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Genetic research has identified several high- and variable-penetrance genes associated with Parkinson’s disease, including SNCA, PINK1, PRKN, and GBA.
Mitochondria play a critical role in Parkinson’s disease. Discover how mitochondrial dysfunction, oxidative stress, and genetic variations drive PD pathology.
Emerging evidence supports a strong link between immune system dysfunction, neuroinflammation, and the development of Parkinson’s disease.
The GBA1 gene plays a central role in cellular function and Parkinson’s disease pathogenesis. Explore how GBA1 mutations lead to dysfunction and neuroinflammation.
Protocol for a multi-arm, multi-stage platform trial, whereby patients are randomly assigned to one of four sub-studies and then further randomly assigned to receive active treatment or placebo. Such a protocol determines patient selection and outcome measures, incorporating biomarkers across the different sub-studies.
Brain drug delivery systems, allied with their characteristics for overcoming the blood-brain barrier (BBB).
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