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Plos Currents|January 29, 2016
Medication Use in Early-HD Participants in Track-HD: an Investigation of its Effects on Clinical PerformanceRuth Keogh, Chris Frost, Gail Owen, et al.
Journal of Huntington'S Disease|January 13, 2016
Longitudinal Diffusion Tensor Imaging Shows Progressive Changes in White Matter in Huntington's DiseaseSarah Gregory, James H Cole, Ruth E Farmer, et al.
JAMA Neurology|July 12, 2016
Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic ApproachLouise-Laure Mariani, Christelle Tesson, Perrine Charles, et al.
Brain : a Journal of Neurology|September 20, 2015
Selective vulnerability of Rich Club brain regions is an organizational principle of structural connectivity loss in Huntington's diseasePeter McColgan, Kiran K Seunarine, Adeel Razi, et al.
The Lancet. Neurology|May 14, 2013
Predictors of phenotypic progression and disease onset in premanifest and early-stage Huntington's disease in the TRACK-HD study: analysis of 36-month observational dataSarah J Tabrizi, Rachael I Scahill, Gail Owen, et al.
JAMA Neurology|August 21, 2013
SYNE1 mutations in autosomal recessive cerebellar ataxiaAnne Noreau, Cynthia V Bourassa, Anna Szuto, et al.
Neurology|August 12, 2018
Nonataxia symptoms in Friedreich Ataxia: Report from the Registry of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS)Kathrin Reetz, Imis Dogan, Christian Hohenfeld, et al.
Biological Psychiatry|November 28, 2017
Brain Regions Showing White Matter Loss in Huntington's Disease Are Enriched for Synaptic and Metabolic GenesPeter McColgan, Sarah Gregory, Kiran K Seunarine, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 16, 2007
Spastic paraplegia 5: Locus refinement, candidate gene analysis and clinical descriptionStephan Klebe, Alexandra Durr, Naima Bouslam, et al.
Neuroimage. Clinical|July 24, 2018
Apathy and atrophy of subcortical brain structures in Huntington's disease: A two-year follow-up studyVerena Baake, Emma M Coppen, Erik van Duijn, et al.
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