MDS Abstracts

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

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  • 2024 International Congress

    Association of cognition and other clinical characteristics of individuals with Essential Tremors

    H. Khalil, M. Nazzal, A. Al-Sharman, D. Al-Shorafat, H. Al Refa’I, S. Obeidat, L. Samman, K. El-Salem (Doha, Qatar)

    Objective: To examine the correlation between cognition and other clinical characteristics (motor and non-motor) in people with Essential Tremor. To examine the correlation between cognition and…
  • 2024 International Congress

    Feasibility of Reliable, Remote Assessment of a 13-year-old Boy Who Stopped Talking

    N. Kadubandi, A. Elshourbagy, J. Brašić (Baltimore, USA)

    Objective: To assess the feasibility of reliable, remote assessments of videos of a 13-year-old boy who stopped talking Background: The sudden absence of speech in…
  • 2024 International Congress

    Utility of Whole Exome Sequencing in movement disorders potentially related to Mitochondrial cytopathies

    D. Dhar, V. Holla, P. Phulpagar, R. Yadav, N. Netravathi, B. Muthusamy, P. Pal (Bangalore, India)

    Objective: To describe the clinic-genetic profile of clinically suspected mitochondrial cytopathies with movement disorders (MDs). Background: Literature on the clinico-genetic spectrum of movement disorders related…
  • 2024 International Congress

    Investigating the genetic relationship between vitamin B12 deficiency and Parkinson’s disease

    K. Senkevich, R. Dering, M. Onvumere, L. Liu, P. Huot, Z. Gan-Or (Montreal, Canada)

    Objective: The aim of this study was to investigate the genetic association and causal link between vitamin B12 and the risk and progression of Parkinson's…
  • 2024 International Congress

    The First of Its Kind Genetics Cohort: the Black and African American Connections to Parkinson’s Disease (BLAAC PD) Study

    N. Louie, J. Solle, S. Bandrés-Ciga (New York, USA)

    Objective: Recruit and characterize a Black and African American (BAA) cohort to better understand Parkinson’s disease (PD). Background: A significant gap exists in our understanding…
  • 2024 International Congress

    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)

    Objective: Our objective is to undertake the most extensive screening of the impact of homozygosity in Parkinson's disease (PD) etiology across diverse populations. We aim…
  • 2024 International Congress

    Latent Genetic Architecture of Parkinson’s Disease Risk factors and Comorbidities

    J. Kim, I. Foote, S. Bandres-Ciga, 23. Research Team, C. Marshall, A. Grotzinger3, A. Singleton, A. Brentnall, C. Blauwendraat, A. Noyce, G. Genetics Program (London, United Kingdom)

    Objective: To comprehensively investigate the genetic relationship between Parkinson’s disease (PD), its risk factors, and comorbidities by constructing a factor model of the shared genetic…
  • 2024 International Congress

    Clinico-genetic profile of five patients with PARK-PINK1: A case series from India

    A. Gunasekaran, P K. Pal, R. Yadav, N. Kamble, V. Holla (Bangalore, India)

    Objective: The aim of our study is to describe the clinical features and genetic profile of patients of PARK-PINK1 and to draw correlation with genetic…
  • 2024 International Congress

    The association of Severity and Monogenetic Subgroups in Parkinson’s Disease

    N. Pacheco-Barrios, K. Acurio, J. Rolston, T. Siepman, B. Illigens (Boston, USA)

    Objective: Explore how different genotypes can affect the disease severity and progression in Parkinson's patients. Background: Genetic advances have identified specific mutations linked to disease…
  • 2024 International Congress

    Hemochromatosis and Movement Disorders

    P J. Garcia Ruiz, C. Garcia Campos, C. Feliz, J. Del Val, J. Montoya (Torrelodones, Spain)

    Objective: To describe a  series (clinical  and imaging)  of movement disorders occurring in  patients with hemochromatosis Background: Hemochromatosis is a frequent disease, characterized by deposits…
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