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Human Molecular Genetics|April 15, 2006
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's diseaseMaria Björkqvist, Asa Petersén, Karl Bacos, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 9, 2008
Huntington's disease phenocopies are clinically and genetically heterogeneousEdward J Wild, Ese E Mudanohwo, Mary G Sweeney, et al.Brain Communications|September 21, 2020
Activity or connectivity? A randomized controlled feasibility study evaluating neurofeedback training in Huntington's diseaseMarina Papoutsi, Joerg Magerkurth, Oliver Josephs, et al.Plos One|February 13, 2016
A Computational Cognitive Biomarker for Early-Stage Huntington's DiseaseThomas V Wiecki, Chrystalina A Antoniades, Alexander Stevenson, et al.Brain Communications|December 15, 2022
Intellectual enrichment and genetic modifiers of cognition and brain volume in Huntington's diseaseMarina Papoutsi, Michael Flower, Davina J Hensman Moss, et al.Human Molecular Genetics|October 26, 2018
FAN1 modifies Huntington's disease progression by stabilizing the expanded HTT CAG repeatRobert Goold, Michael Flower, Davina Hensman Moss, et al.Movement Disorders Clinical Practice|June 10, 2024
Outcomes of Percutaneous Endoscopic Gastrostomy in Huntington's Disease at a Tertiary CenterMena Farag, Annabelle Coleman, Harry Knights, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 6, 2012
Bone marrow transplantation confers modest benefits in mouse models of Huntington's diseaseWanda Kwan, Anna Magnusson, Austin Chou, et al.Journal of Huntington'S Disease|July 27, 2014
Reference genes selection for transcriptional profiling in blood of HD patients and R6/2 miceDaniela Diamanti, Nayana Lahiri, Alessia Tarditi, et al.BMC Biochemistry|November 27, 2013
Development of an ELISA assay for the quantification of soluble huntingtin in human blood cellsLuisa Massai, Lara Petricca, Letizia Magnoni, et al.Pageof 32