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Archives of Neurology|September 16, 2009
Comparison of risk factor profiles in incidental Lewy body disease and Parkinson diseaseRoberta Frigerio, Hiroshige Fujishiro, Demetrius M Maraganore, et al.
Neuroscience Letters|July 4, 2009
GCH1 expression in human cerebellum from healthy individuals is not gender dependentChristian Wider, Sarah Lincoln, Justus C Dachsel, et al.
Neurobiology of Aging|April 17, 2012
Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlatesJennifer L Whitwell, Jia Xu, Jay Mandrekar, et al.
Brain : a Journal of Neurology|February 17, 2019
Selective loss of cortical endothelial tight junction proteins during Alzheimer's disease progressionYu Yamazaki, Mitsuru Shinohara, Motoko Shinohara, et al.
Brain : a Journal of Neurology|March 15, 2014
Regional distribution of synaptic markers and APP correlate with distinct clinicopathological features in sporadic and familial Alzheimer's diseaseMitsuru Shinohara, Shinsuke Fujioka, Melissa E Murray, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 14, 2012
Misregulation of human sortilin splicing leads to the generation of a nonfunctional progranulin receptorMercedes Prudencio, Karen R Jansen-West, Wing C Lee, et al.
Molecular Neurodegeneration|March 14, 2025
Probe-dependent Proximity Profiling (ProPPr) Uncovers Similarities and Differences in Phospho-Tau-Associated Proteomes Between TauopathiesDmytro Morderer, Melissa C Wren, Feilin Liu, et al.
Acta Neuropathologica Communications|August 30, 2020
Trans-synaptic and retrograde axonal spread of Lewy pathology following pre-formed fibril injection in an in vivo A53T alpha-synuclein mouse model of synucleinopathyAllison J Schaser, Teresa L Stackhouse, Leah J Weston, et al.
Parkinsonism & Related Disorders|December 13, 2012
TARDBP mutations in Parkinson's diseaseSruti Rayaprolu, Shinsuke Fujioka, Sharleen Traynor, et al.
Nature Communications|September 15, 2023
Divergent single cell transcriptome and epigenome alterations in ALS and FTD patients with C9orf72 mutationJunhao Li, Manoj K Jaiswal, Jo-Fan Chien, et al.
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