MDS Abstracts

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

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Articles tagged "Parkinsonism"

  • 2025 International Congress

    Role of presenilin 1 variants in parkinsonism

    M. Kinoshita, H. Ohara, R. Sasaki, K. Tamura, A. Elangovan, HW. Suresh Babu, S. Muthukumar, M. Iyer, B. Vellingiri (Kyoto, Japan)

    Objective: To characterize presenilin 1 gene (PSEN1) variants which can cause parkinsonism. Background: Variants in PSEN1 are associated with early onset Alzheimer’s disease mainly due…
  • 2025 International Congress

    Parkinsonism after Post-Anoxic Brain Injury

    B. Petko, S. Factor, R. Tripathi (Atlanta, USA)

    Objective: To describe two cases of parkinsonism caused by anoxic brain injury. Background: Movement disorders occur in about 40% of patients following anoxic brain injury,…
  • 2025 International Congress

    Atypical Frontotemporal Dementia with Parkinsonism Linked to SQSTM1 Mutation A Clinicopathological Case Study

    C. Espinoza Vinces, M. Zelaya Huerta, V. Coca Pueyo, G. Montoya Murillo, A. Patiño García, R. Villino Rodríguez, A. Atorrasagasti Villar, J. Arbizu, M. Riverol (Pamplona, Spain)

    Objective: To describe the clinical, neuroimaging, and neuropathological features of a patient with frontotemporal dementia (FTD) and parkinsonism related to mutation in the SQSTM1 gene.…
  • 2025 International Congress

    Multiscale entropy: a New Oculomotor Measure of PSP.

    C. O'Keeffe, A. Gallagher, J. Inocentes, B. Coe, B. White, D. Brien, D. Munoz, R. Walsh, T. Lynch, C. Fearon (Dublin, Ireland)

    Objective: The objective of this study was investigate whether multiscale entropy, a measure of complexity, when applied to the path of unconstrained eye movements could…
  • 2025 International Congress

    Conjugal Parkinsonism

    CK. Tan (Singapore, Singapore)

    Objective: To report a case of multiple system atrophy (MSA) and progressive supranuclear palsy (PSP) in a couple. Background: Conjugal parkinsonism denotes an entity where…
  • 2025 International Congress

    Wearable Sensor-Based Assessment of Lower Extremity Dystonia in X-linked Dystonia Parkinsonism

    G. Corniani, N. Landra, N. Ganza, S. Begalan, P. Acuna, C. Go, S. Baker, N. Sharma, P. Bonato, C. Stephen (Boston, USA)

    Objective: To develop a sensor-based pipeline to identify lower limb dystonic features in X-linked dystonia parkinsonism (XDP). Background: XDP is a rare neurogenetic combined movement…
  • 2025 International Congress

    Identifying the Prognostic Outcomes of Parkinson’s Patients with Impaired Swallow.

    J. Acharya, J. Dols, A. Lingeswaran, A. Aranda-Martinez, A. Manzoor, K. Yeong, C. Chikusu, P. Enwere, R. Lisk, K. Soliman, R. Williams, E. Wilkinson (Chertsey, United Kingdom)

    Objective: To identify the prognostic outcomes of patients with Parkinson’s disease (PD) when they are unable to take their oral medication and are medicated via…
  • 2025 International Congress

    Balance biomarker for early differentiation of Parkinson’s disease and multiple system atrophy with parkinsonian type

    HJ. Chang, JH. Kim, S. Lee, E. Kwon, SH. Jeong, E. Oh (Daejeon, Republic of Korea)

    Objective: We propose a random forest model utilizing balance analysis to differentiate early-stage Parkinson’s disease (PD) and multiple system atrophy with parkinsonian type (MSA-P) patients.…
  • 2025 International Congress

    The Role of Cognitive Impairment in the Effectiveness of Rehabilitation Training Programs for Parkinson’s Disease: A Review of Current Evidence

    A. Elsayed, Z. Hegazy, K. Ahmed, O. Sabry, S. Elsenbawy, G. Abozeid, M. M. Elsayed (Mansoura, Egypt)

    Objective: To examine the impact of cognitive impairment (CI) on the effectiveness of rehabilitation training programs in individuals with Parkinson’s disease (PD) and identify strategies…
  • 2025 International Congress

    Analysis showed resemblance in Genetic architecture of rare movement disorders in consanguineous Pashtoon ethnic group

    S. Rehman (Bannu, Pakistan)

    Objective: Present Study was focused on improving the available genetic architecture of rare movement disorders (MD) and subsequent use of this knowledge for protective measurements…
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