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Movement Disorders : Official Journal of the Movement Disorder Society|February 27, 2009
Whole-brain atrophy as a measure of progression in premanifest and early Huntington's diseaseSusie M D Henley, Edward J Wild, Nicola Z Hobbs, et al.
Neurology. Genetics|October 18, 2021
Revealing the Timeline of Structural MRI Changes in Premanifest to Manifest Huntington DiseasePeter A Wijeratne, Sara Garbarino, Sarah Gregory, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 29, 2007
Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral bloodHeike Runne, Alexandre Kuhn, Edward J Wild, et al.
Frontiers in Neurology|October 26, 2017
Recommendations for the Use of Automated Gray Matter Segmentation Tools: Evidence from Huntington's DiseaseEileanoir B Johnson, Sarah Gregory, Hans J Johnson, et al.
Frontiers in Human Neuroscience|December 5, 2015
Detection of Motor Changes in Huntington's Disease Using Dynamic Causal ModelingLora Minkova, Elisa Scheller, Jessica Peter, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 13, 2010
Rate and acceleration of whole-brain atrophy in premanifest and early Huntington's diseaseEdward J Wild, Susie M D Henley, Nicola Z Hobbs, et al.
Journal of Huntington'S Disease|August 13, 2025
Bias in HD-ISS staging introduced by the FreeSurfer cross-sectional stream: Insights from the Huntington's Disease Young Adult Study (HD-YAS)Harry Knights, Annabelle Coleman, Mena Farag, et al.
Brain : a Journal of Neurology|June 20, 2019
MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1Michael Flower, Vilija Lomeikaite, Marc Ciosi, et al.
Neuroimage|May 6, 2014
Correction of inter-scanner and within-subject variance in structural MRI based automated diagnosingDaniel Kostro, Ahmed Abdulkadir, Alexandra Durr, et al.
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