Showing results (141-150 of 156) with videos related to

Sort By:
Pageof 16
Journal of Neuropathology and Experimental Neurology|June 8, 2017
Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG)Gabor G Kovacs, Sharon X Xie, Edward B Lee, et al.
Archives of Neurology|April 13, 2011
Genetic and clinical features of progranulin-associated frontotemporal lobar degenerationAlice S Chen-Plotkin, Maria Martinez-Lage, Patrick M A Sleiman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 23, 2022
Common Variants Near ZIC1 and ZIC4 in Autopsy-Confirmed Multiple System AtrophyFranziska Hopfner, Anja K Tietz, Viktoria C Ruf, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2024
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypesHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Acta Neuropathologica|December 15, 2015
Aging-related tau astrogliopathy (ARTAG): harmonized evaluation strategyGabor G Kovacs, Isidro Ferrer, Lea T Grinberg, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 8, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal CellsHui Wang, Timothy S Chang, Beth A Dombroski, et al.
Acta Neuropathologica|January 21, 2014
TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsMichael D Gallagher, Eunran Suh, Murray Grossman, et al.
Human Molecular Genetics|May 5, 2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseasesGiovanni Coppola, Subashchandrabose Chinnathambi, Jason JiYong Lee, et al.
Acta Neuropathologica|November 1, 2021
Genome-wide association study and functional validation implicates JADE1 in tauopathyKurt Farrell, SoongHo Kim, Natalia Han, et al.
Pageof 16