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…
  • 2023 International Congress

    Human cerebellum contributes to the motor frequency coding for essential tremor and volitional rhythmic movements

    YM. Wang, A. Kumar, SH. Kuo, MK. Pan (Yun-Lin county, Taiwan)

    Objective: Tremor and volitional rhythmic movement are frequency-specific motions. However, it remains unclear which area of the central nervous system can process frequency information. This…
  • 2023 International Congress

    Gene rearrangement as the cause of hereditary Hypomyelinating Leukodyistrophy disease type 5 (HLD5)

    A. Menéndez-Albarracín, P. Pastor-Muñoz, K. Beyer, M. Gea-Rispal, D. Vilas-Roldán, R. Alvarez-Ramo, L. Ispierto-González (Barcelona, Spain)

    Objective: To define the clinical, neurophysiological, neuroimaging and pathological findings from a patient carrying a FAM126A homozygous exon 3-7 deletion. Background: Hypomyelinating leukodystrophies constitute a…
  • 2023 International Congress

    Role of the direct subthalamo-cerebellar tract in memory and learning: Implications for the pathophysiology of late-stage Parkinson’s Disease

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

    Objective: To study the role of the recently identified direct subcortical cerebellum basal ganglia (C-BG) network in the pathophysiology of Parkinson’s Disease (PD). Background: Even…
  • 2023 International Congress

    Hemidystonia of cerebellar origin

    L. Costa, J. Pinto, C. Machado, I. Amorim (Viana do Castelo, Portugal)

    Objective: To report the case of a patient developing hemidystonia in the course of cerebellar hemorrhage. Background: About 1-4% of strokes may include movement disorders,…
  • 2023 International Congress

    Rare genetic and clinical presentation of SPG7-related Hereditary Spastic Paraplegia.

    J. Hickman, E. Forbes, J. Feuerstein (DENVER, USA)

    Objective: Describe a rare genetic and clinical presentation of SPG7-related Hereditary Spastic Paraplegia. Background: SPG7-related spastic paraplegia (SPG7) is a hereditary spastic paraplegia caused by…
  • 2023 International Congress

    Unique consecutive order of brain atrophy in spinocerebellar ataxia type 3 (SCA3)

    J. Faber, T. Klockgether, H. Baumeister, D. Berron (Bonn, Germany)

    Objective: The aim was to identify the sequence of brain regions becoming atrophic in the early phase of spinocerebellar ataxia type 3 (SCA3). Background: SCA3…
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