MDS Abstracts

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

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Articles tagged "Basal ganglia"

  • 2023 International Congress

    Huntingtonism and bilateral basal ganglia hypointensity in a male with an XK variant but no McLeod red cell phenotype

    J. Yu, R. Walker, A. Danek, C. Westhoff, S. Vege, I. Itin (Cleveland, USA)

    Objective: To report a novel variant of XK without the characteristic RBC phenotype Background: XK disease (previously called McLeod Syndrome) is a rare X-linked disorder…
  • 2023 International Congress

    Spectrum of hyperkinetic movement disorders in a Tunisian Cohort: an observational study

    S. Laroussi, S. Daoud, N. Bouattour, S. Sakka, K. Moalla, M. Damak, N. Farhat, C. Mhiri (Sfax, Tunisia)

    Objective: Recall clinical situations of hyperkinetic movement disorders (HMD) in a Tunisian cohort. Background: HMD result from a dysfunction of the basal ganglia(BG) and are…
  • 2022 International Congress

    The role of cortical and subcortical structures in maintaining efficient network topology in Parkinson’s disease

    R. Berlot, B. Koritnik, Z. Pirtošek (Ljubljana, Slovenia)

    Objective: To assess the relative importance of cortical and subcortical nodes and their connections in maintaining efficient structural connectome topology in Parkinson's disease (PD). Background:…
  • 2022 International Congress

    A 69-year-old man with seizure-like activity and unresponsiveness

    J. Patino, A. Durand, R. Samudralwar (Houston, USA)

    Objective: Highlight the clinical features and radiologic findings of diabetic striatopathy. Background: Diabetic striatopathy is a rare condition associated with chorea and/or ballism but can…
  • 2022 International Congress

    Compound heterozygous mutation of the Beta galactosidase 1 gene presenting with familial dystonia and spondylo-epiphyseal dysplasia

    A. Elavarasi, A. Anand, A. Garg, K. Garg, M. Singh, M. Tripathi, D. Vibha, R. Singh (New Delhi, India)

    Objective: To describe a family with dystonia and spondylo-epiphyseal dysplasia Background: Childhood onset Generalized dystonia is usually associated with genetic causes. Method: We present a…
  • 2022 International Congress

    Study of age related neurodegeneration of Cerebellum Basal Ganglia direct subcortical white matter tracts using fixel-based analysis.

    V. Radhakrishnan, C. Gallea, C. Kesavadas, B. Thomas, S. Krishnan, A. Kishore (Trivandrum, India)

    Objective: The goal of the study is to use diffusion weighted imaging to confirm and expand on findings of structural tracks linking cerebellum (CB) and…
  • 2022 International Congress

    Perceive: A data extraction and analysis toolbox for brain signals from sensing enabled deep brain stimulators

    WJ. Neumann (Berlin, Germany)

    Objective: Develop an open source toolbox that facilitates data extraction, analysis, artifact correction and standardization for the DBS research community. Background: Novel sensing enabled implantable…
  • 2022 International Congress

    High frequency neck vibration changes the pallidal activity in cervical dystonia

    A. Sedov, A. Gamaleya, U. Semenova, S. Usova, R. Medvednik, A. Tomskiy, H. Jinnah, A. Shaikh (Moscow, Russian Federation)

    Objective: The aim of the current study is to characterize changes in spontaneous pallidal neuronal activity during modulation of peripheral proprioceptive input by means of…
  • 2022 International Congress

    Hyperkinesia associated with tuberculous meningitis in children: report of 2 cases.

    I. Estrada-Bellmann, E. Villarreal-Garza, C. Torres-González, B. Chávez-Luévanos, A. Cantú-Salinas, S. Castillo-Torres (Monterrey, Mexico)

    Objective: We present two pediatric patients with normal neurodevelopment, and incomplete vaccination schedule due to lack of BCG vaccine, who developed hyperkinesias secondary to tuberculous…
  • 2022 International Congress

    DBS Experience In A Pediatric Neurowilson Case

    S. Bozkaya Yilmaz, N. Olgaç Dündar, G. Basarir, P. Gencpinar, A. Ersen (Izmir, Turkey)

    Objective: I have chosen this case to demonstrate an atypical presentation of Neuro-Wilson disease without a prominent hepatic involvement. I have also aimed to call…
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