MDS Abstracts

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

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2019 International Congress

September 22-26, 2019. Nice, France.

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  • A Large-Scale Survey of Rock Steady Boxing (RSB) Utilization in Parkinson’s Disease

    D. Bega, D. Larson, M. Rafferty (Chicago, IL, USA)

  • A Lewy body disease of widely confirmed Lewy bodies in the cerebral cortexes including the occipital lobe without pathological changes in the hippocampal CA2/3 region

    M. Ryo, K. Hasegawa, I. Saitoh, S. Yagishita (Tokyo, Japan)

  • A life-threatening case of Anti-IgLON5 disease

    M. Filidei, N. Tambasco, F. Paolini Paoletti, S. Simoni, E. Brahimi, G. Cappelletti, P. Nigro, P. Calabresi (Perugia, Italy)

  • A machine learning approach to predict non-responders to subthalamic nucleus deep brain stimulation in Parkinson disease patients based on preoperative characteristics

    J. Habets, M. Janssen, A. Duits, B. de Greef, A. Mulders, L. Sijben, Y. Temel, M. Kuijf, P. Kubben, C. Herff (Maastricht, Netherlands)

  • A Multiple Ascending-Dose Study of LY3154207, A Dopamine D1 Receptor Positive Allosteric Modulator (D1PAM)

    K. Biglan, D. Wilbraham, K. Svensson, M. Tsai, W. Kielbasa (Indianapolis, IN, USA)

  • A Neuroscientific approach for MCI Characterization using a Motor and Cognitive Dual-Task

    G. Mancioppi, F. Fiorini, M. Timpano Sportiello, E. Rovini, F. Cavallo (Pontedera, Italy)

  • A new screening tool to detect psychoaffective states in patients with Parkinson´s disease

    C. Schedlich-Teufer, M. Sommerauer, S. Jost, S. Schnitzler, H. Dafsari, E. Kalbe, J. Kessler, M. Barbe (Cologne, Germany)

  • A novel heterozygous ANO3 mutation responsible for myoclonus-dystonia

    C. Laurencin, E. Broussolle, T. Danaila, M. Anheim, J. Chelly, S. Thobois (Lyon, France)

  • A novel intermittent control paradigm to investigate oscillatory neuronal activity in the STN

    M. Boca, N. Ray, C. Kobylecki, J. Evans, I. Loram, M. Silverdale (Manchester, United Kingdom)

  • A novel intronic pentanucleotide TTTGA repeat insertion in SAMD12 causes familial cortical myoclonic tremor with epilepsy type 1

    ZD. Cen, Y. Chen, S. Chen, XH. Chen, B. Wang, F. Xie, OY. Zhiyuan, ZW. Jiang, AS. Fu, B. Hu, HM. Yin, X. Qiu, F. Yu, XP. Du, WC. Has, YX. Liu, HT. Wang, DH. Yang, LB. Wang, CY. Liu, JF. Xiao, BR. Zhang, W. Luo (Hangzhou, China)

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