MDS Abstracts

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

MENU 
  • Home
  • Meetings Archive
    • All Meetings
    • 2026 International Congress
  • Keyword Index
  • Resources
  • Advanced Search

2026 International Congress

October 4-8, 2026. Seoul, Korea.

View by Title View Categories
Jump to:  [View All] • a b c d e f g h i j k l m n o p q r s t u v w x y z
  • Genetic determinants of cognitive performance in Parkinson’s disease: impact of distal regulatory variation at the SNCA locus in the gp2 cohort

    D. Náfate Wences, A. Cervantes Arriaga, M. Rodríguez Violante, MT. Periñán Tocino, GP2. Genetics Program (Mexico City, Mexico)

  • Genetic Disorders Presenting With Tremor at Onset: MDSGene systematic literature review

    V. Alakbarzade, E. Valente, F. Morgante (Carshalton, United Kingdom)

  • Genetic Landscape of Hereditary Ataxia in a Highly Consanguineous Population: A Nationwide Multicenter Study

    F. Alqahtani, H. Alqahtani, A. Binbakheet, Z. Alqahtani, A. Sayed, A. Alsayegh, O. Alghamdi, A. Alqahtani, T. Almejaish, A. Almatrafi, A. Alhashim, A. Alotaibi, A. Kentab, R. Alshawaf, M. Abukhalid, A. Aldokheel, S. Alshimemeri, S. Alqahtani, N. Kaya, M. Rifai (Riyadh, Saudi Arabia)

  • Genetic Modifiers of Age at Onset for Parkinson’s Disease in European Populations

    H. Leonard, L. Lange, M. Makarious, A. Singleton, C. Blauwendraat (Wasington, USA)

  • Genetic modifiers of the clinical phenotype in Spinocerebellar Ataxia type 2. 25 years of candidate genes studies and the forthcoming GWAS era

    L. Almaguer-Mederos (London, United Kingdom)

  • Genetic Predictors in Dystonia: A Phenotypic Analysis.

    N. Gowda, N. Kamble, V. Holla, R. Yadav, P. Pal (Bengaluru, India)

  • Genetic Rare Variation in Early-Onset Neurodegenerative Movement Disorders: A Clinicopathologic Study.

    T. Du Toit, L. Wu, O. Serrano, N. Kuznetsov, S. Love, A. King, F. Roncaroli, L. Parkkinen, C. Morris, C. Smith, G. Serrano, T. Beach, S. Gentleman, T. Warner, Z. Jaunmuktane, J. Carr, R. Real, H. Morris (London, United Kingdom)

  • Genetic risk factors reduce the risk of diabetes mellitus in Parkinsons disease

    EK. Tan, S. Chan, B. Tan, L. Tan, C. Chan (Singapore, Singapore)

  • Genetic spectrum of spinocerebellar ataxia type 27b (atx-fgf14-gaa): a single-center study

    A. Protsenko, N. Abramycheva, E. Nuzhnyi, S. Klyushnikov, S. Illarioshkin (Moscow, Russian Federation)

  • Genetic Variation in KCNJ6 Gene Increases Risk of Impulse Disorders in Parkinson’s Disease: A Two-Cohort Study

    S. García-Díaz, J. Martín-Rodríguez, L. Muñoz-Delgado, R. Díaz-Belloso, S. Jesús, MT. Periñán, M. Martín-Bórnez, AM. Castellano-Guerrero, E. Ojeda-Lepe, D. Macías-García, A. Adarmes-Gómez, D. Buiza-Rueda, M. Bonilla-Toribio, E. Iglesias-Camacho, M. San-Eufrasio, C. Pérez-Calvo, A. Luque-Ambrosiani, F. Carrillo-García, P. Gómez-Garre, P. Mir (Sevilla, Spain)

  • « Previous Page
  • 1
  • …
  • 90
  • 91
  • 92
  • 93
  • 94
  • …
  • 208
  • Next Page »
Jump to:  [View All] • a b c d e f g h i j k l m n o p q r s t u v w x y z

Related Sites

International Parkinson and Movement Disorder Society

The Society that manages the annual International Congress »

International Congress

The official website for the International Congress of Parkinson’s and Movement Disorders® »

  • Help & Support
  • About Us
  • Cookies & Privacy
  • Wiley Job Network
  • Terms & Conditions
  • Advertisers & Agents
Copyright © 2026 International Parkinson and Movement Disorder Society. All Rights Reserved.
Wiley