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Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|October 1, 2023
Spatial proteomics of hippocampal subfield-specific pathology in Alzheimer's disease and primary age-related tauopathyJamie M Walker, Miranda E Orr, Timothy C Orr, et al.Journal of Neuropathology and Experimental Neurology|January 24, 2023
The status of digital pathology and associated infrastructure within Alzheimer's Disease CentersRebeca Scalco, Yamah Hamsafar, Charles L White, et al.The American Journal of Pathology|June 27, 2007
TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusionsNigel J Cairns, Manuela Neumann, Eileen H Bigio, et al.Acta Neuropathologica Communications|February 15, 2022
Antemortem detection of Parkinson's disease pathology in peripheral biopsies using artificial intelligenceMaxim Signaevsky, Bahram Marami, Marcel Prastawa, et al.Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.Acta Neuropathologica|June 21, 2007
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar DegenerationNigel J Cairns, Eileen H Bigio, Ian R A Mackenzie, et al.Acta Neuropathologica|July 15, 2022
Distinct tau neuropathology and cellular profiles of an APOE3 Christchurch homozygote protected against autosomal dominant Alzheimer's dementiaDiego Sepulveda-Falla, Justin S Sanchez, Maria Camila Almeida, et al.Acta Neuropathologica Communications|August 6, 2021
Predictors of cognitive impairment in primary age-related tauopathy: an autopsy studyMegan A Iida, Kurt Farrell, Jamie M Walker, et al.Acta Neuropathologica|July 22, 2019
C9orf72 intermediate repeats are associated with corticobasal degeneration, increased C9orf72 expression and disruption of autophagyChristopher P Cali, Maribel Patino, Yee Kit Tai, et al.Genome Medicine|March 9, 2022
A neurodegenerative disease landscape of rare mutations in Colombia due to founder effectsJuliana Acosta-Uribe, David Aguillón, J Nicholas Cochran, et al.Pageof 16