MDS Abstracts

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

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  • 2018 International Congress

    Biofabricated tissue constructs to recapitulate the anatomy and functionality of the nigrostriatal pathway in Parkinson’s disease

    J. Duda, L. Struzyna, K. Browne, H. Chen, D. Cullen (Philadelphia, PA, USA)

    Objective: 1) Biofabricate constructs that mimic the cytoarchitecture and function of the nigrostriatal pathway, and 2) Microinject constructs to assess restoration of dopaminergic input to…
  • 2018 International Congress

    Bilateral stereotypy after unilateral cerebellar infarction

    S. Choi, C. Shin, T. Ahn (Seoul, Republic of Korea)

    Objective: To report a case with bilateral hand stereotypy after left cerebellar infarction Background: Stereotypy is defined as repetitive and continuous non-goal-directed movement. It was…
  • 2018 International Congress

    Motor cortical excitability during voluntary inhibition of involuntary tic movements

    C. Ganos, L. Rocchi, A. Latorre, L. Hockney, C. Palmer, E. Joyce, K. Bhatia, P. Haggard, J. Rothwell (Berlin, Germany)

    Objective: To explore state-dependent effects of voluntary tic inhibition on M1 excitability. Background: Tics can be voluntarily inhibited. However, the neurophysiology of voluntary tic inhibition…
  • 2018 International Congress

    Alterations of the intestinal microbiota were correlated with the severity of Tourette syndrome in children

    WT. Lee, LC. Wong (Taipei, Taiwan)

    Objective: The current study aims to investigate the role and change of gut microbiota in children with Tourette syndrome (TS). Background: Tourette syndrome (TS) is…
  • 2018 International Congress

    Clinical and morphometric features of the tics

    S. Munasipova, Z. Zalyalova (Kazan, Russian Federation)

    Objective: To evaluate clinical and morphometric features in patients with tics in association with OCD and ADHD Background: In recent years there have been reports…
  • 2018 International Congress

    A case report of an Egyptian family with a rare condition of choreoacanthocytosis and amyotrophy

    A. Dahshan, S. Ahmed, A. Hasan, A.S. Othman, D. Mekkawy, O. Yakoub, D. Abdulatif, Y. Gamil (Cairo, Egypt)

    Objective: This reports an Egyptian family with two members with the rare condition of choreoacanthocytosis and amyotrophy. Background: choreoacanthocytosis is an autosomal recessive disorder caused…
  • 2018 International Congress

    Imaging Analysis of the International Tourette Syndrome Deep Brain Stimulation Registry and Database

    K. Johnson, D. Servello, M. Porta, A. Bona, J. Ostrem, E. Bardinet, ML. Welter, A. Lozano, J.C. Baldermann, J. Kuhn, D. Huys, T. Foltynie, M. Hariz, E. Joyce, L. Zrinzo, Z. Kefalopoulou, JG. Zhang, FG. Meng, C. Zhang, Z. Ling, A. Smeets, L. Ackermans, V. Visser-Vandewalle, A. Mogilner, M. Pourfar, W. Hu, A. Gunduz, K. Foote, M. Okun, C. Butson (Salt Lake City, UT, USA)

    Objective: We performed a retrospective analysis of Tourette syndrome (TS) patients receiving deep brain stimulation (DBS) therapy as part of the Tourette Association of America…
  • 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

    Quality of Life in Tic Disorders: An Observational, Mainstream School-Based Population Study over Time

    E. Casas-Peña, B. Ouyang, Y. Liu, E. Cubo, K. Kompoliti (Burgos, Spain)

    Objective: Our aim was to assess Quality of Life (QoL) in a sample of children assessed at two different time points, investigate the change of…
  • 2018 International Congress

    Tics in Wilson’s Disease and Review of the Literature

    AY. Yılmaz, M. Kuzu Kumcu, MC. Akbostancı (Ankara, Turkey)

    Objective: We report a case with tics in a patient with Wilson’s Disease (WD). Background: Wilson’s disease is a genetic disorder of copper metabolism, leading…
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