MDS Abstracts

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

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  • 2024 International Congress

    Use of social media and health information technology among caregivers of Alzheimer’s disease and other neurological conditions: Secondary analysis of the 2022 Health Information National Trend (HINTS) Survey

    M. Arbabi Kalati (Hinsdale, USA)

    Objective: This study aims to evaluate the pattern of health information seeking from social media and other health technology tools among caregivers for individuals with…
  • 2024 International Congress

    Speech Processing System for Parkinson’s Disease Using Mixed Reality

    M. Wójcik-Pędziwiatr, M. Dudek, W. Skibicka, M. Rudzińska-Bar, M. Danioł, P. Jemioło, J. Stępień, D. Hemmerling (Cracow, Poland)

    Objective: Our initiative aims to develop an integrated AR/MR platform for collecting diagnostic data and monitoring patients with neurodegenerative diseases using digital markers from registered…
  • 2024 International Congress

    Nonmotor symptoms in Spinocerebellar ataxia type 12 (SCA 12)

    S. Choudhury, P. Basu, S. Mondal, R. Banerjee, J. Ganguly, M. Tiwari, H. Kumar (Kolkata, India)

    Objective: To find the frequency and extent of depression, autonomic disturbances, and cognitive impairment in patients with SCA12 and exploring its association with motor symptoms…
  • 2024 International Congress

    Evaluating Pharmacological Interventions for Friedreich Ataxia: A Network Meta-Analysis of Randomised Trials

    T. Dave, V. Kumar, R. Raj, MA. Shamim, V. Suresh, K. Patel, M. Hassan, A. Bhonsale, DVV. Krishna, B. Dhakal, A. Ambulinambi, D. Dey (Chernivtsi, Ukraine)

    Objective: To compare the clinical efficacy of different pharmacological agents in reduction of disease severity of Friedreich Ataxia. Background: Friedreich ataxia is a rare, inherited,…
  • 2024 International Congress

    NGS diagnosis rate in a combined cerebellar ataxia and spastic paraplegia series from southern Spain

    A. Adarmes Gómez, S. Jesús Maestre, D. Macias Garcia, F. Carrillo Garcia, L. Muñoz Delgado, P. Gómez Garre, P. Mir (Sevilla, Spain)

    Objective: To evaluate the diagnosis rate of Next Generation Sequencing (NGS) in a combined series of patients with progressive cerebellar ataxia (CA) and progressive spastic…
  • 2024 International Congress

    Pulmonary Dysfunction in Friedreich’s Ataxia (FRDA)

    T. Zesiewicz, T. Vu, A. Patel, T. Mcdonald, Y. Huang, Y. Zhao, L. Campbell, L. Evans, D. Mohan, C. Gooch, K. Calero (Tampa, USA)

    Objective: We sought to characterize pulmonary function in FRDA and identify disease variables that may contribute to dysfunction. Background: FRDA is a neurodegenerative disease that causes…
  • 2024 International Congress

    Empower-PD: “An Exploratory Investigation of Accelerometer Data on Parkinson’s Patients’ Motor Symptoms and the Correlation with Quality of Life.”

    M. Hansen, B. Sørensen, T. Thomsen, N. Karottki (Copenhagen, Denmark)

    Objective: To describe weekly changes in bradykinesia-score (BKS) measured on objective wearable data and assess the correlation between these changes and Quality of Life (QoL)…
  • 2024 International Congress

    Two-year longitudinal evaluation of ataxia and brain structural changes in RFC1-related disorder

    C. Lobo, T. Rezende, G. Schmitt, P. Matos, F. Lima, A. Martinez, O. Barsottini, JL. Pedroso, W. Marques Jr, M. França Jr (Campinas, Brazil)

    Objective: To describe the evolutionary pattern of brain structural changes in patients with RFC1-related disorder. Background: Specific brain structural changes have been described in patients…
  • 2024 International Congress

    Oculomotor Biomarkers for Cerebellar Ataxia and Severity in Smooth Pursuit

    P. Ponger, G. Gurevich, R. Alcalay, Y. Bonneh, S. Shani (Tel Aviv, Israel)

    Objective: Our research utilizes the technique of brief linear smooth pursuit of a moving target, to derive various parameters. These parameters are then analyzed to…
  • 2024 International Congress

    Spinocerebellar Ataxia Type 4: a Novel Polyglycine Disease caused by GGC Repeat Expansion in ZFHX3.

    S. Pulst (slc, USA)

    Objective: Identification of the mutation causing SCA4. Background: SCA4 is an autosomal dominant disease, originally described in a large Utah pedigree, characterized by sensory and…
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