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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  • Gender effects on clinical features in LRRK2 G2385R carriers and non-carriers in Parkinson’s disease

    S. Cui, S. Chen (Shanghai, People’s Republic of China)

  • Gender-specific pattern of sensori-motor network connectivity in early untreated Parkinson’s disease patients

    R. De Micco, F. Esposito, F. Di Nardo, A. De Mase, G. Caiazzo, A. Giordano, M. Siciliano, G. Tedeschi, A. Tessitore (Naples, Italy)

  • Generalized chorea in a patient with isolated leukocytosis and JAK2V617F mutation: A case report

    S. Bette, H. Moore, C. Singer (Miami, FL, USA)

  • Generalized choreoathetoid-like movements in primary Sjögren syndrome

    N. Alvarado-Franco, L. Olguín-Ramírez, A. Garza-Alpirez, G. Femat-Roldan, D. Martinez-Ramirez (Monterrey, Mexico)

  • Generalized dystonia and chorea with family history: Clinical case

    R. Varela, R. Araújo, M. Sousa, I. Alonso, A. Morgadinho, I. Fineza (Coimbra, Portugal)

  • Generation and in-depth characterization of induced pluripotent stem cell (iPSC) lines from 10 affected and unaffected carriers of THAP1 mutations

    H. Baumann, M. Trilck, M. Jahn, A. Münchau, V. Kostic, C. Klein, P. Seibler, K. Lohmann (Luebeck, Germany)

  • Genetic analysis of Wilson’s disease in Taiwan

    T.H. Yeh, C.S. Lu, C.C. Huang, S.C. Lai (Taipei, Taiwan)

  • Genetic defects causing complex movement disorders and basal ganglia degeneration in childhood

    H. Baide-Mairena, L. Martí-Sánchez, J. Muchart, M. Rebollo, E. Turón, JC. Cabrera López, Y. Tong-Hong, M. Madruga-Garrido, O. Alonso-Luengo, P. Quijada-Fraile, M.T. García-Silva, A. Cerisola, R. Velazquez-Fragua, E. Schuler, E. López-Laso, L. Gutiérrez-Solana, C. Cáceres-Marzal, I. Marti, O. García-Campos, M. Tomas-Vila, A. Macaya, H. Ben-Pazi, G.I. Rice, Y. Crow, R. Pons, J.D. Ortigoza-Escobar, B. Pérez Dueñas (Barcelona, Spain)

  • Genetic Markers of Essential Tremor in Restless Legs Syndrome/Willis-Ekbom Disease in Southern Chinese Population

    G. Li, HD. Tang, P. Huang, YC. He, C. Wang, XM. Qi, J. Chen, JF. Ma, SD. Chen (Shanghai, China)

  • Genetic variations of SNCA and striatal dopaminergic dysfunction in patients with Parkinson’s disease

    MJ. Lee, K. Pak (Busan, Korea)

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