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Movement Disorders : Official Journal of the Movement Disorder Society|July 8, 2024
A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic DisorderTeije H van Prooije, Maartje Pennings, Lucille Dorresteijn, et al.Journal of Huntington'S Disease|April 26, 2024
Clinical Review of Juvenile Huntington's DiseaseMayke Oosterloo, Alexiane Touze, Lauren M Byrne, et al.Neurology. Clinical Practice|January 20, 2025
Improving the Clinical Diagnostic Criteria for Genetically Confirmed Adult-Onset Huntington Disease: Considering Nonmotor PresentationsCiaran M Considine, Clare M Eddy, Samuel A Frank, et al.European Journal of Human Genetics : EJHG|March 12, 2020
De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disabilityIris G M Wijnen, Hermine E Veenstra-Knol, Fleur Vansenne, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2026
Clinical, Genetic, and Imaging Characteristics of SCA27B: Insights from a Large Dutch CohortTeije H van Prooije, Maartje Pennings, Roderick P P W M Maas, et al.Pageof 4