MDS Abstracts

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

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Articles tagged "Cerebellum"

  • 2023 International Congress

    Effects of cerebellar theta burst stimulation on working memory in Parkinson’s disease

    N. Raies, J-F. Nankoo, T. Grippe, R. Chen (Toronto, Canada)

    Objective: This study aims to investigate the effects of cerebellar theta burst stimulation (TBS) on working memory (WM) performance in patients with Parkinson’s disease (PD)…
  • 2023 International Congress

    Cerebellar volumetry in SCA1, SCA3, SCA6, MSA-C, and SAOA

    M. Ferreira, T. Schaprian, T. Klockgether, J. Faber (Bonn, Germany)

    Objective: We aim to identify volume differences in the cerebellum between spinocerebellar ataxia type 1 (SCA1), SCA3, SCA6, multiple-system atrophy, cerebellar type (MSA-C), and sporadic…
  • 2023 International Congress

    Automated parcellation of the cerebellum in patients with newly diagnosed Parkinson’s disease

    B. Facer, C. de Bezenac, A. Macerollo, T. Butts, R. Sadavarte, J. Farah, S. Keller (Liverpool, United Kingdom)

    Objective: Quantitatively evaluate the gross morphology of individual cerebellar lobules, determine whether cerebellar anatomical changes occur early in the disease and whether changes were related…
  • 2023 International Congress

    cerebellar cognitive affective syndrome is frequent in rfc1-related disorder

    C. Lobo, NB. Santos, F. Lima, T. Rezende, PC. Matos, JL. Pedroso, O. Barsottini, W. Marques Jr, M. França Jr (Campinas, Brazil)

    Objective: To describe the prevalence and clinical profile of cerebellar cognitive affective syndrome (CCAS) in patients with RFC1-related disorder. Background: Since the recent description of…
  • 2022 International Congress

    Clinical and genetic characterization of two Portuguese families with spinocerebellar ataxia 48

    MJ. Lima, AR. Silva, P. Bem, C. Cruto, S. França, M. Rodrigues, A. Rua, M. Reis, J. Freixo, J. Oliveira, P. Salgado, M. Calejo (Senhora da Hora, Portugal)

    Objective: Genetic and phenotypic characterization of six patients from two families, with pathogenic variants on the STUB1 gene. Background: Biallelic pathogenic variants on the STUB1…
  • 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

    Detection of specific antigens in immune-mediated cerebellar ataxias

    A. Kudo, H. Yaguchi, M. Abe, A. Nagai, S. Shirai, I. Takahashi-Iwata, M. Matsushima, M. Watanabe, S. Hatakeyama, I. Yabe (Sapporo, Japan)

    Objective: We aimed to clarify biomarkers and pathogenic autoantibodies in cerebellar ataxia, especially multiple system atrophy (MSA) and immune-mediated cerebellar ataxias (IMCAs), by detection of…
  • 2022 International Congress

    Challenging diagnosis of familial Gerstmann-Straussler-Scheinker disease with normal brain image: a case report and systematic review

    KY. Park, SY. Jo, SJ. Chung (Seoul, Republic of Korea)

    Objective: We report a case of familial Gerstmann-Straussler-Scheinker (GSS) disease, who presented with cerebellar ataxia, but did not show abnormalities in diffusion weighted image (DWI)…
  • 2022 International Congress

    Impaired reinforcement learning in patients with cerebellar ataxia

    J. Nicholas, CJ. Amlang, CY. Lin, N. Desai, L. Montaser-Kouhsari, SH. Kuo, D. Shohamy (New York, USA)

    Objective: To further characterize cerebellar learning processes as well as learning impairment pattern in patients with cerebellar dysfunction. Background: Supervised learning (i.e., learning from error)…
  • 2022 International Congress

    Clinical and Genetic spectrum of a series of congenital ataxias patients.

    R. Baviera-Muñoz, L. Carretero-Vilarroig, M. Campins-Romeu, C. Morata, I. Sastre-Bataller, N. Muelas, I. Martínez-Torres, M. Tomás-Vila, T. Jaijo, E. Aller, L. Bataller (Valencia, Spain)

    Objective: To describe the clinical and molecular findings of a well-defined group of 11 congenital ataxia patients from 12 different families assessed in an adult…
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