MDS Abstracts

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

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  • 2016 International Congress

    Esophageal involvement in multiple system atrophy

    T. Shimohata, H. Taniguchi, H. Nakayama, K. Hori, M. Inoue, M. Nishizawa (Niigata, Japan)

    Objective: To determine the prevalence of esophageal involvement and its impact on clinical manifestations in patients with multiple system atrophy (MSA). Background: Secondary motor disorders…
  • 2016 International Congress

    Deep brain stimulation of the dentate nucleus improves ataxia and modulates cortical excitability

    C.C. França, M.J. Teixeira, D. Ciampi de Andrade, R. Galhardoni, V.R. Barboza, V. Silva, G. Lepski, E.R. Barbosa, R.G. Cury (São Paulo, Brazil)

    Objective: To assess tremor and ataxia changes by dentate nucleus deep brain stimulation and evaluate how DBS could modulate cortical excitability seen in cerebellar stroke.…
  • 2016 International Congress

    Evaluation of parkinsonism and striatal dopamine transporter loss in patients with spinocerebellar ataxia type 6

    T. Xie, D. Appelbaum, J. Bernard, M. Padmanaban, Y. Pu, C. Gomez (Chicago, IL, USA)

    Objective: To study whether spinocerebellar ataxia type 6 (SCA6) patients have parkinsonism and striatal dopamine transporter (DAT) loss compared to gender- and age-matched healthy controls.…
  • 2016 International Congress

    Modelling spinocerebellar ataxia 15 with iPS cell derived neurons

    S. Wiethoff, C. Arber, S. Wray, Y. Zhi, R. Patani, H. Henry (London, United Kingdom)

    Objective: Here we set out to study the cellular pathology of ITPR1-deletions underlying SCA15 in a human model of iPSC-derived cortical neurons. Background: Spinocerebellar Ataxia…
  • 2016 International Congress

    Sub-acute rapidly progressive cerebellar ataxia – A case of JC virus associated granule cell neuronopathy (GCN)

    V.K. Palmadottir, J.A. Gold, N. Vora, C.W. Kilbane (Stanford, CA, USA)

    Objective: To describe a case of JC virus associated GCN. Background: JC virus associated CNS disease most commonly presents as progressive multifocal leukoencephalopathy. A less…
  • 2016 International Congress

    Impaired eye voice coordination in spinocerebellar degeneration while reading aloud

    Y. Terao, S. Tokushige, S. Terada, T. Sasaki, M. Hamada, S. Tsuji, Y. Ugawa (Tokyo, Japan)

    Objective: In order to elucidate the cause of the impaired reading performance. Background: Deficit in reading performance in patients with spinocerebellar degeneration (SCD) has been…
  • 2016 International Congress

    Natural history of saccadic abnormalities in spinocerebellar ataxia 2: Implications to designing future clinical trials

    R. Rodríguez-Labrada, L. Velázquez-Pérez, G. Auburger, U. Ziemann, Y. Vazquez-Mojena, N. Canales-Ochoa (Holguín, Germany)

    Objective: The present study was aimed to assess the progression of saccade involvement in SCA2 patients, identify its main determinants and evaluate its usefulness as…
  • 2016 International Congress

    Relationship between sensory augmentation and exercise routine in the improvement in balance and gait in a patient with lithium-induced ataxia

    M.D. Maldonado (Santiago, Chile)

    Objective: This case report describes the use of sensory augmentation and an exercise routine to improve balance and gait in a patient with lithium-induced ataxia.…
  • 2016 International Congress

    Prodromal criteria of spinocerebellar type 2: Lessons for physiopathology, natural history and therapeutical trials

    L. Velázquez-Pérez, R. Rodríguez-Labrada, N. Canales-Ochoa, J. Fernandez-Ruiz, J. Medrano-Montero, Y. Vazquez-Mojena, G. Auburger, U. Ziemann (Holguín, Cuba)

    Objective: To identify criteria defining the prodromal stage of spinocerebellar ataxia 2 (SCA2). Background: The prodromal stage of spinocerebellar ataxias has not been systematically studied…
  • 2016 International Congress

    The aetiology of idiopathic late onset cerebellar ataxia

    R. Barbosa, M. Mendonça, T. Lampreia, P. Bugalho (Lisboa, Portugal)

    Objective: Assess the prevalence and compare clinical features of SAOA, MSA and sporadic ataxia patients with a genetic diagnosis in ILOCA patients. Background: Cerebellar ataxias…
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