MDS Abstracts

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

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2023 International Congress

August 27-31, 2023. Copenhagen, Denmark.

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  • Case report- Cavernoma involving substantia nigra and nigrostriatal pathway as a rare cause of secondary parkinsonism with a 3 year follow up

    S. Sathyanarayana, J. Pasquini, D. Ledingham, D. Mitra, N. Warren, N. Pavese (Newcastle Upon Tyne, United Kingdom)

  • Case Report: Supranuclear Palsy and Increased Intraocular Pressure in Normal Pressure Hydrocephalus

    K. Young, M. Gates (Austell, USA)

  • Case series of Steroid-responsive Encephalopathy Associated with Autoimmune Thyroiditis (SREAT); different presentations and different treatment outcomes.

    K. Methawasin, M. Jaisa-Aad (Nakhon Nayok, Thailand)

  • Case Study: Pitfalls of Commercial Genetic Testing for Huntington’s Disease

    L. Fanty, J. Bravo, S. Corrigan, M. Maczis, L. Kugelmann, A. Wagle Shukla, M. Farrer, N. Mcfarland (Gainesville, USA)

  • Caveats regarding a family with PD and LRRK2 mutations

    P. Ferreira, A. Ferreira, D. Fitas, S. Moreira, M. Calejo (Senhora da Hora, Portugal)

  • CBS presenting rapidly progressive anterior operculum syndrome with suggested background pathology of 4-repeat tauopathy by tau PET: A case report

    K. Nakamura, Y. Kuroha, M. Hatakeyama, A. Kimura, Y. Nakamura, Y. Murakami, M. Watanabe, H. Igarashi, T. Takahashi, H. Shimada (Niigata city, Japan)

  • Cell-specific MAPT gene expression is preserved in tau cytopathologies in Progressive Supranuclear Palsy

    S. Forrest, S. Lee, N. Nassir, V. Sackmann, I. Martinez-Valbuena1, J. Li, A. Ahmed, L. Ittner, A. Lang, M. Uddin, G. Kovacs (Toronto, Canada)

  • Cerebellar ataxia as primary manifestation of HIV: a rare etiological association

    S. Jain, PN. Renjen, M. Gupta, P. Agarwal (Jaipur, India)

  • Cerebellar ataxia due to vitamin E deficiency

    N. Stojiljkovic, S. Redko, F. Gupta, S. Kathiresu Nageshwaran, W. Tse (New York, USA)

  • Cerebellar ataxia in Hypomyelinating Leukodystrophies: A case series

    J. Ganguly, J. Sinha, P. Basu, M. Tiwari, H. Kumar (Kolkata, India)

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