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Journal of Huntington'S Disease|July 27, 2014
The potential of composite cognitive scores for tracking progression in Huntington's diseaseRebecca Jones, Julie C Stout, Izelle Labuschagne, et al.Journal of Huntington'S Disease|October 8, 2015
Neuropsychiatry and White Matter Microstructure in Huntington's DiseaseSarah Gregory, Rachael I Scahill, Kiran K Seunarine, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 28, 2017
Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurementsAudrey Tanguy Melac, Caterina Mariotti, Antoine Filipovic Pierucci, et al.Neurology|December 19, 2025
Sequence Variants in Small CAG Repeat Expansions of the <i>HTT</i> Gene and Disease Onset and Progression in Huntington DiseaseAnna Heinzmann, Emilien Petit, Jessica Dawson, et al.Brain : a Journal of Neurology|August 16, 2023
Genetic topography and cortical cell loss in Huntington's disease link development and neurodegenerationCarlos Estevez-Fraga, Andre Altmann, Christopher S Parker, et al.Annals of Neurology|September 30, 2005
New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14Stephan Klebe, Alexandra Durr, Alexander Rentschler, et al.Neurology. Genetics|January 31, 2018
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 functionNatalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, et al.Journal of Medical Genetics|January 4, 2023
Fast and reliable detection of repeat expansions in spinocerebellar ataxia using exomesJean-Loup Méreaux, Claire-Sophie Davoine, Marie Coutelier, et al.Neurogenetics|July 31, 2007
Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab familiesNizar Elleuch, Naima Bouslam, Sylvain Hanein, et al.Brain and Behavior|March 14, 2023
Progressive alterations in white matter microstructure across the timecourse of Huntington's diseaseCarlos Estevez-Fraga, Michael S Elmalem, Marina Papoutsi, et al.Pageof 33