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Human Molecular Genetics|April 6, 2007
Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brainPeggy F Shelbourne, Christine Keller-McGandy, Wenya Linda Bi, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|December 17, 2009
Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysisRichard A Armstrong, William Ellis, Ronald L Hamilton, et al.
Brain Pathology (Zurich, Switzerland)|May 1, 2014
Huntington's disease (HD): degeneration of select nuclei, widespread occurrence of neuronal nuclear and axonal inclusions in the brainstemUdo Rüb, Matthias Hentschel, Katharina Stratmann, et al.
Human Molecular Genetics|March 26, 2002
Early phenotypes that presage late-onset neurodegenerative disease allow testing of modifiers in Hdh CAG knock-in miceVanessa C Wheeler, Claire-Anne Gutekunst, Vladimir Vrbanac, et al.
Movement Disorders Clinical Practice|October 3, 2017
Frequency of GBA variants in autopsy-proven multiple system atrophyMiriam Sklerov, Un Jung Kang, Christopher Liong, et al.
Neurobiology of Disease|December 11, 2012
Regional vulnerability in Huntington's disease: fMRI-guided molecular analysis in patients and a mouse model of diseaseNicole M Lewandowski, Yvette Bordelon, Adam M Brickman, et al.
Annals of Clinical and Translational Neurology|March 20, 2022
Correlation of plasma and neuroimaging biomarkers in Alzheimer's diseaseAdam M Brickman, Jennifer J Manly, Lawrence S Honig, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 23, 2023
Patterns of TDP-43 Deposition in Brains with LRRK2 G2019S MutationsJulian Agin-Liebes, Richard A Hickman, Jean Paul Vonsattel, et al.
Brain : a Journal of Neurology|September 12, 2014
A disease-specific metabolic brain network associated with corticobasal degenerationMartin Niethammer, Chris C Tang, Andrew Feigin, et al.
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