MDS Abstracts

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

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Articles tagged "Aging"

  • 2025 International Congress

    Epigenome-wide and gene-targeted epigenetic profile of isolated REM Sleep Behaviour Disorder: a clinico-molecular study

    L. Baldelli, C. Pirazzini, L. Sambati, F. Ravaioli, F. Di Laudo, D. Gentilini, P. Guaraldi, C. Franceschi, P. Cortelli, P. Garagnani, G. Calandra-Buonaura, MG. Bacalini, F. Provini (Bologna, Italy)

    Objective: Comprehensively characterize the epigenetic profile of isolated REM Sleep Behaviour Disorder (iRBD) using genome-wide and gene-targeted approaches, linking it to clinical measures and  phenoconversion.…
  • 2025 International Congress

    Role of APOE Polymorphism and CSF Markers of AD Co-Pathology in the Cognitive Trajectories of Sporadic and Genetic Parkinson’s Disease: A Longitudinal Cohort Study

    R. Botta, J. Locascio, R. Ye, A. Goodheart, S. Gomperts (Boston, USA)

    Objective: To evaluate if APOE genotype and CSF biomarkers of AD co-pathology are associated with distinct rates of cognitive decline in PD subtypes. Background: Cognitive…
  • 2025 International Congress

    Comparison of clinical symptoms between young-onset and elderly-onset in patient with early Parkinson’s disease

    M. Iijima, R. Morimoto, K. Suzuki, S. Nogawa, Y. Okuma (Tokyo, Japan)

    Objective: We compared the clinical symptoms of early Parkinson's disease (PD) between young-onset and elderly-onset. Background: The progression of PD varies depending on the age…
  • 2025 International Congress

    Epidemiology of Parkinson’s disease in Southern Brazil: Age- and Sex-Specific Findings from the PROBE-PD Study

    G. Pereira, N. Soares, C. Sangali, D. Teixeira-Dos-Santos, G. Valença, B. Lopes, P. Brandão, C. Rieder, A. Schuh (Porto Alegre, Brazil)

    Objective: To examine the prevalence of Parkinson’s disease and parkinsonism in individuals aged 60 years and older in a population-based sample from Southern Brazil, analyzing…
  • 2025 International Congress

    Planning for the Parkinson’s Pandemic: Care needs in Australian Residential Aged Care Facilities

    J. Mcginley, S. Soh, Y. Mok, M. Callisaya, V. Mcconvey, M. Klaic, A. Vogel, D. Koye, D. Finkelstein, K. Bower (Parkville, Australia)

    Objective: To evaluate the prevalence, demographic characteristics and care needs of people with Parkinson’s disease (PD) living permanently in residential aged care facilities (RACF) in…
  • 2025 International Congress

    Ecologically Valid, Ambient, Longitudinal, and Unbiased Assessment of Treatment Efficacy in Parkinson’s Disease (EVALUATE-PD)

    J. Kaye, E. Leonard, L. Talman, N. Rodrigues, Z. Beattie (Portland, USA)

    Objective: To determine the feasibility of using in-home digital biomarkers (DBs) and activity monitoring for clinical trials and studies of early Parkinson’s Disease (PD) and…
  • 2025 International Congress

    Impact of Innovative Physiotherapy Interventions on Motor Function and Quality of Life in Patients with Parkinson’s Disease and Movement Disorders

    E. Nakanwagi, G. Wangolo (KAMPALA, Uganda)

    Objective: 1. Assess the extent to which innovative physiotherapy interventions improve motor function, as measured by the Unified Parkinson’s Disease Rating Scale (UPDRS).2. Determine the…
  • 2025 International Congress

    Breaking Away From the Ivory Tower

    J. de (Kogarah, Australia)

    Objective: We describe the evolution of the Geriatric Flying Squad (GFS), a rapid response outreach team for residential aged care facilities (RACFs) in the local…
  • 2025 International Congress

    A Long-Living Human Tissue Engineered Nigrostriatal Pathway as a Testbed to Study Parkinson’s Disease

    D. Chouhan, A. Bello, K. Cullen, J. Duda (Philadelphia, USA)

    Objective: To create a three dimensional (3D) long-living model of human tissue-engineered nigrostriatal pathway (TE-NSP) comprised of discrete somatic and axonal compartments recapitulating the native…
  • 2025 International Congress

    Detection and characterization of rare variants in NOTCH2NLC causing false negative molecular diagnosis through long-read sequencing

    N. Jin, X. Zheng, W. Luo (Hangzhou, China)

    Objective: This study investigated a NIID patient with typical clinical and imaging features but no detectable NOTCH2NLC GGC expansion using standard testing. Whole-genome long-read sequencing…
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