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Annals of Neurology|April 5, 2016
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseasesConceição Bettencourt, Davina Hensman-Moss, Michael Flower, et al.
The New England Journal of Medicine|May 7, 2019
Targeting Huntingtin Expression in Patients with Huntington's DiseaseSarah J Tabrizi, Blair R Leavitt, G Bernhard Landwehrmeyer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2021
An MDS Evidence-Based Review on Treatments for Huntington's DiseaseJoaquim J Ferreira, Filipe B Rodrigues, Gonçalo S Duarte, et al.
Nature Neuroscience|May 5, 2015
A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington diseaseKristina Bečanović, Anne Nørremølle, Scott J Neal, et al.
British Journal of Clinical Pharmacology|September 17, 2014
An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's diseaseSigurd D Süssmuth, Salman Haider, G Bernhard Landwehrmeyer, et al.
Journal of Huntington'S Disease|February 20, 2025
Study protocol for the iMarkHD study in individuals with Huntington's diseaseDaniel J van Wamelen, Naomi H Martin, Orsolya Makos, et al.
Scientific Reports|October 29, 2017
Myostatin inhibition prevents skeletal muscle pathophysiology in Huntington's disease miceMarie K Bondulich, Nelly Jolinon, Georgina F Osborne, et al.
Journal of Neurology|July 10, 2025
Evaluating finger-prick blood collection for remote quantification of neurofilament light in neurological diseasesAnnabelle Coleman, Alexiane Touzé, Mena Farag, et al.
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