MDS Abstracts

Abstracts from the International Congress of Parkinson’s and Movement Disorders.

MENU 
  • Home
  • Meetings Archive
    • 2024 International Congress
    • 2023 International Congress
    • 2022 International Congress
    • MDS Virtual Congress 2021
    • MDS Virtual Congress 2020
    • 2019 International Congress
    • 2018 International Congress
    • 2017 International Congress
    • 2016 International Congress
  • Keyword Index
  • Resources
  • Advanced Search
  • MDS Virtual Congress 2020

    Neuronal Inclusion Formation and Axonal Degeneration in Mutant TFG Transgenic Mice

    T. Kawarai, A. Orlacchio, R. Kaji (Tokushima, Japan)

    Objective: To investigate the TFG pathology by analyzing transgenic mice expressing mutant TFG protein. Background: It has been demonstrated that missense variants in TFG gene…
  • MDS Virtual Congress 2020

    Evaluating patient out-of-pocket (OOP) expenses using real world utilization data of botulinum toxins

    L. Turner-Stokes, A. Lysandropoulos, S. Wietek, C. Divers (Harrow, United Kingdom)

    Objective: The objective of this study was to evaluate the impact of different brands of botulinum neurotoxin type A (BoNT-A) on OOP patient spending based…
  • MDS Virtual Congress 2020

    Treatment of Medication-Refectory Holmes Tremor by Simultaneous Thalamic Ventral Intermediate (VIM) Nucleus and Subthalamic Nucleus (STN) Deep Brain Stimulation-A Case Report

    M. Anjum, C. Kalhorn, Y. Torres-Yaghi, A. Carwin, F. Pagan (Washington, DC, USA)

    Objective: To report a case of medication refractory Holmes tremor in a patient with pontine stroke and multisystem atrophy-cerebellar type (MSA-C) successfully treated with bilateral,…
  • MDS Virtual Congress 2020

    A case report of myoclonus-dystonia with isolated myoclonus phenotype and novel mutation successfully treated with deep brain stimulation

    V. Besa Lehmann, M. Rosenbaum, L. Verhagen Metman (Santiago, Chile)

    Objective: Report the case of a patient with a novel SGCE gene mutation and isolated myoclonus phenotype who was successfully treated with deep brain stimulation…
  • MDS Virtual Congress 2020

    Intraparenchymal Cyst Formation and Spontaneous Regression following Deep Brain Stimulation Surgery

    A. Boddu, J. Siddiqui (Columbia, MO, USA)

    Objective: To present a case that highlights the recognition of a rare complication following deep brain stimulation (DBS) surgery and its management. Background: Deep brain…
  • MDS Virtual Congress 2020

    Thalamic deep brain stimulation improves tremor and spatio-temporal characteristics of gait in medically refractory orthostatic tremor

    A. Giritharan, M. Mancini, S. Stuart, R. Morris, S. Anderson, J. Wilhelm, J. Nutt (Portland, OR, USA)

    Objective: To characterize response to thalamic deep brain stimulation (DBS) in a patient with medically refractory orthostatic tremor using instrumented measures of tremor and mobility.…
  • MDS Virtual Congress 2020

    Non-Staged Bilateral GPi DBS Lead Revision Using iMRI: A Case Report

    B. Hwang, D. Mampre, K. Mills, A. Butala, W. Anderson (Baltimore, MD, USA)

    Objective: To demonstrate the feasibility of non-staged intraoperative MRI (iMRI) deep brain stimulation (DBS) lead revision under general anesthesia (GA). Background: DBS lead revision surgery…
  • MDS Virtual Congress 2020

    MRI guided high-intensity focused ultrasound thalamotomy for essential tremor: efficacy and safety at 1 year follow up

    V. Livneh, S. Israeli korn, G. Yahalom, T. Fay-Karmon, Z. Zibly, R. Spiegelmann, S. Baer (Ramat gan, Israel)

    Objective: To report our single-center experience with unilateral MRI guided high intensity focused ultrasound (MRgFUS) ventral intermediate nucleus (VIM) thalamotomy for patients with disabling essential tremor (ET). Background: ET causes functional disability, social isolationand psychological distress. Some patients are refractory…
  • MDS Virtual Congress 2020

    Bilateral GPi DBS for the treatment of severe generalized genetic dystonia caused by KMT2B mutation (DYT-28)

    J. Lopez-Castellanos, M. Lotia (Little Rock, AR, USA)

    Objective: . Background: KMT2B-related dystonia (DYT-28) is a complex childhood-onset movement disorder, characterized by a limb onset dystonia progressing to generalized dystonia with cranio-cervical involvement…
  • MDS Virtual Congress 2020

    Deep Brain Stimulation using Asymmetrical Targets in Rapid-onset Dystonia Parkinsonism (RDP)

    J.N Ong, J. Shin, H.J Kim, S.H Paek, B. Jeon (Seoul, Republic of Korea)

    Objective: We report our experience with deep brain stimulation (DBS) using asymmetrical targets in the right and left hemispheres for the treatment of dystonia in…
  • « Previous Page
  • 1
  • …
  • 676
  • 677
  • 678
  • 679
  • 680
  • …
  • 1554
  • Next Page »

Most Viewed Abstracts

  • This Week
  • This Month
  • All Time
  • Covid vaccine induced parkinsonism and cognitive dysfunction
  • Common mistakes in the MoCA test in patients with Parkinson’s Disease in Kyrgyzstan
  • Clinical Associations of Hand Deformities in Parkinson´s Disease
  • #24970 (not found)
  • Covid vaccine induced parkinsonism and cognitive dysfunction
  • What is the appropriate sleep position for Parkinson's disease patients with orthostatic hypotension in the morning?
  • Life expectancy with and without Parkinson’s disease in the general population
  • Effect of Ketone Ester Supplementation on Motor and Non-Motor symptoms in Parkinson's Disease
  • An atypical and interesting feature of Parkinson´s disease
  • Effect of marijuana on Essential Tremor: A case report
  • Increased Risks of Botulinum Toxin Injection in Patients with Hypermobility Ehlers Danlos Syndrome: A Case Series
  • Covid vaccine induced parkinsonism and cognitive dysfunction
  • Estimation of the 2020 Global Population of Parkinson’s Disease (PD)
  • Patients with Essential Tremor Live Longer than their Relatives
  • Help & Support
  • About Us
  • Cookies & Privacy
  • Wiley Job Network
  • Terms & Conditions
  • Advertisers & Agents
Copyright © 2025 International Parkinson and Movement Disorder Society. All Rights Reserved.
Wiley