MDS Abstracts

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

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Articles tagged "Eye movement"

  • 2019 International Congress

    Comparison of high versus low frequency subthalamic stimulation on eye movement

    MG. Ghilardi, L. Stock, C. Kruger-Zechlin, Z. Deeb, E. Fonoff, L. Timmermann, J. Waldthaler (Sao Paulo, Brazil)

    Objective: Compare the effects of subthalamic stimulation using high versus low frequency on saccadic and antisaccadic eye movements of idiopathic PD patients. Background: Parkinson’s disease…
  • 2019 International Congress

    GBA and ATP13A mutation and PD: clinical phenotype, eye movements and pathogenic implications

    GM. Riboldi, J. Martone, J. Rucker, JR. Rizzo, T. Hudson, W. Dauer, S. Frucht (New York, NY, USA)

    Objective: To characterize a patient with GBAand ATP13A2gene mutations. Background: Mutations of GBA(Glucocerebrosidase) and ATP13A2(P5-ATPase) genes are risk factors for Parkinson’s disease (PD). Homozygous mutations…
  • 2019 International Congress

    Use of directional stimulation to localize and troubleshoot STN-related contralateral gaze deviation: a case report

    C. Stahl, C. Cho, A. Mogilner, M. Pourfar (New York, NY, USA)

    Objective: To report a case in which STN stimulation-induced gaze deviation was mapped and managed using directional lead programming. Background: Deep Brain Stimulation (DBS) of…
  • 2019 International Congress

    A case of Aceruloplasminemia with vertical saccadic eye movement abnormalities

    O. Dogu, N. öksüz, H. Kaleagasi (Mersin, Turkey)

    Objective: We describe the phenotype, video-oculagraphic  and neuroradiological findings of a case of aceruloplasminemia (AC). Background: Aceruloplasminemia presents in adulthood and is characterized by microcytic…
  • 2019 International Congress

    Looking “cherry red spot myoclonus” in the eyes

    GM. Riboldi, J. Martone, JR. Rizzo, T. Hudson, S. Frucht, J. Rucker (New York, NY, USA)

    Objective: To describe eye movements in a cohort of patients affected with Sialidosis type 1. Background: Sialidosis, or Mucolipidosis type 1, is a rare autosomal…
  • 2018 International Congress

    Oculomotor Behavior in Healthy Caribbean: Does it reflect an increased vulnerability to degenerative Parkinsonism?

    A. Lannuzel, A. Lackmy, B. Tressières, R. Edragas, V. Pélonde-Erimée, C. Bonnet, S. Rivaud-Péchoux, E. Roze, B. Gaymard (Pointe-à-Pitre, Guadeloupe)

    Objective: To investigate the impact of environmental factors on eye movement performances in two populations composed of carefully selected healthy subjects with strikingly different ethnic…
  • 2018 International Congress

    Update on Convergence Spasm: Review of Psychogenic and Organic Case Reports

    R. Fekete, S. Jankovic (Valhalla, NY, USA)

    Objective: The aim is to evaluate case reports and series of convergence spasm (CS). Background: CS consists of episodes of convergence of the eyes, miosis,…
  • 2018 International Congress

    Using saccades as an early test of levodopa treatment in Parkinson’s Disease

    Z.J. Lu, S. Dillon, P. Zetegren, M. Brzezick, C. Kennard, J. FitzGerald, C. (Oxford, United Kingdom)

    Objective: It is important to know what potential confounding effects the medications used to treat Parkinson’s disease (PD) have on eye movement, in order to…
  • 2018 International Congress

    Eye tracking in patients with restless legs syndrome with and without augmentation – interim results of an ongoing study

    P. Ellmerer, B. Heim, M. Ritter, A. Stefani, E. Brandauer, E. Holzknecht, K. Seppi, B. Högl, W. Poewe, A. Djamshidian (Innsbruck, Austria)

    Objective: To assess the ability to inhibit eye movements towards a target by analysing antisaccades using an eye tracker. Background: Restless legs syndrome (RLS) is…
  • 2018 International Congress

    Study of eye movements by video-oculography in essential tremors

    M. De Verdal, A. Lozza, D. Renard, E. Thouvenot, G. Castelnovo (Nimes, France)

    Objective: To study eye movements by video-oculography (VOG) in ET patients, and to evaluate the possible relationship between oculomotor abnormalities and the hereditary character of…
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