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Parkinsonism & Related Disorders|June 22, 2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutationsChristina Sundal, Shinsuke Fujioka, Jay A Van Gerpen, et al.
Neurobiology of Aging|October 24, 2007
Prominent phenotypic variability associated with mutations in ProgranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Neurology|October 9, 2025
Core Clinical Features Associated With Survival in Patients With Dementia With Lewy BodiesStuart J McCarter, Tanis J Ferman, Kiera M Grant, et al.
Cell Reports|July 20, 2023
Poly(GR) interacts with key stress granule factors promoting its assembly into cytoplasmic inclusionsJinyoung Park, Yanwei Wu, Wei Shao, et al.
Parkinsonism & Related Disorders|July 5, 2016
MAPT haplotype diversity in multiple system atrophyCatherine Labbé, Michael G Heckman, Oswaldo Lorenzo-Betancor, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2026
TDP-43 subtypes shape transcriptomic signatures in Alzheimer's diseaseXiaojie Wang, Alyssa C Walker, Madison M Reeves, et al.
Annals of Clinical and Translational Neurology|March 22, 2018
Clinicopathological and 123I-FP-CIT SPECT correlations in patients with dementiaYoungsin Jung, Lennon G Jordan, Val J Lowe, et al.
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