MDS Abstracts

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

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2024 International Congress

September 27-October 1, 2024. Philadelphia, PA.

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  • A Nomogram Model for Predicting Malnutrition among Patients with Parkinson’s Disease

    Q. Huang, X. Zou (Chengdu, China)

  • A non-linear index can detect early postural instability in people with Parkinson’s disease: Enhancing perspectives on the utilization of cost-effective technologies.

    G. Santos, M. D'Alencar, A. Frazão, A. Roque, J. Vivas, M. Piemonte (São Paulo, Brazil)

  • A novel G413S mutation in the CSF1R gene causes Hereditary Diffuse Leucoencephalopathy with axonal Spheroids; clinically overlapping features of Parkinsonism

    ANW. Ullah, MZB. Badshah (Peshawar, Nepal)

  • A Novel Mutation of NKX2-1 Gene: A Rare Presentation of Chorea

    BC. Ari, S. Canbek, G. Kenangil (ISTANBUL, Turkey)

  • A Novel Peer Mentoring Support System for Persons with Parkinson’s Disease

    E. Lubas, TW. Liang, K. Stoveld, SK. Thurman (Philadelphia, USA)

  • A novel single-cell reporter identifies regulators of the endogenous PINK1-Parkin mitochondrial quality control pathway

    J. Thayer, X. Huang, J. Hawrot, D. Ramos, M. Ward, D. Narendra (BETHESDA, USA)

  • A Novel SLC9A1 Mutation Associated with Cerebellar Ataxia and Sensorineural Hearing Loss

    S. Dharmadhikari, Y. Kianirad (Chicago, USA)

  • A pathology-validated study to investigate the role of Uric Acid in Parkinson’s Disease

    P. Pecoraro, S. Carbone, V. Di Lazzaro, L. Di Biase (Rome, Italy)

  • A Patient with Overlapping SPG7 mutation and MERRF

    J. Patino, M. Koenig (Houston, USA)

  • A Phase 1b Randomized, Placebo-Controlled, Delayed-Start Trial of UB-312 in Synucleinopathies.

    P. Millar Vernetti, D. Mirski, JC. Dodart, A. Wood, HJ. Yu, J. Boyd, P. Kundu, R. Setton, D. Silbersweig, E. Stern, C. Lucero, S. Gerrol, H. Kaufmann, J. Martinez (New York, USA)

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