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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp010c483n55h
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dc.contributor.advisorGould, Elizabeth-
dc.contributor.authorJia, Tim-
dc.date.accessioned2022-07-15T15:02:45Z-
dc.date.available2022-07-15T15:02:45Z-
dc.date.created2022-05-02-
dc.date.issued2022-07-15-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp010c483n55h-
dc.description.abstractMovement disorders such as Parkinson’s disease, essential tremor, and dystonia are incurable and can be resistant to pharmacological treatment. These and other neuropsychiatric disorders can significantly reduce quality of life and cause an economic burden. Deep-brain stimulation (DBS) has been shown to alleviate symptoms as an advanced therapeutic for some disease indications. Similarly, spinal cord stimulation (SCS) has been used for cases of chronic pain. However, the mechanisms of either are unclear. This narrative literature review aims to understand the mechanism behind DBS and SCS in order to evaluate potential synergies and future developments. Neurostimulation from DBS and SCS is suggested to regulate dysfunctional imbalances by modulating local and network activity and influencing glial cells. Developments and technological advances point towards targeted therapeutic interventions implementing optimized and adaptive closed-loop stimulation based on patient-specific neuroimaging and biomarkers. Future research can look into effects of multi-target stimulation, simultaneous use of DBS and SCS, and varying stimulation parameters.en_US
dc.format.mimetypeapplication/pdf
dc.language.isoenen_US
dc.titleStimulating the Brain and Spinal Cord: A Short-Circuit or the Future of Targeted Therapy?en_US
dc.typePrinceton University Senior Theses
pu.date.classyear2022en_US
pu.departmentNeuroscienceen_US
pu.pdf.coverpageSeniorThesisCoverPage
pu.contributor.authorid920146326
pu.certificateGlobal Health and Health Policy Programen_US
pu.mudd.walkinNoen_US
Appears in Collections:Neuroscience, 2017-2023
Global Health and Health Policy Program, 2017-2023

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