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Human Molecular Genetics|May 13, 2005
Gene expression in Huntington's disease skeletal muscle: a potential biomarkerAndrew D Strand, Aaron K Aragaki, Dennis Shaw, et al.Movement Disorders Clinical Practice|April 5, 2021
Disease Onset in Huntington's Disease: When Is the Conversion?Mayke Oosterloo, Bianca T A de Greef, Emilia K Bijlsma, et al.Frontiers in Neurology|May 3, 2021
Validating Automated Segmentation Tools in the Assessment of Caudate Atrophy in Huntington's DiseaseNina M Mansoor, Tishok Vanniyasingam, Ian Malone, et al.Neuroimage|January 28, 2012
An event-based model for disease progression and its application in familial Alzheimer's disease and Huntington's diseaseHubert M Fonteijn, Marc Modat, Matthew J Clarkson, et al.Human Molecular Genetics|April 30, 2004
Somatic and germline mosaicism in sporadic early-onset Alzheimer's diseaseJonathan A Beck, Mark Poulter, Tracy A Campbell, et al.Neuroimage|June 16, 2009
Automated quantification of caudate atrophy by local registration of serial MRI: evaluation and application in Huntington's diseaseNicola Z Hobbs, Susie M D Henley, Edward J Wild, et al.Human Brain Mapping|October 11, 2015
Large-scale brain network abnormalities in Huntington's disease revealed by structural covarianceLora Minkova, Simon B Eickhoff, Ahmed Abdulkadir, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|January 13, 2026
Discovery of disrupted sustained attention and altered functional connectivity in far-from-onset Huntington's disease gene-expanded young adultsChristelle Langley, Michela Leocadi, Nicola Z Hobbs, et al.Plos One|December 23, 2017
Quantification of huntingtin protein species in Huntington's disease patient leukocytes using optimised electrochemiluminescence immunoassaysDavina J Hensman Moss, Nicola Robertson, Ruth Farmer, et al.Physical Therapy|July 12, 2014
Task-specific training in Huntington disease: a randomized controlled feasibility trialLori Quinn, Katy Debono, Helen Dawes, et al.Pageof 32