MDS Abstracts

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

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  • 2024 International Congress

    Cortical response to proprioceptive stimulation in orthostatic tremor – a magnetoencephalography study

    K. Af Edholm, M. Vinding, C. Pfeiffer, D. Lundqvist, J. Waldthaler (Danderyd, Sweden)

    Objective: To investigate cortical integration of proprioceptive information in patients with orthostatic tremor (OT), measured as event-related synchronisation (ERS) response to proprioceptive stimulation using magnetencephalography…
  • 2024 International Congress

    Secondary orthostatic tremor associated with hyperthyroidism: A case report

    T. Dang, K. Vo, T. Tran (HO CHI MINH, Viet Nam)

    Objective: To illustrate the electrophysiological and clinical findings in a patient with secondary orthostatic tremor (OT) associated with hyperthyroidism Background: Orthostatic tremor is a rare…
  • 2024 International Congress

    Movement Disorders Associated with Infectious Encephalitis in Pediatric Patients

    M. Mnif, H. Benrhouma, T. Benyounes, H. Klaa, Z. Miladi, A. Zioudi, I. Turki, I. Kraoua (Tunis, Tunisia)

    Objective: The objective of our study is to report the clinical and imaging profile of a cohort of pediatric patients with movement disorders (MDs) associated…
  • 2024 International Congress

    Expanding the phenotypic spectrum of movement disorders in 22q11.2 deletion syndrome

    N. Reyes, T. Cortez-Grippe, M. Callister, T. Heung, A. Bassett, A. Lang (Toronto, Canada)

    Objective: To formally characterize the evolving spectrum of movement disorders associated with chromosome 22q11.2 deletion syndrome Background: Emerging evidence suggests that a wide range of…
  • 2024 International Congress

    The functional consequences of the ‘African GBA1 allele’ of rs3115534 in Parkinson’s Disease

    M. Radefeldt, L. Demuth, R. Al-Ali, S. Fischer, C. Beetz, P. Bauer (Rostock, Germany)

    Objective: To gain insights into the pathophysiology by which the G-allele of rs3115534 confers risk for PD. Background: A recent paper defined the G-allele of…
  • 2024 International Congress

    RAB32 c.213C>G (p.Ser71Arg) explains Parkinson’s disease in two UK families: description of the clinical and biochemical features

    R. Tilney, R. Real, E. Gustavsson, S. Jasaityte, Y. Kordovska, M. Fenn, P. Korlipara, M. Hu, E. Sammler, M. Farrer, H. Morris (London, United Kingdom)

    Objective: To describe the clinical features, family structure of two families identified to have the recently described pathogenic variant RAB32 c.213C>G (p.Ser71Arg). Background: Genetic mutations…
  • 2024 International Congress

    Utilizing a global network to study environmental factors relating to Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

    K. Atterling Brolin, L. Jones, B. Fiske, S. Jasaityte, H. Morris, A. Noyce (Lund, Sweden)

    Objective: To identify and collect data on non-genetic variables from individuals with and without Parkinson’s disease (PD) in the Global Parkinson’s Genetics Program (GP2, http://gp2.org/).…
  • 2024 International Congress

    Parkinson’s Disease Risk Genotypes at the GPNMB Locus Associate with Extent of Post-mortem Lewy Pathology

    E. Brody, E. Suh, V. van Deerlin, J. Trojanowski, E. Lee, A. Chen-Plotkin (PHILADELPHIA, USA)

    Objective: To determine whether Parkinson’s disease (PD) risk genotypes at the GPNMB locus associate with distribution of Lewy pathology in brain samples from a spectrum…
  • 2024 International Congress

    5HTTLPR (44bp Ins/Del) polymorphism: Serotonergic subtype of Parkinson’s Disease

    T. Syed, R. Kandadai, S. Yaranagula, T. Sd, S. Mohareer, S. Kola, R. Alugolu, R. Borgohain (Hyderabad, India)

    Objective: To find out the association of 5HTTLPR (44bp Ins/Del) polymorphism with PD neurotransmitter subtypes Background: Parkinson’s Disease (PD) can be sub divided into serotonergic,…
  • 2024 International Congress

    A Case of Paradoxical Gait Response to Levodopa in Parkin-Gene-Related Early-Onset Parkinson’s Disease

    D. Naheed, A. Mehta, S. Neo, L. Tan (Singapore, Singapore)

    Objective: We present a case with a paradoxical gait response to levodopa in Parkin gene-related early-onset Parkinson's Disease. Background: Parkin (PRKN) mutations are the predominant…
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