MDS Abstracts

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

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  • 2019 International Congress

    Using Quantitative Susceptibility Mapping to Predict Dementia in Parkinson’s Disease

    G. Thomas, L. Leyland, J. Acosta-Cabronero, R. Weil (London, United Kingdom)

    Objective: To investigate how brain iron deposition relates to visual function and dementia risk in Parkinson’s Disease (PD). Background: Oxidative stress due to brain iron…
  • 2019 International Congress

    Amylin single-nucleotide polymorphism and Parkinson’s disease

    R. Valenti-Azcarate, I. Martinez-Valbuena, I. Marcilla Garcia, G. Marti, M. Carmona-Abellan, MT. Tuñon-Alvarez, MT. Luquin-Piudo (Pamplona, Spain)

    Objective: The objective of this study was to evaluate if a single nucleotide polymorphism (SNP) in the amylin sequence is present in patients with Parkinson’s…
  • 2019 International Congress

    Measuring progression of nigrostriatal degeneration in Parkinson’s disease using 18F-AV-133 vesicular monoamine transporter type-2 (VMAT2) PET

    S. Xu, V. Dore, P. Alexander, Y. Lie, S. Bozinovski, R. Mulligan, K. Young, V. Villemagne, C. Rowe (Melbourne, Australia)

    Objective: To evaluate the progression of nigrostriatal degeneration in participants with Parkinson’s disease (PD) using 18F-AV-133 vesicular monoamine transporter type-2 (VMAT2) PET. Background: Vesicular monoamine…
  • 2019 International Congress

    Clinical features of constipation in patients with Parkinson’s disease: a cross-sectional study in China

    LP. Zhu, XT. Zhou, Z. Zhou, LJ. Fang, XX. Zhou, YW. Zhao, LX. Qin, Y. Tian, ZQ. Wang, QY. Sun, Q. Xu, JC. Li, JF. Guo, XX. Yan, BS. Tang (Changsha, China)

    Objective: This study was designed to explore the clinical features of constipation, and investigate the risk factors of constipation in Chinese PD patients. Background: Constipation…
  • 2019 International Congress

    Puzzle resolution as cognitive test in Parkinson´s disease patients

    C. Borrue-Fernandez, D. Santos-García, J. Pagonabarraga, B. Pascual-Sedano, M. Mata, C. Study Group (Madrid, Spain)

    Objective: To analyze the value of puzzle resolution for cognitive testing in Parkinson´s disease patients. Background: Cognitive decline and dementia are common among Parkinson disease…
  • 2019 International Congress

    “Best practice” guidelines for the collection and analysis of speech data in patients with Parkinson’s Disease (PD).

    E. Tripoliti, L. Ramig (Boulder Colorado, CO, USA)

    Objective: To discuss the literature for collection and analysis of speech data for patients with PD in order to create “best practice” guidelines. Background: Speech…
  • 2019 International Congress

    Neuroprotective actions of red propolis extract and formononetin in a rat model of Parkinson’s disease

    M. Gomes, S. Barroso, J. de Oliveira, D. Marques, A. Santos, J. Cardoso (Aracaju, Brazil)

    Objective: To evaluate the effects of the hydroalcoholic extract of red propolis (HERP) and one of its major compounds, formononetin (FN), against the motor symptoms…
  • 2019 International Congress

    Serotonergic function in De Novo Parkinson’s Disease

    HK. Park, JJ. Lee, YM. Park (Goyang, Republic of Korea)

    Objective: We aimed to investigate the central serotonergic function in de novo PD and change in serotonergic function with dopaminergic medications. Background: While dopaminergic dysfunction…
  • 2019 International Congress

    Oscillaotory activity in the globus pallidus internus in patients with Parkinson’s disease

    P. Zhuang, M. Hallett, D. Meng, Y. Zhang, J. Li, J. Li (Beijing, China)

    Objective: To quantify the characteristics of oscillatory neurons in the GPi in patients with PD. Background: Abnormal oscillatory activity has been predicted to play a…
  • 2019 International Congress

    Phenotypic segregation in kindred with a novel ANO3 variant

    V. Carvalho, F. Correia, J. Martins, J. Massano, T. Temudo (Matosinhos, Portugal)

    Objective: To describe the phenotypic and genotypic presentation of a kindred with a novel ANO3 mutation. Background: Mutations in ANO3 gene cause an autosomal dominant…
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