MDS Abstracts

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

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  • 2026 International Congress

    An International Consensus Framework for Computer Vision-ready acquisition and reporting: Toward Measurement-grade video in Neurology

    J. Alty, G. Amprimo, J. Shin, M. Wuehr, M. Novotny, M. Merello, M. de Koning-Tijssen,, H. Haberfehlner, S. Relton, D. Wong, J. Taeger, A. Zwergal, S. Walther, B. Taati, R. Roemmich, C. Ferraris, M. Mckeown, A. Gupta, R. Li, M. Friedrich (Hobart, Australia)

    Objective: To develop an international consensus framework for clinical video acquisition and metadata reporting optimized for Computer Vision-based movement analysis Background: Advances in Computer Vision (an AI method…
  • 2026 International Congress

    Continued Evaluation of Clinical Outcomes in Participants With Parkinson’s Disease Through 4 Years After Bemdaneprocel Administration

    C. Henchcliffe, H. Sarva, A. Fasano, A. Lozano, S. Kalia, KKH. Yu, C. Brennan, M. Louie-Gao, N. Floro, G. Belfort, V. Tabar (Irvine, USA)

    Objective: To report safety and clinical outcomes in participants with Parkinson’s disease (PD), 4 years after receiving bemdaneprocel. Background: Bemdaneprocel is an investigational cell therapy…
  • 2026 International Congress

    Chronic Vanadium Exposure Promotes Memory Impairment and Aggregation of Alpha-Synuclein, Tau and Amyloid Beta in Mouse Brain

    O. Folarin, F. Olopade, T. Gilbert, A. Ladagu, P. Inês, O. Mustapha, L. Zethan, J. Olopade, T. Outeiro (Ibadan, Nigeria)

    Objective: In this study, we hypothesized that prolonged vanadium exposure may be a potential risk factor for Alzheimer's and Parkinson's diseases. Background: The interaction between…
  • 2026 International Congress

    Sequential neurodegenerative trajectories across the onset of mild parkinsonian signs in isolated REM sleep behavior disorder: a longitudinal multimodal imaging study

    R. Kim, H. Kim, Y. Kim, J. Lee (Seoul, Republic of Korea)

    Objective: To demonstrate the neurodegeneration status implied by mild parkinsonian signs (MPS) in patients with isolated REM sleep behavior disorder (iRBD) by analyzing longitudinal clinical…
  • 2026 International Congress

    Clinicogenetic Characterization of Sporadic Adult-Onset Ataxias in Austria

    L. Schwaighofer, W. Nachbauer, M. Amprosi, D. Boesch, M. Schranz, R. Praschberger, A. Fanciulli, J. Wanschitz, S. Boesch, E. Indelicato (Innsbruck, Austria)

    Objective: To gain insight in the natural history of sporadic adult-onset ataxia (SAOA), identify unrecognized genetic underpinnings and improve early differentiation from other causes of…
  • 2026 International Congress

    Volatile Organic Compound Signatures Differentiate Parkinson Disease from Parkinson Disease Mimic Syndromes and Controls

    A. Dixon, L. Sun, P. Jones, B. Daud Shah, A. Rajput, H. Zhang, E. Noyes (Saskatoon, Canada)

    Objective: We aimed to isolate volatile organic compounds (VOCs) in cerumen and sebum samples from participants with Parkinson disease (PD), PD-mimic syndromes, Idiopathic REM Sleep…
  • 2026 International Congress

    Young-Onset Parkinson’s Disease with Coexisting GBA1 Mutation and ATXN3 Repeat Expansion: A Double Hit?

    D. Yoo, K. Park, T. Ahn (Seoul, Republic of Korea)

    Objective: To report a rare case of young-onset Parkinson’s disease (PD) with a positive family history in which the patient was found to harbor double…
  • 2026 International Congress

    Bayesian Network Analysis of Directional Relationships Among Motor and Non-Motor Symptoms in Parkinson’s Disease

    A. Al-Sharman, H. Khalil, D. Malouche, S. Kanaan, M. Kim, N. Saad, M. Abdelrazeq (Sharjah, United Arab Emirates)

    Objective: To identify directional relationships among motor and non-motor symptoms in people with Parkinson’s disease (PD) using Bayesian Network analysis and to identify central variables…
  • 2026 International Congress

    Identification of Novel FA2H Mutations in Patients with Hereditary Spastic Paraplegia Type 35 (SPG35)

    L. Wang, X. Jin, W. Luo (Hangzhou, China)

    Objective: We reported three cases of SPG35 caused by compound heterozygous mutations in the FA2H gene, with ataxia as the initial clinical manifestation. Among the…
  • 2026 International Congress

    Movement Disorder Phenotypes and Etiological Associations in Genetic Early-Onset Ataxias: A Pediatric Cohort Study

    F. Dridi, H. Klaa, M. Ben Hafsa, Z. Miladi, T. Ben Younes, A. Zioudi, M. Jamoussi, H. Benrhouma, I. Kraoua (Tunis, Tunisia)

    Objective: To investigate the frequency, clinical spectrum, and etiological correlates of movement disorders (MD) in early-onset ataxias. Background: Early-onset ataxias are rare genetic disorders (1).…
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