MDS Abstracts

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

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Articles tagged "Cerebellum"

  • 2017 International Congress

    Does cerebellar dysfunction contribute to tremor in Parkinson’s disease?

    E. Batzianouli, M. Pagliaro, D. Benninger (Lausanne, Switzerland)

    Objective: This study aims to investigate the potential role of cerebellar dysfunction in the pathogenesis of tremor in Parkinson’s disease (PD). Background: Rest tremor in…
  • 2017 International Congress

    Gray Matter Density in Essential Tremor: A Lobule by Lobule Analysis of the Cerebellum

    E. Louis, J. Dyke, E. Cameron, N. Hernandez, U. Dydak (New Haven, CT, USA)

    Objective: Our hypothesis was that regional differences in cerebellar gray matter (GM) density may better distinguish essential tremor (ET) cases from controls.  Background: The pathophysiological…
  • 2017 International Congress

    Prism adaptation and cerebellar inhibition were impaired in essential tremor

    R. Hanajima, R. Tsutsumi, Y. Shirota, T. Shimizu, N. Tanaka, Y. Ugawa (Kanagawa, Japan)

    Objective: We aimed to reveal cerebellar dysfunction in patients with essential tremor using neurophysiological methods. Background: Cerebellar dysfunction is suggested to contribute to tremor generation.…
  • 2017 International Congress

    Cerebello-cortical loops differ between Essential-, Parkinsonian- and voluntary tremor

    J. Raethjen, M. Muthuraman, S. Groppa, G. Deuschl (Kiel, Germany)

    Objective: Topographical comparison of subcortico-cortical oscillating loops between different tremors.    Background: Cerebellum and cortical motor regions are involved in Essential, Parkinsonian and voluntary tremor, three oscillatory motor…
  • 2017 International Congress

    Wearable gait sensors to measure degenerative cerebellar ataxia

    R. Sakakibara, K. Terayama, O. Akihiro, H. Haruta, T. Akiba, F. Tateno, M. Kishi, Y. Tsuyusaki, Y. Aiba, T. Ogata (Sakura, Japan)

    Objective: We aimed to correlate a bed-side ataxia measure with wearable gait sensors parameters in cerebellar ataxia patients.  Background: Limited attention has been paid to…
  • 2017 International Congress

    Investigating the Lipidomic Signature of Spinocerebellar Ataxia (SCA1) Using A Liquid-Microjunction Surface Sampling Probe

    V. Vedam-Mai, E. Gill, M. Marks, R. Yost, T. Garrett (Gainesville, FL, USA)

    Objective: Lipidomic analysis of mice with spinocerebellar ataxia by mass spectrometry. Background: Ataxia is a movement disorder affecting balance and coordination of limbs, gait, eyes…
  • 2017 International Congress

    Impaired cerebellum to motor cortex associative plasticity in patients with spinocerebellar ataxia type 3

    M.-K. Lu, J.-C. Chen, C.-M. Chen, C.-H. Tsai (Taichung, Taiwan)

    Objective: This study aims to investigate the associative plasticity induced by cerebellum to primary motor cortex (CB-->M1) corticocortical paired associative stimulation (PAS) in patients with…
  • 2017 International Congress

    Effects of TRH therapy on the prism adaptation task in patients with spinocerebellar degeneration.

    T. Shimizu, R. Hanajima, R. Tsutsumi, K. Shimizu, N. Tominaga, Y. Ugawa, K. Nishiyama (Sagamihara, Japan)

    Objective: To reveal effects of TRH therapy on the prism adaptation task in patients with spinocerebellar degeneration (SCD). Background: TRH [Thyrotropin releasing hormone (protirelin tartrate)]…
  • 2017 International Congress

    Noninvasive cerebellar stimulation for adults with cervical dystonia

    A. McCambridge (Sydney, Australia)

    Objective: To examine whether a 5 day treatment period of anodal transcranial direct current stimulation (a-tDCS) over the cerebellum would improve patients’ symptoms and alter…
  • 2017 International Congress

    Motor stress elicits dystonia-like movements in a pharmacological mouse model for Rapid-Onset Dystonia-Parkinsonism (DYT12)

    L. Rauschenberger, J. Volkmann, C.W. Ip (Wuerzburg, Germany)

    Objective: To study if a mild stressful trigger by motor activity leads to development of dystonia-like movements in a pharmacological mouse model for DYT12. Background:…
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