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Movement Disorders : Official Journal of the Movement Disorder Society|September 26, 2025
Cerebrospinal Fluid Proenkephalin Predicts Striatal Atrophy Decades before Clinical Motor Diagnosis in Huntington's DiseaseMena Farag, Michael J Murphy, Nicola Z Hobbs, et al.Neurology|November 17, 2017
Motor, cognitive, and functional declines contribute to a single progressive factor in early HDScott A Schobel, Giuseppe Palermo, Peggy Auinger, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 1, 2009
Acid-sensing ion channel-1a in the amygdala, a novel therapeutic target in depression-related behaviorMatthew W Coryell, Amanda M Wunsch, Jill M Haenfler, et al.Journal of Huntington'S Disease|July 27, 2014
Corpus callosal atrophy in premanifest and early Huntington's diseaseHelen E Crawford, Nicola Z Hobbs, Ruth Keogh, et al.The Lancet. Neurology|December 6, 2011
Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational dataSarah J Tabrizi, Ralf Reilmann, Raymund A C Roos, et al.The Lancet. Neurology|December 7, 2010
Biological and clinical changes in premanifest and early stage Huntington's disease in the TRACK-HD study: the 12-month longitudinal analysisSarah J Tabrizi, Rachael I Scahill, Alexandra Durr, et al.Ebiomedicine|October 15, 2019
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomesMarc Ciosi, Alastair Maxwell, Sarah A Cumming, et al.Brain : a Journal of Neurology|December 1, 2023
Neurological disease in xeroderma pigmentosum: prospective cohort study of its features and progressionHector Garcia-Moreno, Douglas R Langbehn, Adesoji Abiona, et al.Nature Reviews. Neurology|March 12, 2014
Huntington disease: natural history, biomarkers and prospects for therapeuticsChristopher A Ross, Elizabeth H Aylward, Edward J Wild, et al.JAMA Neurology|August 13, 2019
Association of CAG Repeats With Long-term Progression in Huntington DiseaseDouglas R Langbehn, Julie C Stout, Sarah Gregory, et al.Pageof 9