MDS Abstracts

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

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MDS Virtual Congress 2020

September 12-16, 2020. Virtual Congress. www.mdscongress.org

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  • Gender-related differences in nonmotor symptoms in the context of subthalamic stimulation in Parkinson’s disease

    L. Strobel, S. Jost, A. Sauerbier, A. Rizos, K. Ashkan, M. Silverdale, J. Evans, P. Loehrer, F. Rosenkranz, M. Barbe, G. Fink, M. Samuel, K. Ray Chaudhuri, A. Antonini, P. Martinez-Martin, L. Timmermann, V. Visser-Vandewalle, H. Dafsari (Cologne, Germany)

  • Genetic analysis of Huntington’s Disease in a Brazilian Amazonian population

    D. Brito, M. Della Coletta, G. Ferreira, L. Amorim, S. Souza, S. Peixoto, C. Rezende (Manaus, Brazil)

  • Genetic and environmental prognostics of cognitive trajectories in patients with Parkinson’s disease

    S. Jo, K.W Park, S.H Lee, Y.S Hwang, S.J Chung (Seoul, Republic of Korea)

  • Genetic Profiling of Early Synucleinopathy in Rat Nigrostriatal Dopamine Neurons

    J. Patterson, C. Kemp, M. Duffy, J. Howe, C. Russell, A. Stoll, K. Miller, J. Beck, S. Counts, K. Steece-Collier, K. Luk, C. Sortwell (Grand Rapids, MI, USA)

  • Genetic risk scores and hallucinations in Parkinson’s disease patients

    C. Kusters, K. Paul, A. Duarte Folle, A. Keener, J. Bronstein, V. Dobricic, O.B Tysnes, L. Bertram, G. Alves, J. Sinsheimer, C. Lill, J. Maple-Grødem, B. Ritz (Los Angeles, CA, USA)

  • Genetic testing in pediatric dystonia and influence of clinical factors on diagnostic yield

    T. Larsh, H. Fernandez, M. Aldosari (Cleveland, OH, USA)

  • Genetic, biochemical and clinical findingss in Friedreich’s ataxia patients – relationship with the disease severity

    R. Moganty, D. Pathak, A. srivastava, s. Gulati (New Delhi, India)

  • Genome-wide association studies of progression in Parkinson’s disease

    M. Tan, M. Shoai, M. Lawton, S. Kanavou, N. Wood, J. Hardy, Y. Ben-Shlomo, N. Williams, M. Hu, D. Grosset, H. Morris (London, United Kingdom)

  • Gerstmann-Sträussler-Scheinker disease presenting as a late onset slowly progressive spinocerebellar ataxia: expanding the phenotypic spectrum of genetic prion disease

    C. Stephen, J. Chen, B. Appleby, T. Prior, M. Frosch, J. Schmahmann (Boston, MA, USA)

  • Glucocerebrosidase activity and atypical parkinsonism: a multi-centre exploratory study

    R. Alvarez Velasco, P. Giraldo, P. Irun, L. Vela Desojo, L. Lopez Manzanares, J.M Arbelo González, M. Eimil Ortiz, A. Rojo Sebastian, M. Mata Álvarez-Santullano, I. Martínez Torres, J. Garcia-Caldentey, M. Gómez Gutierrez, C. Estévez-Fraga, J.L López Sendón, G. García Ribas, J.C Martínez Castrillo, A. Alonso-Canovas (Madrid, Spain)

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