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Annals of Neurology|December 16, 2000
A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodiesM G Spillantini, H Yoshida, C Rizzini, et al.
The Journal of Comparative Neurology|November 22, 1989
Distribution of beta-nerve growth factor receptors in the human basal forebrainS J Allen, D Dawbarn, M G Spillantini, et al.
Annals of Neurology|October 17, 2001
Pick's disease associated with the novel Tau gene mutation K369IM Neumann, W Schulz-Schaeffer, R A Crowther, et al.
American Journal of Human Genetics|November 5, 1997
Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17J R Murrell, D Koller, T Foroud, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17L Varani, M Hasegawa, M G Spillantini, et al.
Dementia (Basel, Switzerland)|September 1, 1993
Phosphorylation of tau by cyclic-AMP-dependent protein kinaseJ Robertson, T L Loviny, M Goedert, et al.
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