MDS Abstracts

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

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2018 International Congress

October 5-9, 2018. Hong Kong. Abstracts are presented on the 6th, 7th, and 8th.

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  • Non-motor symptoms in patients from the Catalonian Multiple System Atrophy Registry (CMSAR)

    D.M. Giraldo, A. Pérez Soriano, J. Rios Guillermo, E. Muñoz, Y. Compta, J. Pagonabarraga, F. Valldeoriola, J. Hernández-Vara, S. Jauma Classen, V. Puente, C. Pont, N. Caballol, E. Tolosa, A. Bayes, J. Campdelacreu, O. Fabregues, A. Avila, M. Calopa, C. Gaig, N. Fabregat, P. Pastor, M. Aguilar, M. Pujol, L. Planellas, A. Camara, M.J. Marti (Barcelona, Spain)

  • Non-motor symptoms in patients with idiopathic and converted REM Sleep Behavior Disorder

    P. Chan, W. Mao, XN. Liu, SQ. Zhan, H. Zhang, Y. Li (Beijing, China)

  • Non-motor symptoms in Spinocerebellar ataxia, multiple system atrophy and Idiopathic late-onset cerebellar ataxia

    YM. Park, MJ. Kim, SB. Koh (Seoul, Republic of Korea)

  • Non-motor symptoms of Parkinson’s disease: Evaluation of urinary disorders

    K. Karbozova. (Bishkek, Kyrgyzstan)

  • Nonlinearities in outcome-specific hazard of motor and nonmotor long-term complications of Parkinson’s disease

    P. Prange, T. Danaila, C. Laurencin, C. Caire, E. Metereau, H. Merle, E. Broussolle, D. Maucort-Boulch, S. Thobois (Bron, France)

  • Not just runners: Adult onset lower limb dystonia

    B. Karp, D. Ehrlich, K. Alter (Bethesda, MD, USA)

  • Novel biomarkers of autonomic regulation and sleep in Parkinson’s Disease derived from Network Physiology

    O. Vaou, P. Ivanof, A. DePold-Hohler, F. Lombardi, R. Endalatpour, A. Quaicoe (Boston, MA, USA)

  • Novel CACNA1A gene mutation in a Taiwan family with episodic ataxia type 2

    KF. Chen, CH. Tsai, DC. Wu (Taichung, Taiwan)

  • Novel COMT inhibitor opicapone shows sustained inhibition and improved L-DOPA availability in monkeys

    T. Kitajima, M. Bonifácio, P. Moser, P. Soares-da-Silva, M. Tanaka (Osaka, Japan)

  • Novel GBA risk factor gene mutation p.W378R in a kindred with Gaucher’s disease and Parkinson’s disease

    M. Lubomski, M. Hayes, M. Kennerson, M. Ellis, S. Chu, J. Blackie, J. O’Sullivan, G. Nicholson (Sydney, Australia)

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