
Movement Disorders
Articles
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2 months ago |
acnr.co.uk | Movement Disorders |Parkinson’s Disease
Researchers from the Cleveland Clinic Genome Center have successfully applied advanced artificial intelligence (AI) genetics models to Parkinson’s disease. Researchers identified genetic factors in progression and FDA-approved drugs that can potentially be repurposed for PD treatment.
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Nov 27, 2024 |
academic.oup.com | Movement Disorders |Hayriye Cagnan
Essential tremor (ET) is one of the most common movement disorders in adults. Deep brain stimulation (DBS) of the ventralis intermediate nucleus (VIM) of the thalamus and/or the posterior subthalamic area (PSA) has been shown to provide significant tremor suppression in patients with ET, but with significant inter-patient variability and habituation to the stimulation.
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Jul 31, 2024 |
link.springer.com | Movement Disorders
AbstractFTLD-FET is a newly described subtype of frontotemporal lobar degeneration (FTLD characterized by pathologic inclusions of FET proteins: fused in sarcoma (FUS), Ewing sarcoma, and TATA-binding protein-associated factor 2N (TAF15)). Severe caudate volume loss on MRI has been linked to FTLD-FUS, yet glucose hypometabolism in FTLD-FET has not been studied. We assessed [18F] fluorodeoxyglucose PET (FDG-PET) hypometabolism in FTLD-FET subtypes and compared metabolism to FTLD-tau and FTLD-TDP.
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Jun 13, 2024 |
academic.oup.com | Movement Disorders
Control of actions allows adaptive, goal-directed behaviour. The basal ganglia, including the subthalamic nucleus, are thought to play a central role in dynamically controlling actions through recurrent negative feedback loops with the cerebral cortex. Here, we summarize recent translational studies that used deep brain stimulation to record neural activity from and apply electrical stimulation to the subthalamic nucleus in people with Parkinson’s disease.
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Jun 10, 2024 |
link.springer.com | Movement Disorders |Clinical Neuroscience
Parkinson’s disease (PD) diagnosis is based solely on clinical presentation [1]. Therefore, diagnostic and prognostic biomarkers are needed. In recent years, seeding aggregation assays (SAA) have demonstrated the ability to discriminate PD from controls, showing also potential as a predictive marker [2]. Furthermore, the development of modern proteomic techniques such as the proximity extension assay (PEA) has enabled high throughput, highly sensitive multiplexing studies to become more prevalent.
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