aguzzi
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