MDS Abstracts

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

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2024 International Congress

September 27-October 1, 2024. Philadelphia, PA.

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  • Genetic determinants of the progression of Lewy body pathology

    L. Wu, AL. Gil, T. Georgiades, E. Stafford, K. Levine, M. Tan, A. Martinez Carrasco, D. Gveric, N. Wood, C. Smith, A. King, S. Love, A. Robinson, L. Parkinnen, C. Morris, J. Tunold, M. Nalls, C. Blauwendraat, A. Singleton, G. Halliday, C. Shepherd, S. Gentleman, T. Warner, Z. Jaunmuktane, L. Pihlstrom, J. Hardy, T. Lashley, R. Real, H. Morris (London, United Kingdom)

  • Genetic Heterogeneity in Chorea-Acanthocytosis Revealed by Varying VPS13A Mutations Within a Consanguineous Family

    S. Alatrash, F. Farook, D. Nicholl (Newcastle-Under-Lyme, United Kingdom)

  • Genetic Migration Dynamics: Unraveling the Influence of Internal Migration on Huntington’s Disease Prevalence in the Amazonas State.

    M. Della Coletta, C. Camargo, D. Brito, C. Fantin, G. Benevides, D. Cruz, M. Evangelista, F. Carvalho, M. Teles, D. Reis, E. Amaral, H. Teive (Manaus, Brazil)

  • Genetic Modifiers of Age at Onset for Parkinson’s Disease in Chinese Population

    H. Pan, L. Liu, J. Guo, B. Tang, Y. Zhao (Changsha, China)

  • Genetic signatures stratify PwP into three subgroups with differing responses in two disease-modifying Phase 3 trials and indicate multiple disease biology pathways to Parkinson’s Disease

    K. Hill, J. Cooper, J. Kozlowska, N. Olsen, R. Sultana, J. Surmeier, R. Wyse, N. Humphryes-Kirilov, A. Cooper (Sydney, Australia)

  • Genetic Study of polymorphism of cytokines in Parkinson’s disease.

    S. Frikha, O. Ben Othmen, S. Fezai, A. Achouri, M. Ben Mahmoud, S. Fray, H. Jamoussi, M. Fredj, N. Ben Ali (Tunis, Tunisia)

  • Genetic Variant in the VPS16 Gene in a 44-year-old Patient with Generalized Dystonia

    A. Sanguinetti, A. Tschopp, G. Ziegler, G. Povedano (Bueno Aires, Argentina)

  • Genetic Variants and Levodopa Response in Parkinson’s Disease: Insights from MAO-B and DAT1 Polymorphisms

    S. Sarkar, A. Biswas, S. Ansari, S. Sengupta, S. Choudhury, R. Banerjee, S. Chatterjee, S. Dey, H. Kumar (Kolkata, India)

  • Genome-wide Assessment of Homozygosity in Parkinson’s Disease Across Diverse Ancestral Population

    K. Step, C. Hernandez Astudillo, E. Eltaraifee, Z-H. Fang, A. Hernández-Medrano, P-J. Kung, M. Ostrožovičová, A. Zirra, I. Sarmiento, S. Bandres-Ciga (Cape Town, South Africa)

  • Genome-Wide Association Study revealing novel risk loci associated with Age at Onset of Parkinson’s Disease

    YS. Hwang, SY. Jo, SH. Lee, KY. Park, SJ. Chung (Jeonju, Republic of Korea)

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