MDS Abstracts

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

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  • 2025 International Congress

    Compensatory Dynamic Brain Network Mechanisms in Early Lewy Body Dementia: An rs-fMRI Study

    N. Němcová Elfmarková, ľ. Nováková, M. Gajdoš, I. Rektorová (Brno, Czech Republic)

    Objective: To investigate compensatory dynamic brain network mechanisms in early Lewy body dementia (LBD), specifically mild cognitive impairment with Lewy bodies (MCI-LB), using resting-state functional…
  • 2025 International Congress

    Analysis of the Association between SNCA Polymorphisms and the Risk of Multiple System Atrophy

    N. Abramycheva, M. Andreev, L. Karan, I. Minaev, A. Protopopova, A. Protsenko, E. Fedotova, S. Illaroshkin (Moscow, Russian Federation)

    Objective: To assess the impact of twenty-one single nucleotide polymorphisms (SNPs) located in different regulatory regions of the SNCA gene on the risk of developing…
  • 2025 International Congress

    Atypical Parkinsonian Syndromes Presenting with Homonymous Hemianopsia

    T. Le, D. Truong, M. Aung (Houston, USA)

    Objective: We present here two cases of atypical parkinsonism with visual field loss to help increase recognition and drive research efforts forward to elucidate the…
  • 2025 International Congress

    Neurogenic bladder and affective disorders in parkinsonism

    E. Korshunova, M. Khommyatov, M. Samushiya, N. Suponeva (Moscow, Russian Federation)

    Objective: To determine the relationship between psychoemotional and dysuria dysfunctions in patients with PD and MSA. Background: In the group of patients with extrapyramidal pathology…
  • 2025 International Congress

    Expanding the Phenotypic Spectrum of CACNA1A Variants: A Single-Center Experience

    H. Alfaris, S. Yoganathan, P. Jain, M. Moharir, G. Costain, V. Chau, C. Gorodetsky (Toronto, Canada)

    Objective: This study aims to describe pediatric patients with CACNA1A variants, detailing the clinical phenotype, with emphasis on the movement phenomenologies, genetic variants, electrophysiological and…
  • 2025 International Congress

    The Clinicoradiological profile of patients with Osmotic Demyelination Syndrome and Movement Disorders

    D. Dutta, H. Kumar, J. Ganguly, S. Mukherjee (Kolkata, India)

    Objective: This study aims to characterize clinicoradiological features and outcomes in patients of Osmotic Demyelination Syndrome(ODS) presenting with movement disorders(MD). Background: ODS includes central pontine…
  • 2025 International Congress

    Genotype-Phenotype Relations in Neurodegeneration with Brain Iron Accumulation (NBIA) Genes: MDSGene Systematic Review

    N. Reyes, R. Patel, J. Rodriguez-Antiguedad, R. Ramalingam, M. Hamed, A. Duarte, E. Fernandez-Toledo, C. Sun, S. Fereshtehnejad, Y. Mahjoub, M. Emamikhah, S. Camargos, J. Trinh, K. Lohmann, C. Klein, C. Marras, D. Olszewska (Brooklyn, USA)

    Objective: To provide a comprehensive review of individual-level data and genotype-phenotype relationships for genes implicated in neurodegeneration with brain iron accumulation (NBIA) disorders. Background: The…
  • 2025 International Congress

    Examining the Impact of a Single Session of Myofascial Release via Dry Needling on Step Length in Individuals with Parkinson’s Disease

    A. Tahara, A. Gastaldi, A. Chinaglia, V. Tumas, P. Santiago (Ribeirão Preto, Brazil)

    Objective: This study aims to elucidate the impact of a singular myofascial release session employing Dry Needling (DN) on step length within a complete gait…
  • 2025 International Congress

    Prevalence and Comorbidities of Orthostatic Hypotension in Older Adults: A Two-Year Study

    ANA. Ovchynnykova, Y. Trufanov (Kyiv, Ukraine)

    Objective: To determine the prevalence of OH and its associations with autonomic dysfunction, falls, and mortality. Background: Orthostatic hypotension (OH) is a common problem that…
  • 2025 International Congress

    The Role of Mitochondrial DNA Haplogroups in determining the Age of Onset in Indian SCA2 Patients.

    A. Sonakar, C. Sharma, S. Reza, S. Pandey, M. Srivastava, M. Faruq, A. Srivastava (New Delhi, India)

    Objective: To investigate the contribution of mitochondrial DNA (mtDNA) haplogroups to the age at onset (AO) of Spinocerebellar Ataxia type 2 (SCA2) in Indian patients,…
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