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Parkinsonism & Related Disorders|September 4, 2012
Parkinson's disease in patients and obligate carriers of Gaucher diseaseJoanna G Becker, Gregory M Pastores, Alessandro Di Rocco, et al.
Bioinformatics (Oxford, England)|February 15, 2026
From Genes to Trajectories: Mapping Genetic Influences on Huntington's Disease ProgressionSanjoy Dey, Zhaonan Sun, John Warner, et al.
Journal of the Neurological Sciences|December 1, 2009
Head trauma can initiate the onset of adreno-leukodystrophyGerald V Raymond, Roberta Seidman, Teshamae S Monteith, et al.
Journal of Inherited Metabolic Disease|February 24, 2010
The risk of Parkinson's disease in type 1 Gaucher diseaseGilberto Bultron, Katherine Kacena, Daniel Pearson, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 5, 2024
Time to Functional Loss as an Endpoint in Huntington's Disease Trials: Enrichment and Sample SizeJames A Mills, Jeffrey D Long, Jatin G Vaidya, et al.
Molecular Genetics and Metabolism|October 8, 2010
An open-label Phase I/II clinical trial of pyrimethamine for the treatment of patients affected with chronic GM2 gangliosidosis (Tay-Sachs or Sandhoff variants)Joe T R Clarke, Don J Mahuran, Swati Sathe, et al.
Frontiers in Neurology|September 6, 2021
Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's DiseaseSwati Sathe, Jen Ware, Jamie Levey, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 6, 2023
Defining Clinical Meaningfulness in Huntington's DiseaseJamie L Hamilton, James A Mills, Glenn T Stebbins, et al.
Blood Cells, Molecules & Diseases|November 12, 2010
The incidence of Parkinsonism in patients with type 1 Gaucher disease: data from the ICGG Gaucher RegistryBarry Rosenbloom, Manisha Balwani, Jeff M Bronstein, et al.
Journal of Huntington'S Disease|April 15, 2025
Functional Rating Scale 2.0 (FuRST 2.0): A patient-reported outcome measure of function for Huntington's diseaseRebecca Lm Fuller, Pua Feigenbaum, Nancy LaPelle, et al.
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