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Proceedings of the National Academy of Sciences of the United States of America|May 11, 2000
Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutationR Chiesa, B Drisaldi, E Quaglio, et al.
Journal of Experimental Psychology. Human Perception and Performance|February 1, 1979
Effects of S-R mapping and response modality on performance in a Stroop TaskJ R Simon, P Sudalaimuthu
Brain Research Bulletin|December 1, 1981
Purkinje cell loss and the noradrenergic system in the cerebellum of pcd mutant miceB Ghetti, R W Fuller, B D Sawyer, et al.
Archives of Virology. Supplementum|February 24, 2001
A transgenic model of a familial prion diseaseD A Harris, R Chiesa, B Drisaldi, et al.
Journal of the International Neuropsychological Society : JINS|March 1, 1997
Neuropsychological function in patients with Gerstmann-Sträussler-Scheinker disease from the Indiana kindred (F198S)F W Unverzagt, M R Farlow, J Norton, et al.
Journal of Medical Genetics|June 1, 1993
RFLP analysis for APP 717 mutations associated with Alzheimer's diseaseS R Zeldenrust, J Murrell, M Farlow, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1998
Mutation in the tau gene in familial multiple system tauopathy with presenile dementiaM G Spillantini, J R Murrell, M Goedert, et al.
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