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The American Journal of Pathology|December 1, 1994
Ultrastructure and biochemical composition of paired helical filaments in corticobasal degenerationH Ksiezak-Reding, K Morgan, L A Mattiace, et al.
Neurology|August 24, 2005
Survival in two variants of tau-negative frontotemporal lobar degeneration: FTLD-U vs FTLD-MNDK A Josephs, D S Knopman, J L Whitwell, et al.
Acta Neuropathologica|March 9, 2005
Extending the clinicopathological spectrum of neurofilament inclusion diseaseKeith A Josephs, Hirotake Uchikado, Rodney D McComb, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2017
Regional analysis and genetic association of nigrostriatal degeneration in Lewy body diseaseKoji Kasanuki, Michael G Heckman, Nancy N Diehl, et al.
Molecular Neurodegeneration|October 20, 2009
Development of monoclonal antibodies and quantitative ELISAs targeting insulin-degrading enzymeAnthony Delledonne, Naomi Kouri, Lael Reinstatler, et al.
Movement Disorders Clinical Practice|July 21, 2023
Perry Disease: Expanding the Genetic BasisJarosław Dulski, Shunsuke Koga, Paweł P Liberski, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 25, 2007
A presenilin 1 mutation (L420R) in a family with early onset Alzheimer disease, seizures and cotton wool plaques, but not spastic paraparesisAntony E Shrimpton, Robert L Schelper, Reinhold P Linke, et al.
Acta Neuropathologica|July 2, 2008
Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer diseaseWilliam T Hu, Keith A Josephs, David S Knopman, et al.
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