MDS Abstracts

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

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Articles tagged "Eye movement"

  • 2019 International Congress

    Intact visuomotor forward models in adults with Tourette Syndrome

    A. Djodari-Irani, L. Kurvits, T. Mainka, A. Kühn, C. Ganos, F. Ostendorf (Berlin, Germany)

    Objective: To assess the integrity of forward model-driven predictions in a visuomotor task in adults with Tourette syndrome (TS). Background: Tics, such as those encountered…
  • 2019 International Congress

    Saccade profiles in Tourette syndrome

    Y. Sugiyama, H. Fukuda, Y. Terao, S. Tokushige, K. Hoshino, M. Hamada, Y. Ugawa, T. Toda (Tokyo, Japan)

    Objective: We investigated the performance of VGS and MGS to see whether the pathophysiology of TS represented the dopaminergic deficiency. Background: Tourette syndrome (TS) is…
  • 2019 International Congress

    Oculopalatal tremor (OPT) in a patient with anti-GAD brainstem encephalitis: A case report

    MF. Ip, SH. Li, TY. Wai, LY. Wong (Sheung Shui, Hong Kong)

    Objective: To report a case of OPT as consequence of anti-GAD brainstem encephalitis Background: OPT is caused by insult to the Guillain-Mollaret triangle. Common etiologies…
  • 2019 International Congress

    Study of eye movements as a tool in the diagnosis hereditary ataxias

    D. Gasca Saldaña, Y. Sánchez Jimenez, MC. Boll (Mexico City, Mexico)

    Objective: To study ocular movements (ocular pursuit, nystagmus and saccades) in the most frequent ataxias (SCA2, SCA3 and Friedreich's ataxia), to find out which variables…
  • 2019 International Congress

    Cognitive profile of degenerative parkinsonian syndromes in the French West Indies and relationship with eye movements recordings

    A. Petit, A. Lackmy, R. Edragas, S. Belson, A. Mongis-Marlin, C. Stattner, F. Triboulet, G. Lepage, B. Tressieres, B. Gaymard, A. Lannuzel (Fort de France, Martinique)

    Objective: To analyze the cognitive profile of patients with degenerative parkinsonian syndromes in the French West Indies and explore the correlations between cognitive deficits and…
  • 2019 International Congress

    Alcohol- Induced Cerebellar Ataxia

    B. Zeigelboim, H. Teive, C. Santos Junior, J. Malisky, M. da Rosa, R. Sampaio, M. José (Curitiba, Brazil)

    Objective: To verify vestibulocochlear disorders observed in a case of alcohol-induced cerebellar ataxia. Background: Alcohol-induced cerebellar degeneration is the commonest type of acquired toxic ataxia,…
  • 2019 International Congress

    Relationship between eye movements during natural reading and basic oculomotor tasks in PD

    J. Waldthaler, L. Stock, C. Krüger-Zechlin, L. Timmermann (Marburg, Germany)

    Objective: To investigate the relationship of eye movement characteristics during natural, self-paced reading and basic visually-guided saccades (VGS) and antisaccades (AS) tasks in PD. Background:…
  • 2019 International Congress

    Rare causes of Opsoclonus Myoclonus Ataxia Syndrome

    A. Venkitachalam, N. Chaudhary (Mumbai, India)

    Objective: To evaluate for rare causes of Opsoclonus Myoclonus Ataxia Syndrome. Background: Opsoclonus Myoclonus is a rare acute onset neurological disorder characterized by associated ocular,…
  • 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…
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