MDS Abstracts

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

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  • 2025 International Congress

    Whispers of Hope Motor and Psychiatric Recovery in Fahr’s Disease with High-Frequency rTMS: A Case Report

    D. Ortiz-Zacarias, JA. Sánchez Garza, S. Luna Garza, N. Gutierrez Canales, V. Medina Mier, S. Castillo-Torres, IE. Estrada-Bellman (Monterrey, Mexico)

    Objective: To present a case of FD showing significant motor and psychiatric improvement following high-frequency rTMS of the DLPFC Background: Fahr’s disease (FD) is a…
  • 2025 International Congress

    Diagnostic mismatches between clinical assessment, imaging and alpha-synuclein biomarkers in parkinsonian syndromes

    A. Gomez, C. Malatt, E. Hogg, E. Tan, Y. Bordelon, B. Frommel, M. Tagliati (Los Angeles, USA)

    Objective: To analyze the frequency of matching information provided by traditional clinical assessment, dopamine transporter (DaTscan), and skin biopsy results in patients with undiagnosed parkinsonian syndromes. Background:…
  • 2025 International Congress

    Rapid Onset Progressive Dystonia with Parkinsonism

    D. Nguyen, R. Parihar (Bronx, USA)

    Objective: To illustrate a case of a patient presenting with oromandibular dystonia with blepharospasm (Meige syndrome) and progressing to a segmental dystonia with parkinsonism. This…
  • 2025 International Congress

    Comparison of Prodromal Features between Parkinson’s Disease and Dementia with Lewy Bodies over 15 Years

    G. Scott, S. Karki, J. Quinn, L. Neilson (Portland, USA)

    Objective: Compare the association of classic prodromal features with subsequent development of Parkinson’s Disease (PD) versus Dementia with Lewy Bodies (DLB). Background: DLB shares pathology…
  • 2025 International Congress

    MicroRNA Landscape of Multiple System Atrophy: Insights from Plasma and Patient-Derived Induced Pluripotent Stem Cell Models

    K. Kuo, C. Chen, L. Lin, W. Wu (Taipei, Taiwan)

    Objective: To identify small non-coding RNAs (sncRNAs) signatures in multiple system atrophy (MSA) and elucidate their functional mechanisms within patient-derived induced pluripotent stem cell-differentiated oligodendrocytes…
  • 2025 International Congress

    Cutaneous Phosphorylated Alpha-Synuclein Deposition in Multiple System Atrophy

    R. Freeman, T. Levine, B. Bellaire, C. Gibbons (boston, USA)

    Objective: To report differences in the amount, localization and topographic distribution of cutaneous P-SYN deposition between cerebellar and parkinsonian variants of MSA. Background: MSA is…
  • 2025 International Congress

    Connectome of Pathology Stages of Progressive Supranuclear Palsy

    N. Vallenas, H. Tanaka, S. Lee, G. Kovacs, B. Couto (New York, USA)

    Objective: Find the relations between normative FC and seed-to-seed correlations in pathological tau load. Model the FC maps for twelve patients, using post-mortem tau pathology…
  • 2025 International Congress

    Absence of identifiable neuropathological correlates of cognitive impairment in multiple system atrophy

    S. Radmard, T. Ma, J. Agin-Liebes (Atlanta, USA)

    Objective: To analyze neuropathological correlates of cognitive impairment in multiple system atrophy (MSA) and characterize the affected cognitive domains. Background: Current MSA census criteria delineate…
  • 2025 International Congress

    Atypical Parkinsonism with LRRK2 Mutation Presenting as Multiple System Atrophy

    K. Makhoul, R. Ramdhani (Great neck, USA)

    Objective: We describe a rare case of atypical parkinsonism associated with leucine-rich repeat kinase 2 (LRRK2) gene mutation presenting with clinical features suggestive of multiple…
  • 2025 International Congress

    Characterizing the Patient Clinical Journey Before and After Diagnosis of Friedreich Ataxia and Differences by Age at Diagnosis

    A. Henriquez, M. Hatcher, B. Bian, A. Didonato, S. England, Q. Ip, X. Ma, J. Mckay, R. Avila (Seattle, USA)

    Objective: To characterize the patient journey through clinical specialties involved in the intermediate-to-late age at diagnosis of adult patients with Friedreich ataxia (FA) based on…
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