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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  • A longitudinal study of brain quantitative MRI analysis before and after diagnosis of progressive supranuclear palsy

    K. Seo, T. Yamamoto, H. Kawasaki, A. Miyake, T. Hukuoka, Y. Nakazato, T. Takahasi, I. Matunari, H. Matuda, N. Tamura, N. Araki (Saitama, Japan)

  • A machine learning approach to determine the important patient characteristics for tremor prevalence and tremor irregularity in dystonia

    S. Balta Beylergil, L. Scorr, A. Cotton, H. Jinnah, A. Shaikh (Cleveland, OH, USA)

  • A Mcleod syndrome family and novel XK gene mutation in China mainland

    L. Xu, P. Hua, W. Liu (Nanjing, China)

  • A metabolomic signature of treated and drug-naïve patients with Parkinson disease: A pilot study

    J. Troisi, A. Landolfi, C. Vitale, K. Longo, A. Cozzolino, M. Squillante, M.C. Savanelli, P. Barone, M. AmbonI (Salerno, Italy)

  • A multimodal motor skill balance training with rhythmical cues to improve and maintain balance control in Parkinson’s disease

    T. Capato, J. Nonnekes, J. Tornai, I. Kayo, J. IntHout, E. Barbosa, N. de Vries, M. Piemonte, B. Bloem (Sāo Paulo, Brazil)

  • A nationwide epidemiological study of Parkinson’s disease in Korea using national health insurance database

    WW. Lee, B. Jeon, BK. Kim, HJ. Kim (Seoul, Republic of Korea)

  • A new clinical and research smartphone application to assess tremor and bradykinesia in patients with movement disorders

    C. Duval, J.F. Daneault, B. Carignan, C.É. Coderre, S. Bogard (Montreal, QC, Canada)

  • A new distinct spastic ataxia with hypomyelination: Clinical, neuroimaging and molecular expression of NKX6-2 mutations

    V. Chelban, N. Kaya, M. Alsagob, S. Efthymiou, J. Vandrovcova, D. Lynch, K. Kloth, A. Chirita-Emandi, F. Alkuraya, N. Wood, H. Houlden (London, United Kingdom)

  • A New Scale to Measure Impairment in Patients with Writer’s Cramp

    E. Shamim, O. Ahmad, T. Wu, P. Srivanitchapoom, P. Diomi, B. Karp, K. Alter, C. Toro, B. Hodsdon, S. Pandey, J. Park, S. Meunier, M. Hallett (Largo, MD, USA)

  • A new SPG4/SPAST mutation in an Italian family with hereditary spastic paraplegia and Alzheimer’s disease

    A. Orlacchio, C. Montecchiani, R. Rumore, F. Gaudiello, M. Miele, C. Caltagirone, T. Kawarai (Rome, Italy)

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