9 results match your criteria: "Stanford University Department of Neurology and Neurological Sciences[Affiliation]"
Res Sq
September 2023
Johns Hopkins Department of Anesthesiology and Critical Care Medicine: Johns Hopkins Medicine Department of Anesthesiology and Critical Care Medicine.
Background: Impaired cerebral autoregulation (CA) is one of several proposed mechanisms of acute brain injury in patients supported by extracorporeal membrane oxygenation (ECMO). The primary aim of this study was to determine the feasibility of continuous CA monitoring in adult ECMO patients. Our secondary aims were to describe changes in cerebral oximetry index (COx) and other metrics of CA over time and in relation to functional neurologic outcomes.
View Article and Find Full Text PDFFront Hum Neurosci
August 2023
Stanford University Department of Mechanical Engineering, Stanford, CA, United States.
Background: Prior work suggests that vibratory stimulation can reduce spasticity and hypertonia. It is unknown which of three predominant approaches (stimulation of the spastic muscle, antagonist muscle, or cutaneous regions) most reduces these symptoms.
Objective: Determine which vibrotactile stimulation approach is most effective at reducing spastic hypertonia among post-stroke patients.
ACS Chem Neurosci
July 2023
Stanford University Department of Radiology, Stanford, California 94305, United States.
Positron emission tomography (PET) is a powerful tool for studying neuroinflammatory diseases; however, current PET biomarkers of neuroinflammation possess significant limitations. We recently reported a promising dendrimer PET tracer ([F]OP-801), which is selectively taken up by reactive microglia and macrophages. Here, we describe further important characterization of [F]OP-801 in addition to optimization and validation of a two-step clinical radiosynthesis.
View Article and Find Full Text PDFClin Neurol Neurosurg
August 2022
Stanford University Department of Neurology and Neurological Sciences, Palo Alto, CA 94304, USA.
Objective: Electrical source localization (ESI) can help to identify the seizure onset zone or propagation zone, but it is unclear how dipole localization techniques influence surgical planning.
Methods: Patients who received a high density (HD)-EEG from 7/2014-7/2019 at Stanford were included if they met the following inclusion criteria: (1) adequate epileptiform discharges were recorded for source localization analysis, (2) underwent surgical treatment, which was at least 6 months before the survey. Interictal ESI was performed with the LORETA method on age matched MRIs.
Clin Park Relat Disord
January 2020
Cleveland Clinic Imaging Institute, 9500 Euclid Ave, Cleveland, OH 44195, United States of America.
Background And Purpose: The clinical diagnosis of progressive supranuclear palsy can be challenging, as the clinical presentation overlaps with that of Parkinson's disease and multiple system atrophy. We sought to examine the practical utility of radiologic markers of progressive supranuclear palsy by investigating whether these markers could distinguish between patients with progressive supranuclear palsy-Richardson syndrome (PSP-RS) and those with Parkinson's disease based on imaging obtained in a typical clinical setting, not in a prospective research environment.
Materials And Methods: This retrospective study included 13 patients with PSP-RS and 13 patients with Parkinson's disease who were followed for either condition at our institution at the time of the study and who had MRI records available.
Clin Neurophysiol
January 2020
Stanford University Department of Neurology and Neurological Sciences, Palo Alto, CA 94304, USA. Electronic address:
Objective: To assay EEG signal quality recorded with tripolar concentric ring electrodes (TCREs) compared to regular EEG electrodes.
Methods: EEG segments were recorded simultaneously by TCREs and regular electrodes, low-pass filtered at 35 Hz (REG35) and 70 Hz (REG70). Clips were rated blindly by nine electroencephalographers for presence or absence of key EEG features, relative to the "gold-standard" of the clinical report.
Mov Disord
January 2018
Stanford University Department of Neurology and Neurological Sciences, Stanford University School of Medicine, Stanford, California, USA.
Neurobiol Dis
December 2016
Stanford University Department of Neurology and Neurological Sciences, Rm H3136, SUMC, 300 Pasteur Drive, Stanford, CA 94305, USA; Stanford University Department of Neurosurgery, 300 Pasteur Drive, Stanford, CA 94305, USA.
Subthalamic nucleus (STN) local field potential (LFP) recordings demonstrate beta (13-30Hz) band oscillations in Parkinson's disease (PD) defined as elevations of spectral power. The amount of attenuation of beta band power on therapeutic levels of high frequency (HF) deep brain stimulation (DBS) and/or dopaminergic medication has been correlated with the degree of improvement in bradykinesia and rigidity from the therapy, which has led to the suggestion that elevated beta band power is a marker of PD motor disability. A fundamental question has not been answered: whether there is a prolonged attenuation of beta band power after withdrawal of chronic HF DBS and whether this is related to a lack of progression or even improvement in the underlying motor disability.
View Article and Find Full Text PDFIEEE Trans Neural Syst Rehabil Eng
September 2007
Stanford University Department of Neurology and Neurological Sciences, Division of Child Neurology, Stanford, CA 94305, USA.
For children who depend on devices to communicate, the rate of communication is a primary determinant of success. For children with motor impairments, the rate of communication may be limited by inability to contact buttons or cells rapidly or accurately. It is, therefore, essential to know how to adjust the device interface in order to maximize each child's rate of communication.
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