MDS Abstracts

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

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  • 2018 International Congress

    Comparative results between preoperative acute levodopa challenge test and deep brain stimulation

    D. Fitas, M.J. Rosas, J. Parada Lima, C. Reis, P. Linhares, R. Vaz (Viana do Castelo, Portugal)

    Objective: Our aim is to compare motor clinical benefits after acute levodopa challenge test, with those obtained further with deep brain stimulation (DBS). Background: DBS…
  • 2018 International Congress

    Deep brain stimulation for monogenic Parkinson’s disease: A systematic review

    T. Kuusimäki, J. Korpela, E. Pekkonen, M. Martikainen, A. Antonini, V. Kaasinen (Turku, Finland)

    Objective: The aim was to systematically investigate the outcome of deep brain stimulation (DBS) in genetic Parkinson’s disease (PD) compared to the patients with documented…
  • 2018 International Congress

    Long-term effect of low frequency stimulation of STN on dysphagia, freezing of gait and other motor symptoms in PD

    T. Xie, L. Bloom, M. Padmanaban, B. Bertacchi, W. Kang, A. Dachman, E. MacCracken, C. Zadikoff, K. Markopoulou, P. Warnke, U. Kang (Chicago, IL, USA)

    Objective: To evaluate the long-term effect of 60Hz low frequency stimulation (LFS) of the subthalamic nucleus (STN) on dysphagia, freezing of gait (FOG) and other…
  • 2018 International Congress

    Directional DBS; clinical experience at Unit of Functional Neurosurgery. Ramón y Cajal University Hospital,Madrid, Spain

    M. del Alamo, I. Martinez-Camacho, L. Cabañes, I. Regidor, M. Villadoniga, J. Garcia-de-la-Cruz, I. Avilés-Olmos (Madrid, Spain)

    Objective: to determine the practicabillity of using an image guide programming setting in our clinical practice. Background: The applicability of DBS leads and systems that…
  • 2018 International Congress

    Deep Brain Stimulation in Tourette Syndrome: Two illustrative cases

    X. Garcia, J. Espinoza, G. Arango (Bogota, Colombia)

    Objective: To describe two cases of patients with pharmacological refractory Tourette syndrome who underwent DBS in a single center in Bogota Colombia from 2012 -2015.…
  • 2018 International Congress

    Cerebrotendinous Xanthomatosis: A Rare Lipid Storage Disease

    H. Hanagasi, G. Yunisova, B. Bilgic, O. Dogu, H. Kaleagasi, Z. Tufekcioglu, E. Lohmann, H. Gurvit, M. Emre (Istanbul, Turkey)

    Objective: Cerebrotendinous xanthomatosis (CTX) is a rare autosomal recessive lipid storage disease. It is caused by the deficiency of mitochondrial enzyme sterol 27-hydroxylase due to…
  • 2018 International Congress

    Evaluation of Balance in Hereditary Ataxias

    H. Teive, B. Zeigelboim, R. Santos, S. Dias, N. Mello, V. Fonseca (Cuitiba, Brazil)

    Objective: To describe and compare the vestibular findings most evident among the hereditary ataxia, as well as correlate their clinical aspects to the study of…
  • 2018 International Congress

    Slowly progressive anti-Ca/ARHGAP26 autoantibody-associated cerebellar ataxia over 27 years without immunosuppressive treatment

    E. Schegk, I. Beiser, A. Wicki, L. Achtnichts, M. Bertschi (Aarau, Switzerland)

    Objective: To discuss a slowly progressive case of anti-Ca/ARHGAP26 autoantibody-associated cerebellar ataxia. Background: Anti-Ca/ARHGAP26 autoantibody-associated cerebellar ataxia was first identified in 2010 (1). Since then,…
  • 2018 International Congress

    Muscle Ultrasound Comparison Between Early And Intermediate Onset Friedreich’s Ataxia

    R. Verbeek, A. Waalkens, M. Kuiper, C. Verschuuren-Bemelmans, J. vd Hoeven, J. de Vries, J. van Gaalen, M. Willemsen, H. Kremer, D. Sival (Groningen, Netherlands)

    Objective: Background: Early-onset Friedreich’s Ataxia (FA) concerns a classic pediatric phenotype (p-FA, starting before 18 years of age), characterized by relentlessly progressive ataxia and (cardio)myopathy.…
  • 2018 International Congress

    Generalized dystonia and chorea with family history: Clinical case

    R. Varela, R. Araújo, M. Sousa, I. Alonso, A. Morgadinho, I. Fineza (Coimbra, Portugal)

    Objective: This clinical case intends to highlight the in expansion genotypic base of the genetically undefined benign hereditary chorea, where de adenylate cyclase 5 gene…
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