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An update on best practice of deep brain stimulation in Parkinson’s disease
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inferredcites →https://doi.org/10.1001/archneur.61.1.89openalex-snapshot
Effects of High-Frequency Stimulation on Subthalamic Neuronal Activity in Parkinsonian Patients
inferredcites →https://doi.org/10.1001/archneur.62.4.554openalex-snapshot
Pallidal vs Subthalamic Nucleus Deep Brain Stimulation in Parkinson Disease
inferredcites →https://doi.org/10.1001/archneur.63.9.1273openalex-snapshot
Frequency-Dependent Reciprocal Modulation of Verbal Fluency and Motor Functions in Subthalamic Deep Brain Stimulation
inferredcites →https://doi.org/10.1001/archneurol.2010.260openalex-snapshot
Deep Brain Stimulation for Parkinson Disease
inferredcites →https://doi.org/10.1001/archneurol.2011.182openalex-snapshot
Ten-Year Outcome of Subthalamic Stimulation in Parkinson Disease
inferredcites →https://doi.org/10.1001/jama.2008.929openalex-snapshot
Bilateral Deep Brain Stimulation vs Best Medical Therapy for Patients With Advanced Parkinson Disease A Randomized Controlled Trial
inferredcites →https://doi.org/10.1001/jamaneurol.2014.1272openalex-snapshot
Effect of Advancing Age on Outcomes of Deep Brain Stimulation for Parkinson Disease
inferredcites →https://doi.org/10.1001/jamaneurol.2017.4321openalex-snapshot
Globus Pallidus Interna or Subthalamic Nucleus Deep Brain Stimulation for Parkinson Disease
inferredcites →https://doi.org/10.1002/acn3.168openalex-snapshot
Short pulse width widens the therapeutic window of subthalamic neurostimulation
inferredcites →https://doi.org/10.1002/ana.20091openalex-snapshot
Long‐term results of bilateral pallidal stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1002/ana.20402openalex-snapshot
Subthalamic stimulation activates internal pallidus: Evidence from cGMP microdialysis in PD patients
inferredcites →https://doi.org/10.1002/ana.21596openalex-snapshot
Cognition and mood in Parkinson's disease in subthalamic nucleus versus globus pallidus interna deep brain stimulation: The COMPARE Trial
inferredcites →https://doi.org/10.1002/ana.23951openalex-snapshot
Adaptive deep brain stimulation in advanced Parkinson disease
inferredcites →https://doi.org/10.1002/ana.410430208openalex-snapshot
Opposite motor effects of pallidal stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1002/hbm.23594openalex-snapshot
Toward an electrophysiological “sweet spot” for deep brain stimulation in the subthalamic nucleus
inferredcites →https://doi.org/10.1002/mdc3.12621openalex-snapshot
Multiple Microelectrode Recordings in STN‐DBS Surgery for Parkinson's Disease: A Randomized Study
inferredcites →https://doi.org/10.1002/mds.10162openalex-snapshot
Introduction to the programming of deep brain stimulators
inferredcites →https://doi.org/10.1002/mds.20135openalex-snapshot
The myth of microelectrode recording in ensuring a precise location of the DBS electrode within the sensorimotor part of the subthalamic nucleus
inferredcites →https://doi.org/10.1002/mds.20957openalex-snapshot
Deep brain stimulation: Postoperative issues
inferredcites →https://doi.org/10.1002/mds.20960openalex-snapshot
Electrophysiological mapping for the implantation of deep brain stimulators for Parkinson's disease and tremor
inferredcites →https://doi.org/10.1002/mds.20962openalex-snapshot
Subthalamic nucleus deep brain stimulation: Summary and meta-analysis of outcomes
inferredcites →https://doi.org/10.1002/mds.21481openalex-snapshot
Thirty days complication rate following surgery performed for deep‐brain‐stimulation
inferredcites →https://doi.org/10.1002/mds.22735openalex-snapshot
Long‐term results of a multicenter study on subthalamic and pallidal stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.22765openalex-snapshot
Comparison of weight gain and energy intake after subthalamic versus pallidal stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.25025openalex-snapshot
Short latency activation of cortex during clinically effective subthalamic deep brain stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.25535openalex-snapshot
Genotype and phenotype in Parkinson's disease: Lessons in heterogeneity from deep brain stimulation
inferredcites →https://doi.org/10.1002/mds.25610openalex-snapshot
Acute complications of movement disorders surgery: Effects of age and comorbidities
inferredcites →https://doi.org/10.1002/mds.26024openalex-snapshot
Subthalamic nucleus‐deep brain stimulation for early motor complications in Parkinson's disease—the EARLYSTIM trial: Early is not always better
inferredcites →https://doi.org/10.1002/mds.26080openalex-snapshot
Myths and facts about the EARLYSTIM study
inferredcites →https://doi.org/10.1002/mds.26292openalex-snapshot
Global cognitive scores do not predict outcome after subthalamic nucleus deep brain stimulation
inferredcites →https://doi.org/10.1002/mds.26827openalex-snapshot
Neuropsychological outcomes from constant current deep brain stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.27042openalex-snapshot
Pyramidal tract activation due to subthalamic deep brain stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1002/mds.27222openalex-snapshot
Quality of life outcome after subthalamic stimulation in Parkinson's disease depends on age
inferredcites →https://doi.org/10.1002/mds.27360openalex-snapshot
Disease Modification in Parkinson's Disease: Current Approaches, Challenges, and Future Considerations
inferredcites →https://doi.org/10.1007/s00415-005-0640-3openalex-snapshot
Deep brain stimulation in late stage Parkinson?s disease: a retrospective cost analysis in Germany
inferredcites →https://doi.org/10.1007/s00415-009-5121-7openalex-snapshot
Greater improvement in quality of life following unilateral deep brain stimulation surgery in the globus pallidus as compared to the subthalamic nucleus
inferredcites →https://doi.org/10.1007/s00415-014-7414-8openalex-snapshot
Subthalamic deep brain stimulation: clinical and neuropsychological outcomes in mild cognitive impaired parkinsonian patients
inferredcites →https://doi.org/10.1007/s00415-014-7605-3openalex-snapshot
Interleaved programming of subthalamic deep brain stimulation to avoid adverse effects and preserve motor benefit in Parkinson’s disease
inferredcites →https://doi.org/10.1007/s00415-016-8314-xopenalex-snapshot
Impulse control behaviors and subthalamic deep brain stimulation in Parkinson disease
inferredcites →https://doi.org/10.1007/s00701-005-0576-5openalex-snapshot
Hardware-related complications of deep brain stimulation: a ten year experience
inferredcites →https://doi.org/10.1007/s00701-007-1267-1openalex-snapshot
Complications in subthalamic nucleus stimulation surgery for treatment of Parkinson’s disease. Review of 272 procedures
inferredcites →https://doi.org/10.1007/s00701-010-0749-8openalex-snapshot
Surgical and hardware complications of deep brain stimulation. A seven-year experience and review of the literature
inferredcites →https://doi.org/10.1016/0006-8993(75)90364-9openalex-snapshot
Which elements are excited in electrical stimulation of mammalian central nervous system: A review
inferredcites →https://doi.org/10.1016/j.bbr.2012.11.038openalex-snapshot
Effects of 10Hz and 20Hz transcranial alternating current stimulation (tACS) on motor functions and motor cortical excitability
inferredcites →https://doi.org/10.1016/j.brs.2011.05.002openalex-snapshot
Current steering to activate targeted neural pathways during deep brain stimulation of the subthalamic region
inferredcites →https://doi.org/10.1016/j.brs.2011.07.001openalex-snapshot
Transient effects of 80 Hz stimulation on gait in STN DBS treated PD patients: A 15 months follow-up study
inferredcites →https://doi.org/10.1016/j.brs.2014.10.011openalex-snapshot
Low-frequency Versus High-frequency Subthalamic Nucleus Deep Brain Stimulation on Postural Control and Gait in Parkinson's Disease: A Quantitative Study
inferredcites →https://doi.org/10.1016/j.brs.2018.04.019openalex-snapshot
Less is more – Pulse width dependent therapeutic window in deep brain stimulation for essential tremor
inferredcites →https://doi.org/10.1016/j.brs.2018.05.005openalex-snapshot
Histopathology after microelectrode recording and twelve years of deep brain stimulation
inferredcites →https://doi.org/10.1016/j.clinph.2016.01.015openalex-snapshot
Subthalamic nucleus phase–amplitude coupling correlates with motor impairment in Parkinson’s disease
inferredcites →https://doi.org/10.1016/j.nbd.2015.10.009openalex-snapshot
A brain network model explaining tremor in Parkinson's disease
inferredcites →https://doi.org/10.1016/j.parkreldis.2006.01.004openalex-snapshot
Behavioural changes after bilateral subthalamic stimulation in advanced Parkinson disease: A systematic review
inferredcites →https://doi.org/10.1016/j.parkreldis.2010.05.003openalex-snapshot
Lessons learned from a large single center cohort of patients referred for DBS management
inferredcites →https://doi.org/10.1016/j.parkreldis.2010.12.005openalex-snapshot
Interleaving programming of subthalamic deep brain stimulation to reduce side effects with good motor outcome in a patient with Parkinson’s disease
inferredcites →https://doi.org/10.1016/j.parkreldis.2014.01.012openalex-snapshot
Long-term outcome of subthalamic nucleus DBS in Parkinson's disease: From the advanced phase towards the late stage of the disease?
inferredcites →https://doi.org/10.1016/j.parkreldis.2015.07.019openalex-snapshot
Long-term evaluation of impedance levels and clinical development in subthalamic deep brain stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1016/j.parkreldis.2016.09.014openalex-snapshot
An unexpectedly high rate of revisions and removals in deep brain stimulation surgery: Analysis of multiple databases
inferredcites →https://doi.org/10.1016/j.parkreldis.2016.09.018openalex-snapshot
Cognitive and psychiatric outcome 3 years after globus pallidus pars interna or subthalamic nucleus deep brain stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1016/j.wneu.2017.02.110openalex-snapshot
Deep Brain Stimulation of Pedunculopontine Nucleus for Postural Instability and Gait Disorder After Parkinson Disease: A Meta-Analysis of Individual Patient Data
inferredcites →https://doi.org/10.1016/s0079-6123(09)17525-8openalex-snapshot
Functional neurosurgery for movement disorders: a historical perspective
inferredcites →https://doi.org/10.1016/s0188-4409(00)00081-3openalex-snapshot
Vim Thalamic Stimulation for Tremor
inferredcites →https://doi.org/10.1016/s1015-9584(09)60404-8openalex-snapshot
Complications of Deep Brain Stimulation: A Collective Review
inferredcites →https://doi.org/10.1016/s1474-4422(09)70238-8openalex-snapshot
Neuropathological assessment of Parkinson's disease: refining the diagnostic criteria
inferredcites →https://doi.org/10.1016/s1474-4422(10)70093-4openalex-snapshot
Deep brain stimulation plus best medical therapy versus best medical therapy alone for advanced Parkinson's disease (PD SURG trial): a randomised, open-label trial
inferredcites →https://doi.org/10.1016/s1474-4422(12)70264-8openalex-snapshot
Subthalamic nucleus versus globus pallidus bilateral deep brain stimulation for advanced Parkinson's disease (NSTAPS study): a randomised controlled trial
inferredcites →https://doi.org/10.1016/s1474-4422(15)00087-3openalex-snapshot
Multiple-source current steering in subthalamic nucleus deep brain stimulation for Parkinson's disease (the VANTAGE study): a non-randomised, prospective, multicentre, open-label study
inferredcites →https://doi.org/10.1016/s1474-4422(18)30035-8openalex-snapshot
Behavioural outcomes of subthalamic stimulation and medical therapy versus medical therapy alone for Parkinson's disease with early motor complications (EARLYSTIM trial): secondary analysis of an open-label randomised trial
inferredcites →https://doi.org/10.1038/npjparkd.2016.24openalex-snapshot
The effect of deep brain stimulation on the non-motor symptoms of Parkinson’s disease: a critical review of the current evidence
inferredcites →https://doi.org/10.1038/nrneurol.2014.252openalex-snapshot
Axial disability and deep brain stimulation in patients with Parkinson disease
inferredcites →https://doi.org/10.1055/s-0032-1326957openalex-snapshot
Clinical Outcome of Subthalamic Stimulation in Parkinson's Disease is Improved by Intraoperative Multiple Trajectories Microelectrode Recording
inferredcites →https://doi.org/10.1056/nejmoa000827openalex-snapshot
Deep-Brain Stimulation of the Subthalamic Nucleus or the Pars Interna of the Globus Pallidus in Parkinson's Disease
inferredcites →https://doi.org/10.1056/nejmoa060281openalex-snapshot
A Randomized Trial of Deep-Brain Stimulation for Parkinson's Disease
inferredcites →https://doi.org/10.1056/nejmoa0907083openalex-snapshot
Pallidal versus Subthalamic Deep-Brain Stimulation for Parkinson's Disease
inferredcites →https://doi.org/10.1056/nejmoa1205158openalex-snapshot
Neurostimulation for Parkinson's Disease with Early Motor Complications
inferredcites →https://doi.org/10.1088/1741-2552/aad978openalex-snapshot
Clinical deep brain stimulation strategies for orientation-selective pathway activation
inferredcites →https://doi.org/10.1088/1741-2560/2/4/010openalex-snapshot
Current density distributions, field distributions and impedance analysis of segmented deep brain stimulation electrodes
inferredcites →https://doi.org/10.1093/brain/121.3.451openalex-snapshot
Subthalamic nucleus or internal pallidal stimulation in young onset Parkinson's disease
inferredcites →https://doi.org/10.1093/brain/awf050openalex-snapshot
Clinical predictive factors of subthalamic stimulation in Parkinson's disease
inferredcites →https://doi.org/10.1093/brain/awn214openalex-snapshot
A multicentre study on suicide outcomes following subthalamic stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1093/brain/awp229openalex-snapshot
Effects of pedunculopontine nucleus area stimulation on gait disorders in Parkinson's disease
inferredcites →https://doi.org/10.1093/brain/awp315openalex-snapshot
Reversing cognitive–motor impairments in Parkinson’s disease patients using a computational modelling approach to deep brain stimulation programming
inferredcites →https://doi.org/10.1093/brain/awq032openalex-snapshot
Non-motor dopamine withdrawal syndrome after surgery for Parkinson's disease: predictors and underlying mesolimbic denervation
inferredcites →https://doi.org/10.1093/brain/awq221openalex-snapshot
Motor and cognitive outcome in patients with Parkinson's disease 8 years after subthalamic implants
inferredcites →https://doi.org/10.1093/brain/awt122openalex-snapshot
Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial
inferredcites →https://doi.org/10.1093/brain/awt151openalex-snapshot
Relation of lead trajectory and electrode position to neuropsychological outcomes of subthalamic neurostimulation in Parkinson’s disease: results from a randomized trial
inferredcites →https://doi.org/10.1093/brain/awu102openalex-snapshot
Directional deep brain stimulation: an intraoperative double-blind pilot study
inferredcites →https://doi.org/10.1093/brain/aww223openalex-snapshot
Progressive gait ataxia following deep brain stimulation for essential tremor: adverse effect or lack of efficacy?
inferredcites →https://doi.org/10.1093/brain/aww286openalex-snapshot
Stimulating at the right time: phase-specific deep brain stimulation
inferredcites →https://doi.org/10.1093/brain/awx010openalex-snapshot
The modulatory effect of adaptive deep brain stimulation on beta bursts in Parkinson’s disease
inferredcites →https://doi.org/10.1097/00006123-199912000-00024openalex-snapshot
Comparison of Pallidal and Subthalamic Nucleus Deep Brain Stimulation for Advanced Parkinson's Disease: Results of a Randomized, Blinded Pilot Study
inferredcites →https://doi.org/10.1097/00006123-200008000-00005openalex-snapshot
Comparison of Anatomic and Neurophysiological Methods for Subthalamic Nucleus Targeting
inferredcites →https://doi.org/10.1097/00006123-200206000-00017openalex-snapshot
Long-term Hardware-related Complications of Deep Brain Stimulation
inferredcites →https://doi.org/10.1097/aco.0000000000000230openalex-snapshot
Anaesthesia for deep brain stimulation
inferredcites →https://doi.org/10.1101/cshperspect.a008862openalex-snapshot
The History of Parkinson's Disease: Early Clinical Descriptions and Neurological Therapies
inferredcites →https://doi.org/10.1111/ejn.14088openalex-snapshot
Mechanisms of action underlying the efficacy of deep brain stimulation of the subthalamic nucleus in Parkinson's disease: central role of disease severity
inferredcites →https://doi.org/10.1111/jnc.13649openalex-snapshot
Deep brain stimulation mechanisms: the control of network activity via neurochemistry modulation
inferredcites →https://doi.org/10.1111/ner.12227openalex-snapshot
The Rationale Driving the Evolution of Deep Brain Stimulation to Constant-Current Devices
inferredcites →https://doi.org/10.1111/ner.12397openalex-snapshot
Randomized, Blinded Pilot Testing of Nonconventional Stimulation Patterns and Shapes in Parkinson’s Disease and Essential Tremor: Evidence for Further Evaluating Narrow and Biphasic Pulses
inferredcites →https://doi.org/10.1111/ner.12553openalex-snapshot
Intraoperative Microstimulation Predicts Outcome of Postoperative Macrostimulation in Subthalamic Nucleus Deep Brain Stimulation for Parkinson’s Disease
inferredcites →https://doi.org/10.1111/ner.12740openalex-snapshot
Subthalamic Stimulation Improves Quality of Life of Patients Aged 61 Years or Older With Short Duration of Parkinson’s Disease
inferredcites →https://doi.org/10.1111/ner.12766openalex-snapshot
Comparison of Awake vs. Asleep Surgery for Subthalamic Deep Brain Stimulation in Parkinson’s Disease
inferredcites →https://doi.org/10.1126/science.1167093openalex-snapshot
Optical Deconstruction of Parkinsonian Neural Circuitry
inferredcites →https://doi.org/10.1136/jnnp-2012-304396openalex-snapshot
Suicide ideation and behaviours after STN and GPi DBS surgery for Parkinson’s disease: results from a randomised, controlled trial
inferredcites →https://doi.org/10.1136/jnnp-2014-310189openalex-snapshot
Postoperative apathy can neutralise benefits in quality of life after subthalamic stimulation for Parkinson's disease
inferredcites →https://doi.org/10.1136/jnnp.2008.159558openalex-snapshot
Brain penetration effects of microelectrodes and DBS leads in STN or GPi
inferredcites →https://doi.org/10.1152/jn.00989.2003openalex-snapshot
Cellular Effects of Deep Brain Stimulation: Model-Based Analysis of Activation and Inhibition
inferredcites →https://doi.org/10.1152/jn.2000.84.1.570openalex-snapshot
Microstimulation-Induced Inhibition of Neuronal Firing in Human Globus Pallidus
inferredcites →https://doi.org/10.1155/2016/6465793openalex-snapshot
Genetic Profile, Environmental Exposure, and Their Interaction in Parkinson’s Disease
inferredcites →https://doi.org/10.1155/2017/1939831openalex-snapshot
Are Patients Ready for “EARLYSTIM”? Attitudes towards Deep Brain Stimulation among Female and Male Patients with Moderately Advanced Parkinson’s Disease
inferredcites →https://doi.org/10.1159/000068960openalex-snapshot
Safety and Risk of Microelectrode Recording in Surgery for Movement Disorders
inferredcites →https://doi.org/10.1159/000100803openalex-snapshot
Combined (Thalamotomy and Stimulation) Stereotactic Surgery of the VIM Thalamic Nucleus for Bilateral Parkinson Disease
inferredcites →https://doi.org/10.1159/000475672openalex-snapshot
Accuracy of Intraoperative Computed Tomography during Deep Brain Stimulation Procedures: Comparison with Postoperative Magnetic Resonance Imaging
inferredcites →https://doi.org/10.1159/000478270openalex-snapshot
Deep Brain Stimulation for Tremor: Is There a Common Structure?
inferredcites →https://doi.org/10.1176/appi.neuropsych.10070109openalex-snapshot
Underlying Neurobiology and Clinical Correlates of Mania Status After Subthalamic Nucleus Deep Brain Stimulation in Parkinson's Disease: A Review of the Literature
inferredcites →https://doi.org/10.1212/01.wnl.0000144198.26309.d8openalex-snapshot
Subthalamic nucleus deep brain stimulation in Parkinson disease patients over age 70 years
inferredcites →https://doi.org/10.1212/01.wnl.0000234880.51322.16openalex-snapshot
Neurosurgery in Parkinson disease
inferredcites →https://doi.org/10.1212/01.wnl.0000260059.77107.c2openalex-snapshot
Is DBS-STN appropriate to treat severe Parkinson disease in an elderly population?
inferredcites →https://doi.org/10.1212/wnl.0000000000000943openalex-snapshot
Predicting quality of life outcomes after subthalamic nucleus deep brain stimulation
inferredcites →https://doi.org/10.1212/wnl.0000000000001419openalex-snapshot
Neuropsychological outcome after deep brain stimulation for Parkinson disease
inferredcites →https://doi.org/10.1212/wnl.0000000000002401openalex-snapshot
GPi vs STN deep brain stimulation for Parkinson disease
inferredcites →https://doi.org/10.1212/wnl.55.5.728openalex-snapshot
Failure of long-term pallidal stimulation corrected by subthalamic stimulation in PD
inferredcites →https://doi.org/10.1212/wnl.57.3.566-aopenalex-snapshot
Failure of long-term pallidal stimulation corrected by subthalamic stimulation in PD
inferredcites →https://doi.org/10.1227/00006123-199412000-00016openalex-snapshot
Bilateral Chronic Electrostimulation of Ventroposterolateral Pallidum
inferredcites →https://doi.org/10.1227/01.neu.0000289714.18297.41openalex-snapshot
REAL-TIME IMAGE GUIDANCE FOR OPEN VASCULAR NEUROSURGERY USING DIGITAL ANGIOGRAPHIC ROADMAPPING
inferredcites →https://doi.org/10.1227/01.neu.0000303993.82149.98openalex-snapshot
SINGLE ELECTRODE AND MULTIPLE ELECTRODE GUIDED ELECTRICAL STIMULATION OF THE SUBTHALAMIC NUCLEUS IN ADVANCED PARKINSON'S DISEASE
inferredcites →https://doi.org/10.1227/neu.0000000000000659openalex-snapshot
Adverse Events Associated With Deep Brain Stimulation for Movement Disorders
inferredcites →https://doi.org/10.1227/neu.0b013e3181f74105openalex-snapshot
An Assessment of Current Brain Targets for Deep Brain Stimulation Surgery With Susceptibility-Weighted Imaging at 7 Tesla
inferredcites →https://doi.org/10.1371/journal.pone.0114140openalex-snapshot
Acute and Chronic Mood and Apathy Outcomes from a Randomized Study of Unilateral STN and GPi DBS
inferredcites →https://doi.org/10.1371/journal.pone.0178984openalex-snapshot
Adverse events in deep brain stimulation: A retrospective long-term analysis of neurological, psychiatric and other occurrences
inferredcites →https://doi.org/10.1523/jneurosci.0275-12.2012openalex-snapshot
Beta Reactivity, Prospective Facilitation of Executive Processing, and Its Dependence on Dopaminergic Therapy in Parkinson's Disease
inferredcites →https://doi.org/10.1523/jneurosci.0360-05.2005openalex-snapshot
Pallidal Origin of GABA Release within the Substantia Nigra Pars Reticulata during High-Frequency Stimulation of the Subthalamic Nucleus
inferredcites →https://doi.org/10.1523/jneurosci.4144-11.2013openalex-snapshot
High-Frequency Pallidal Stimulation Disrupts Information Flow through the Pallidum by GABAergic Inhibition
inferredcites →https://doi.org/10.1586/17434440.2.4.409openalex-snapshot
Safety considerations for deep brain stimulation: review and analysis
inferredcites →https://doi.org/10.3109/02688697.2013.841859openalex-snapshot
Continuous perioperative apomorphine in deep brain stimulation surgery for Parkinson's disease
inferredcites →https://doi.org/10.3171/2012.8.jns112006openalex-snapshot
Effects of deep brain stimulation in the subthalamic nucleus or globus pallidus internus on step initiation in Parkinson disease
inferredcites →https://doi.org/10.3171/2013.8.focus13289openalex-snapshot
The added value of semimicroelectrode recording in deep brain stimulation of the subthalamic nucleus for Parkinson disease
inferredcites →https://doi.org/10.3171/2014.4.jns131711openalex-snapshot
Meta-analysis comparing deep brain stimulation of the globus pallidus and subthalamic nucleus to treat advanced Parkinson disease
inferredcites →https://doi.org/10.3171/2015.1.jns141604openalex-snapshot
“Rescue” of bilateral subthalamic stimulation by bilateral pallidal stimulation: case report
inferredcites →https://doi.org/10.3171/jns.2004.101.3.0511openalex-snapshot
Neurotransmitter release from high-frequency stimulation of the subthalamic nucleus
inferredcites →https://doi.org/10.3233/jpd-179007openalex-snapshot
My 25 Stimulating Years with DBS in Parkinson’s Disease
inferredcites →https://doi.org/10.3389/fncom.2016.00058openalex-snapshot
Model-Based Comparison of Deep Brain Stimulation Array Functionality with Varying Number of Radial Electrodes and Machine Learning Feature Sets
inferredcites →https://doi.org/10.3389/fneur.2018.00241openalex-snapshot
Outcomes of Interventional-MRI Versus Microelectrode Recording-Guided Subthalamic Deep Brain Stimulation
inferredcites →https://doi.org/10.3389/fnins.2014.00169openalex-snapshot
A neurochemical closed-loop controller for deep brain stimulation: toward individualized smart neuromodulation therapies
inferredcites →https://doi.org/10.3389/fnins.2015.00028openalex-snapshot
Quantitative analysis of axonal fiber activation evoked by deep brain stimulation via activation density heat maps
inferredcites →https://doi.org/10.3390/brainsci8010017openalex-snapshot
Awake versus Asleep Deep Brain Stimulation Surgery: Technical Considerations and Critical Review of the Literature
inferredcites →https://doi.org/10.4103/2152-7806.106265openalex-snapshot
Psychosis from subthalamic nucleus deep brain stimulator lesion effect
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3956658openalex-extracted
Persistent Relief of Motor Symptoms in a Parkinsonian Mouse Model After Induction of LTD at Cortical Inputs to Indirect Pathway Striatal Neurons
inferred← citeshttps://doi.org/10.1002/adfm.202105169openalex-snapshot
Advances in Triboelectric Nanogenerators for Self‐Powered Regenerative Medicine
inferred← citeshttps://doi.org/10.1002/advs.202401392openalex-snapshot
Gene Electrotransfer via Conductivity‐Clamped Electric Field Focusing Pivots Sensori‐Motor DNA Therapeutics: “A Spoonful of Sugar Helps the Medicine Go Down”
inferred← citeshttps://doi.org/10.1002/alz.13350openalex-snapshot
Sleep disorders in Lewy body dementia: Mechanisms, clinical relevance, and unanswered questions
inferred← citeshttps://doi.org/10.1002/ana.25994openalex-snapshot
Predictors of Long‐Term Outcome of Subthalamic Stimulation in Parkinson Disease
inferred← citeshttps://doi.org/10.1002/ana.78025openalex-snapshot
Beta Power Response After Levodopa Intake in Parkinson's Disease Patients With Chronic Sensing‐Enabled Deep Brain Stimulation
inferred← citeshttps://doi.org/10.1002/mdc3.13185openalex-snapshot
The Successful Three‐Year Outcome of Deep Brain Stimulation in Gaucher Disease Type 1 Associated Parkinson's Disease: A Case Report
inferred← citeshttps://doi.org/10.1002/mdc3.13660openalex-snapshot
Patients with Cognitive Impairment in Parkinson's Disease Benefit from Deep Brain Stimulation: A Case‐Control Study
inferred← citeshttps://doi.org/10.1002/mds.70042openalex-snapshot
Temporal Dynamics of Beta Power Related to the Stun Effect in Parkinson's Disease Patients after Deep Brain Stimulation Surgery
inferred← citeshttps://doi.org/10.1002/smll.202514955openalex-snapshot
Size Scaling of the Electrochemical Performance of Ti 3 C 2 T x MXene Microelectrode Arrays for Electrophysiological Recording and Stimulation
inferred← citeshttps://doi.org/10.1007/978-3-030-76469-2_11openalex-snapshot
Microelectrode Arrays, Implants, and Organs-on-a-Chip
inferred← citeshttps://doi.org/10.1007/978-3-031-40858-8_527-1openalex-snapshot
Neuromodulation for Movement Disorders
inferred← citeshttps://doi.org/10.1007/978-981-99-4538-2_7openalex-snapshot
Electrical Stimulation Techniques by Implantable Devices
inferred← citeshttps://doi.org/10.1007/s00221-023-06735-1openalex-snapshot
Unravelling the Parkinson’s puzzle, from medications and surgery to stem cells and genes: a comprehensive review of current and future management strategies
inferred← citeshttps://doi.org/10.1007/s00415-024-12751-0openalex-snapshot
Survey of common deep brain stimulation programming practices by experts in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s00455-020-10214-yopenalex-snapshot
The Effect of Deep Brain Stimulation on Swallowing Function in Parkinson’s Disease: A Narrative Review
inferred← citeshttps://doi.org/10.1007/s00481-025-00866-5openalex-snapshot
Die „soziale Kontraindikation“: Ein neurologischer Praxisbericht
inferred← citeshttps://doi.org/10.1007/s00702-019-02034-8openalex-snapshot
Dynamics of device-based treatments for Parkinson’s disease in Germany from 2010 to 2017: application of continuous subcutaneous apomorphine, levodopa–carbidopa intestinal gel, and deep brain stimulation
inferred← citeshttps://doi.org/10.1007/s00702-026-03106-2openalex-snapshot
Deep brain stimulation for Parkinson’s disease in India: an expert consensus on availability, affordability, and eligibility by the Parkinson’s research alliance India (PRAI)
inferred← citeshttps://doi.org/10.1007/s10072-023-06999-zopenalex-snapshot
Deep brain stimulation of globus pallidus internus and subthalamic nucleus in Parkinson’s disease: a multicenter, retrospective study of efficacy and safety
inferred← citeshttps://doi.org/10.1007/s10143-020-01429-6openalex-snapshot
Deep brain stimulation electrodes may rotate after implantation—an animal study
inferred← citeshttps://doi.org/10.1007/s10548-024-01054-2openalex-snapshot
Clinical and Brain Morphometry Predictors of Deep Brain Stimulation Outcome in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s10827-026-00954-5openalex-snapshot
Network state transitions under deep brain stimulation: A Wilson–Cowan model of Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s11406-021-00430-7openalex-snapshot
A Basic Nietzschean Model in Lieu of the Causal Maxim
inferred← citeshttps://doi.org/10.1007/s13205-023-03553-8openalex-snapshot
An update on pathogenesis and clinical scenario for Parkinson’s disease: diagnosis and treatment
inferred← citeshttps://doi.org/10.1007/s13311-023-01433-wopenalex-snapshot
Functional Brain Networks to Evaluate Treatment Responses in Parkinson's Disease
inferred← citeshttps://doi.org/10.1007/s13760-021-01778-zopenalex-snapshot
Cognitive outcome following bilateral subthalamic nucleus deep brain stimulation for Parkinson’s disease—a comparative observational study in Indian patients
inferred← citeshttps://doi.org/10.1007/s13760-026-03120-xopenalex-snapshot
Iranian Deep Brain Stimulation Registry for Parkinson’s Disease (IDBSR-PD): establishment and feasibility study
inferred← citeshttps://doi.org/10.1007/s40120-020-00220-5openalex-snapshot
Globus Pallidus Internus (GPi) Deep Brain Stimulation for Parkinson’s Disease: Expert Review and Commentary
inferred← citeshttps://doi.org/10.1007/s40592-020-00111-3openalex-snapshot
DBS: a compelling example for ethical and legal reflection—a French perspective on ethical and legal concerns about DBS
inferred← citeshttps://doi.org/10.1016/b978-0-323-91003-3.00005-2openalex-snapshot
Movement disorders and translational research
inferred← citeshttps://doi.org/10.1016/b978-0-323-95702-1.00212-8openalex-snapshot
Deep Brain Stimulation
inferred← citeshttps://doi.org/10.1016/b978-0-443-16128-5.00009-8openalex-snapshot
Deep brain stimulation using animal models of Parkinson's disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-18496-3.00019-7openalex-snapshot
Deep brain stimulation for depression
inferred← citeshttps://doi.org/10.1016/b978-0-443-36528-7.00028-5openalex-snapshot
Deep brain stimulation for movement disorders
inferred← citeshttps://doi.org/10.1016/bs.irmvd.2025.09.011openalex-snapshot
Right patient, right therapy: A regional perspective on device-aided treatments for Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.bbe.2021.04.016openalex-snapshot
Detection of subthalamic nucleus using novel higher-order spectra features in microelectrode recordings signals
inferred← citeshttps://doi.org/10.1016/j.bbe.2021.09.005openalex-snapshot
A novel deep recurrent convolutional neural network for subthalamic nucleus localization using local field potential signals
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.153858openalex-snapshot
40 Hz light flicker stimulation for neurodegenerative diseases: Mechanisms and clinical perspectives
inferred← citeshttps://doi.org/10.1016/j.brs.2020.09.024openalex-snapshot
Intraoperative changes in the H-reflex pathway during deep brain stimulation surgery for Parkinson’s disease: A potential biomarker for optimal electrode placement
inferred← citeshttps://doi.org/10.1016/j.brs.2021.09.002openalex-snapshot
Wearable sensor-driven responsive deep brain stimulation for essential tremor
inferred← citeshttps://doi.org/10.1016/j.brs.2022.07.048openalex-snapshot
Evoked potentials generated by deep brain stimulation for Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.brs.2023.07.002openalex-snapshot
Biomarker-guided neuromodulation aids memory in traumatic brain injury
inferred← citeshttps://doi.org/10.1016/j.brs.2024.01.006openalex-snapshot
Direct subthalamic nucleus stimulation influences speech and voice quality in Parkinson's disease patients
inferred← citeshttps://doi.org/10.1016/j.brs.2025.03.008openalex-snapshot
Subjective patient rating as a novel feedback signal for DBS programming in Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.brs.2025.04.019openalex-snapshot
Phase-dependent closed-loop deep brain stimulation of the fornix provides bidirectional manipulation of hippocampal theta oscillations
inferred← citeshttps://doi.org/10.1016/j.bspc.2026.109613openalex-snapshot
Intraoperative cognitive testing during deep brain stimulation surgery: A unique ethical method to obtain human task-electrophysiological data
inferred← citeshttps://doi.org/10.1016/j.clineuro.2026.109476openalex-snapshot
Underscore of geographical and referral barriers to deep brain stimulation treatment: A look at Parkinson’s and essential tremor patients in Western New York
inferred← citeshttps://doi.org/10.1016/j.clineuro.2026.109600openalex-snapshot
Postoperative outcomes in patients with dementia undergoing deep brain stimulation: A retrospective matched cohort study
inferred← citeshttps://doi.org/10.1016/j.compbiomed.2024.108465openalex-snapshot
Enhancing gait cadence through rhythm-modulated music: A study on healthy adults
inferred← citeshttps://doi.org/10.1016/j.cose.2021.102534openalex-snapshot
Neuronal Jamming cyberattack over invasive BCIs affecting the resolution of tasks requiring visual capabilities
inferred← citeshttps://doi.org/10.1016/j.expneurol.2024.114684openalex-snapshot
Insights into neuroinflammatory mechanisms of deep brain stimulation in Parkinson's disease
inferred← citeshttps://doi.org/10.1016/j.inat.2026.102298openalex-snapshot
Normative network-based programming for deep brain stimulation—Concept and case report
inferred← citeshttps://doi.org/10.1016/j.jdbs.2023.12.006openalex-snapshot
Microelectrode assisted deep brain stimulation: Considerations for anesthesia
inferred← citeshttps://doi.org/10.1016/j.jneumeth.2022.109687openalex-snapshot
Parkinson’s disease rodent models: Are they suitable for DBS research?
inferred← citeshttps://doi.org/10.1016/j.jocn.2024.03.033openalex-snapshot
Asleep versus awake GPi DBS surgery for Parkinson's disease: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.jpet.2025.103788openalex-snapshot
Striatal spinophilin enhances dopamine D2 receptor (D2R) interaction with cytosolic proteins to mediate persistent D2R agonist-induced locomotor suppression
inferred← citeshttps://doi.org/10.1016/j.jvoice.2023.09.027openalex-snapshot
Voice-Related Outcomes in Deep Brain Stimulation in Patients with Vocal Tremor: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.1016/j.nbd.2024.106698openalex-snapshot
Multiomics approach discloses lipids and metabolites profiles associated to Parkinson's disease stages and applied therapies
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.10.029openalex-snapshot
Structure-function similarities in deep brain stimulation targets cross-species
inferred← citeshttps://doi.org/10.1016/j.neucom.2025.131344openalex-snapshot
Neural cyberattacks applied to the vision under realistic visual stimuli
inferred← citeshttps://doi.org/10.1016/j.neuroimage.2026.121916openalex-snapshot
Treadmill exercise rebalances M1 response repertoires during motor state transitions in Parkinsonian mice
inferred← citeshttps://doi.org/10.1016/j.neurom.2022.09.008openalex-snapshot
Deep Brain Stimulation–Withdrawal Syndrome in Parkinson’s Disease: Risk Factors and Pathophysiological Hypotheses of a Life-Threatening Emergency
inferred← citeshttps://doi.org/10.1016/j.neuros.2025.100012openalex-snapshot
Exploring deep brain stimulation willingness in Black individuals with Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2021.02.019openalex-snapshot
Motor Thalamic Deep Brain Stimulation Alters Cortical Activity and Shows Therapeutic Utility for Treatment of Parkinson’s Disease Symptoms in a Rat Model
inferred← citeshttps://doi.org/10.1016/j.nicl.2021.102829openalex-snapshot
Variability in subthalamic nucleus targeting for deep brain stimulation with 3 and 7 Tesla magnetic resonance imaging
inferred← citeshttps://doi.org/10.1016/j.nicl.2023.103317openalex-snapshot
Alterations of resting-state networks of Parkinson‘s disease patients after subthalamic DBS surgery
inferred← citeshttps://doi.org/10.1016/j.parkreldis.2019.12.003openalex-snapshot
Deep brain stimulation for Parkinson disease – What does the short-term outcome analysis tell us?
inferred← citeshttps://doi.org/10.1016/j.parkreldis.2019.12.004openalex-snapshot
WITHDRAWN: Deep brain stimulation for Parkinson disease-What does the short-term outcome analysis tell us?
inferred← citeshttps://doi.org/10.1016/j.pnpbp.2026.111851openalex-snapshot
Deep brain stimulation and neuroimmune mechanisms in major depressive disorder
inferred← citeshttps://doi.org/10.1016/j.prdoa.2024.100273openalex-snapshot
Single-center experience of utilization and clinical efficacy of segmented leads for subthalamic deep brain stimulation in Parkinson’s disease
inferred← citeshttps://doi.org/10.1016/j.wneu.2023.06.079openalex-snapshot
Accuracy of Subthalamic Nucleus Electrode Implantation in Deep Brain Stimulation Surgery for Parkinson's Disease Treatment and Affecting Factors: Outcomes at Two Centers in Vietnam
inferred← citeshttps://doi.org/10.1016/j.wneu.2024.08.142openalex-snapshot
Incidental Brain Lesions in Parkinson Disease: High Prevalence, Minimal Impact on DBS Outcomes
inferred← citeshttps://doi.org/10.1017/cjn.2022.339openalex-snapshot
Emerging Neurotechnologies: Implications for Professional Relations and Communication
inferred← citeshttps://doi.org/10.1038/s41531-022-00403-xopenalex-snapshot
A systematic review of brain morphometry related to deep brain stimulation outcome in Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41531-023-00474-4openalex-snapshot
DBS-evoked cortical responses index optimal contact orientations and motor outcomes in Parkinson’s disease
inferred← citeshttps://doi.org/10.1038/s41598-025-07568-4openalex-snapshot
A bioelectric router for adaptive isochronous neurostimulation enables multipolar bioelectric stimulation from a single source
inferred← citeshttps://doi.org/10.1044/2024_jslhr-23-00511openalex-snapshot
Effects of Deep-Brain Stimulation on Speech: Perceptual and Acoustic Data
inferred← citeshttps://doi.org/10.1055/a-1046-0850openalex-snapshot
Tiefe Hirnstimulation bei Morbus Parkinson
inferred← citeshttps://doi.org/10.1055/a-1260-0401openalex-snapshot
Tiefe Hirnstimulation bei Morbus Parkinson
inferred← citeshttps://doi.org/10.1080/02688697.2025.2538488openalex-snapshot
YouTube videos for describing Deep Brain Stimulation: a comprehensive and quantitative review
inferred← citeshttps://doi.org/10.1080/17434440.2021.1962286openalex-snapshot
Deep brain stimulation programming strategies: segmented leads, independent current sources, and future technology
inferred← citeshttps://doi.org/10.1080/21646821.2025.2574104openalex-snapshot
Optimizing Outcomes: A Review of Pre- and Post-Surgical Evaluations in Deep Brain Stimulation for Parkinson’s Disease and Essential Tremor
inferred← citeshttps://doi.org/10.1088/1741-2552/ac1984openalex-snapshot
Thin-film microfabrication and intraoperative testing of µ ECoG and iEEG depth arrays for sense and stimulation
inferred← citeshttps://doi.org/10.1093/brain/awac184openalex-snapshot
Stimulation of the cuneiform nucleus enables training and boosts recovery after spinal cord injury
inferred← citeshttps://doi.org/10.1093/braincomms/fcae093openalex-snapshot
Insertional effect following electrode implantation: an underreported but important phenomenon
inferred← citeshttps://doi.org/10.1093/ons/opaa326openalex-snapshot
The Active Electrode in the Living Brain: The Response of the Brain Parenchyma to Chronically Implanted Deep Brain Stimulation Electrodes
inferred← citeshttps://doi.org/10.1097/md.0000000000038152openalex-snapshot
Deep brain stimulation in Parkinson’s disease: A scientometric and bibliometric analysis, trends, and research hotspots
inferred← citeshttps://doi.org/10.1101/2020.06.11.146886openalex-snapshot
Neural signatures of pathological hyperdirect pathway activity in Parkinson’s disease
inferred← citeshttps://doi.org/10.1101/2024.12.23.24319546openalex-snapshot
Long-term motor and cognitive outcome of Deep Brain Stimulation in GBA-PD: the Italian PARKNET study
inferred← citeshttps://doi.org/10.1101/2024.12.26.24319663openalex-snapshot
Quantitative Susceptibility Mapping Radiomics with Label Noise Compensation for Predicting Deep Brain Stimulation Outcomes in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1101/2025.01.28.635122openalex-snapshot
A Bioelectric Router for Adaptive Isochronous Neurostimulation
inferred← citeshttps://doi.org/10.1109/access.2022.3198980openalex-snapshot
Fabrication of a Flexible Three-Dimensional Hybrid Directional Lead for Deep Brain Stimulation and Control of Micturition Reflex in Rats
inferred← citeshttps://doi.org/10.1109/access.2025.3602824openalex-snapshot
Multipolar Stimulator for Deep Brain Stimulation With Suppression of Stimulation-Induced Common-Mode Artifacts
inferred← citeshttps://doi.org/10.1109/biocas58349.2023.10389168openalex-snapshot
Development of a magnetoelectric neural stimulator for in vitro experiments
inferred← citeshttps://doi.org/10.1109/jsen.2020.2988067openalex-snapshot
Dipole Fit Localization of the Deep Brain Stimulation Electrode Using 3D Magnetic Field Measurements
inferred← citeshttps://doi.org/10.1111/ejn.14898openalex-snapshot
Deep brain stimulation and eye movements
inferred← citeshttps://doi.org/10.1111/ner.13234openalex-snapshot
Directional Deep Brain Stimulation of the Thalamic Ventral Intermediate Area for Essential Tremor Increases Therapeutic Window
inferred← citeshttps://doi.org/10.1111/ner.13237openalex-snapshot
Asleep Surgery May Improve the Therapeutic Window for Deep Brain Stimulation of the Subthalamic Nucleus
inferred← citeshttps://doi.org/10.1136/bmjopen-2020-047670openalex-snapshot
Deep brain stimulation for locomotion in incomplete human spinal cord injury (DBS-SCI): protocol of a prospective one-armed multi-centre study
inferred← citeshttps://doi.org/10.1136/jnnp-2023-331248openalex-snapshot
Intraoperative physiology augments atlas-based data in awake deep brain stimulation
inferred← citeshttps://doi.org/10.1136/jnnp-2023-332387openalex-snapshot
Are patients with GBA–Parkinson disease good candidates for deep brain stimulation? A longitudinal multicentric study on a large Italian cohort
inferred← citeshttps://doi.org/10.1145/3535509openalex-snapshot
Eight Reasons to Prioritize Brain-Computer Interface Cybersecurity
inferred← citeshttps://doi.org/10.1145/3700666.3700702openalex-snapshot
A Multifunctional Software Platform developed in .net MAUI for performing Neural Stimulation with Low-Intensity Magnetic Fields
inferred← citeshttps://doi.org/10.1155/2020/8811435openalex-snapshot
Development and Initial Validation of the Chinese Version of the Florida Surgical Questionnaire for Parkinson’s Disease
inferred← citeshttps://doi.org/10.1155/2022/8132923openalex-snapshot
Reverse Visually Guided Reaching in Patients with Parkinson’s Disease
inferred← citeshttps://doi.org/10.1155/ijcp/7796155openalex-snapshot
The Promise and Pitfalls of Biomarkers for Differential Diagnosis in Parkinson’s Disease and Atypical Parkinsonism
inferred← citeshttps://doi.org/10.1159/000511424openalex-snapshot
A Phase 2 Randomized Trial of Asleep versus Awake Subthalamic Nucleus Deep Brain Stimulation for Parkinson’s Disease
inferred← citeshttps://doi.org/10.1159/000519960openalex-snapshot
Multicenter Validation of Individual Preoperative Motor Outcome Prediction for Deep Brain Stimulation in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1186/s12938-022-01062-yopenalex-snapshot
Neuro-nanotechnology: diagnostic and therapeutic nano-based strategies in applied neuroscience
inferred← citeshttps://doi.org/10.1186/s12984-025-01616-wopenalex-snapshot
Is physical therapy recommended for people with parkinson’s disease treated with subthalamic deep brain stimulation? a delphi consensus study
inferred← citeshttps://doi.org/10.1186/s41984-024-00281-wopenalex-snapshot
Subthalamic deep brain stimulation in advanced Parkinson’s disease using the STarFix system
inferred← citeshttps://doi.org/10.1212/wnl.0000000000214036openalex-snapshot
Long-Term Motor and Cognitive Outcome of Deep Brain Stimulation in Patients With Parkinson Disease With a GBA1 Pathogenic Variant
inferred← citeshttps://doi.org/10.1227/neu.0000000000003721openalex-snapshot
Technical Feasibility of Quantitative Susceptibility Mapping Radiomics for Predicting Deep Brain Stimulation Outcomes in Parkinson Disease
inferred← citeshttps://doi.org/10.1360/tb-2022-0338openalex-snapshot
Brain-computer interface—Brain information reading and activity control
inferred← citeshttps://doi.org/10.1364/boe.492552openalex-snapshot
Two-photon microendoscope for label-free imaging in stereotactic neurosurgery
inferred← citeshttps://doi.org/10.1371/journal.pmed.1004670openalex-snapshot
Deep brain stimulation surgical timing, outcomes, and prognostic factors in patients with Parkinson’s disease: A Chinese retrospective multicenter cohort study
inferred← citeshttps://doi.org/10.1371/journal.pone.0264114openalex-snapshot
Factors affecting postural instability after more than one-year bilateral subthalamic stimulation in Parkinson’s disease: A cross-sectional study
inferred← citeshttps://doi.org/10.1371/journal.pone.0275490openalex-snapshot
Automatic extraction of upper-limb kinematic activity using deep learning-based markerless tracking during deep brain stimulation implantation for Parkinson’s disease: A proof of concept study
inferred← citeshttps://doi.org/10.14802/jmd.20034openalex-snapshot
The Queensland Parkinson’s Project: An Overview of 20 Years of Mortality from Parkinson’s Disease
inferred← citeshttps://doi.org/10.1515/bmt-2020-0210openalex-snapshot
Therapeutic maps for a sensor-based evaluation of deep brain stimulation programming
inferred← citeshttps://doi.org/10.21307/ajon-2023-012openalex-snapshot
Understanding Parkinson's Disease: A Basic Overview
inferred← citeshttps://doi.org/10.2131/fts.7.253openalex-snapshot
Electromagnetic fields (EMF) facilitate cell migration and BrdU incorporation during an EMF-sensitive phase in a rat neurosphere assay in vitro
inferred← citeshttps://doi.org/10.2147/nss.s548093openalex-snapshot
Pathophysiological Insights and Multimodal Interventions in Chronic Tinnitus, Anxiety, and Sleep Disorders
inferred← citeshttps://doi.org/10.2174/011570159x446831260303200516openalex-snapshot
Molecular Mechanisms of Dopaminergic Neuron Degeneration in Parkinson’s Disease: A Comprehensive Review
inferred← citeshttps://doi.org/10.2174/9789815324846125010009openalex-snapshot
Intellectual Properties and Current Treatment Strategies for Targeting Neurodegenerative Disorders
inferred← citeshttps://doi.org/10.3171/2023.11.jns23882openalex-snapshot
Disparities in the treatment of movement disorders using deep brain stimulation
inferred← citeshttps://doi.org/10.3171/2024.4.jns24365openalex-snapshot
Radiographic abnormalities and their clinical significance in patients with Parkinson disease who receive deep brain stimulation implants
inferred← citeshttps://doi.org/10.3233/jpd-225101openalex-snapshot
Predicting Motor Outcome and Quality of Life After Subthalamic Deep Brain Stimulation for Parkinson’s Disease: The Role of Standard Screening Measures and Wearable-Data
inferred← citeshttps://doi.org/10.32598/jesm.11.2.7openalex-snapshot
Optimal Canceling of the Physiological Tremor for Rehabilitation in Parkinson’s Disease
inferred← citeshttps://doi.org/10.32776/revbiomed.v32i2.869openalex-snapshot
Estimulación cerebral profunda para la enfermedad de Parkinson: criterios de selección, abordaje quirúrgico, efectos secundarios y controversias.
inferred← citeshttps://doi.org/10.3389/fmedt.2024.1211585openalex-snapshot
Concept for intrathecal delivery of brain recording and stimulation device
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1534073openalex-snapshot
Recent advances (2022–2024) in eye-tracking for Parkinson’s disease: a promising tool for diagnosing and monitoring symptoms
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1734432openalex-snapshot
Effect of deep brain stimulation on dysphagia in Parkinson’s disease: mechanisms, evidence, and outlook
inferred← citeshttps://doi.org/10.3389/fneur.2022.1061274openalex-snapshot
Remote programming for subthalamic deep brain stimulation in Parkinson's disease
inferred← citeshttps://doi.org/10.3389/fneur.2022.980935openalex-snapshot
Encoding type, medication, and deep brain stimulation differentially affect memory-guided sequential reaching movements in Parkinson's disease
inferred← citeshttps://doi.org/10.3389/fneur.2023.1253241openalex-snapshot
Day one postoperative MRI findings following electrode placement for deep brain stimulation: analysis of a large case series
inferred← citeshttps://doi.org/10.3389/fnhum.2020.578216openalex-snapshot
The UF Deep Brain Stimulation Cognitive Rating Scale (DBS-CRS): Clinical Decision Making, Validity, and Outcomes
inferred← citeshttps://doi.org/10.3389/fnhum.2021.745689openalex-snapshot
Circuits for State-Dependent Modulation of Locomotion
inferred← citeshttps://doi.org/10.3389/fnhum.2022.1023917openalex-snapshot
Bilateral globus pallidus interna deep brain stimulation in Parkinson’s disease: Therapeutic effects and motor outcomes prediction in a short-term follow up
inferred← citeshttps://doi.org/10.3389/fnins.2021.670287openalex-snapshot
DeepNavNet: Automated Landmark Localization for Neuronavigation
inferred← citeshttps://doi.org/10.3389/fnins.2021.724334openalex-snapshot
Dopaminergic Modulation of Spectral and Spatial Characteristics of Parkinsonian Subthalamic Nucleus Beta Bursts
inferred← citeshttps://doi.org/10.3389/fnins.2021.734182openalex-snapshot
Patient, Caregiver, and Decliner Perspectives on Whether to Enroll in Adaptive Deep Brain Stimulation Research
inferred← citeshttps://doi.org/10.3389/fnins.2023.1282267openalex-snapshot
Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson’s disease and monogenic dystonia: a multidisciplinary team perspective
inferred← citeshttps://doi.org/10.3389/fresc.2026.1666530openalex-snapshot
Current status and future prospects of brain–computer interfaces in the field of neurological disease rehabilitation
inferred← citeshttps://doi.org/10.3390/biomedicines13112691openalex-snapshot
Deep Brain Stimulation: Mechanisms, Cost-Effectiveness, and Precision Applications Across Neurology and Psychiatry
inferred← citeshttps://doi.org/10.3390/brainsci14070638openalex-snapshot
New Perspectives of Deep Brain Stimulation Indications for Parkinson’s Disease: A Critical Review
inferred← citeshttps://doi.org/10.3390/genes17010069openalex-snapshot
Clinical Utility of GBA Genotyping Prior to Deep Brain Stimulation: A Narrative Review
inferred← citeshttps://doi.org/10.3390/ijms22126223openalex-snapshot
Bilirubin: A Promising Therapy for Parkinson’s Disease
inferred← citeshttps://doi.org/10.3390/ijms24076312openalex-snapshot
Effect of Electric Field on α-Synuclein Fibrils: Revealed by Molecular Dynamics Simulations
inferred← citeshttps://doi.org/10.3390/jcm9103124openalex-snapshot
Methodological Considerations for Neuroimaging in Deep Brain Stimulation of the Subthalamic Nucleus in Parkinson’s Disease Patients
inferred← citeshttps://doi.org/10.3390/s24061885openalex-snapshot
Principal Component Analysis Enhanced with Bootstrapped Confidence Interval for the Classification of Parkinsonian Patients Using Gaussian Mixture Model and Gait Initiation Parameters
inferred← citeshttps://doi.org/10.3390/s24196161openalex-snapshot
A Reconfigurable, Nonlinear, Low-Power, VCO-Based ADC for Neural Recording Applications
inferred← citeshttps://doi.org/10.3390/s25195999openalex-snapshot
A New Methodological Approach Integrating Motion Capture and Pressure-Sensitive Gait Data to Assess Functional Mobility in Parkinson’s Disease: A Two-Phase Study
inferred← citeshttps://doi.org/10.3390/s26051459openalex-snapshot
Continuous Accelerometry-Based Tremor Detection During Daily Living
inferred← citeshttps://doi.org/10.34024/rnc.2022.v30.11926openalex-snapshot
Trombólise venosa em paciente com Doença de Parkinson e DBS
inferred← citeshttps://doi.org/10.37990/medr.1330987openalex-snapshot
Association between Anesthesia Management and Preoperative Magnetic Resonance Image Quality in Patients Scheduled for Deep Brain Stimulation Surgery
inferred← citeshttps://doi.org/10.4018/979-8-3373-7437-6.ch007openalex-snapshot
Deep Brain Stimulation and Neuromodulation Advances for Parkinson's Disease
inferred← citeshttps://doi.org/10.47924/neurotarget2025546openalex-snapshot
Neuronal and Motor Activity in the Basal Ganglia During a Synchronization-Continuation Hand Tapping Task in Patients with Parkinson’s Disease
inferred← citeshttps://doi.org/10.48550/arxiv.2106.04968openalex-snapshot
Eight Reasons Why Cybersecurity on Novel Generations of Brain-Computer Interfaces Must Be Prioritized
inferred← citeshttps://doi.org/10.5334/tohm.712openalex-snapshot
Tremor in Parkinson’s Disease: From Pathophysiology to Advanced Therapies
inferred← citeshttps://doi.org/10.54101/acen.2022.2.10openalex-snapshot
Current understanding of neurostimulation for Parkinson's disease
inferred← citeshttps://doi.org/10.5772/intechopen.1006486openalex-snapshot
The Effects of Neurofeedback Training in Patients with Parkinson’s Disease
inferred← citeshttps://doi.org/10.5772/intechopen.110660openalex-snapshot
Principles of Rehabilitation Strategies in Spinal Cord Injury
inferred← citeshttps://doi.org/10.64898/2026.05.08.723848openalex-snapshot
Differentiating filter-induced oscillations from physiological stimulation-evoked potentials in intracranial recordings
inferred← citeshttps://doi.org/10.70675/48d08edbz6aafz427fza877zf5ee604b2a13openalex-snapshot
Optimisation du ciblage des noyaux gris centraux en neurochirurgie stéréotaxique
inferred← citeshttps://doi.org/10.70675/87e4f747zbcf8z45aaz8541z50965800f3c6openalex-snapshot
Role of synaptic zinc in pathophysiology of Parkinson’s disease
inferred← citeshttps://doi.org/10.70675/ebcaf07cz9890z4e15zb160z1746f591e65copenalex-snapshot
Bases neuro-fonctionnelles des troubles de l’impulsivité dans la maladie de Parkinson
inferred← citeshttps://doi.org/10.7759/cureus.76044openalex-snapshot
Comparison of Efficacy and Safety of Device-Based Interventions Versus Pharmacological Therapy in the Management of Patients With Advanced Parkinson’s Disease: A Literature Review
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