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Brain : a Journal of Neurology|September 29, 2019
Antemortem volume loss mirrors TDP-43 staging in older adults with non-frontotemporal lobar degenerationAlexandre Bejanin, Melissa E Murray, Peter Martin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2014
Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's diseaseKaren Nuytemans, Vanessa Inchausti, Gary W Beecham, et al.
Molecular Neurodegeneration|July 11, 2018
Replication of progressive supranuclear palsy genome-wide association study identifies SLCO1A2 and DUSP10 as new susceptibility lociMonica Y Sanchez-Contreras, Naomi Kouri, Casey N Cook, et al.
Neurology|September 29, 2020
Longitudinal anatomic, functional, and molecular characterization of Pick disease phenotypesJennifer L Whitwell, Nirubol Tosakulwong, Christopher C Schwarz, et al.
Brain Communications|April 25, 2024
Histologic tau lesions and magnetic resonance imaging biomarkers differ across two progressive supranuclear palsy variantsFrancesca Orlandi, Arenn F Carlos, Farwa Ali, et al.
The Journal of Clinical Investigation|February 26, 2026
Disruption of CSF-1 receptor-mediated metal ion homeostasis in the murine brain promotes neurodegenerative diseaseVioleta Chitu, Julia Alvarenga, Wenna Chen, et al.
Biorxiv : the Preprint Server for Biology|July 17, 2026
Targeted proteomics of postmortem human brain reveals neurobiologic heterogeneity in Alzheimer's disease using NULISA technologySara Rose Dunlop, Sarah J Lincoln, Zhongwei Peng, et al.
Neurology|February 11, 2021
Association of Mitochondrial DNA Genomic Variation With Risk of Pick DiseaseRebecca R Valentino, Michael G Heckman, Patrick W Johnson, et al.
Journal of Neuropathology and Experimental Neurology|May 8, 2007
The etiopathogenesis of Parkinson disease and suggestions for future research. Part IIIrene Litvan, Marie-Francoise Chesselet, Thomas Gasser, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|January 27, 2021
Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
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