MDS Abstracts

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

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Articles tagged "Huntingtons disease"

  • 2019 International Congress

    Jane Avril: Toulouse-Lautrec’s favourite courtisan and Moulin Rouge’s choreic dancer

    F. Germiniani, C. Camargo, G. Franklin, G. Ribas, L. Pinheiro, P. Marques, H. Teive (Curitiba, Brazil)

    Objective: Our aim is to analyse selected portraits of Jane Avril, Moulin Rouge's most famous dancer, done by Toulouse-Lautrec, in which some features of chorea…
  • 2019 International Congress

    Neurology Residents Versus a Mobile Medical Application in deducing differential diagnoses in Movement Disorders: A multi-center, cross-sectional, observational study

    V. Vishnu, P. Vinny, R. Rajan, V. Goyal, P. Srivastava, V. Lal, P. Sylaja, L. Narasimhan, S. Dwivedi, P. Nair, D. Ramachandran, A. Gupta (New Delhi, India)

    Objective: To test the hypothesis that the differentials generated by the  Mobile Medical Application  are more clinically relevant and complete to the ones derived by…
  • 2019 International Congress

    Management of life threatening dyskinesias in GNAO1 related movement disorder: two new cases and review of the literature

    M. Hull, M. Parnes (Houston, TX, USA)

    Objective: To present two cases of GNAO1 related movement disorder associated with life threatening persistent chorea successfully managed with bilateral GPi deep brain stimulation (GPi-DBS)…
  • 2019 International Congress

    Pediatric anti-N-methyl-D-aspartate receptor encephalitis associated with Coat’s-like retinal telangiectasia

    N. Kumar, D. Radhakrishnana, R. Shree, G. Madhaw, R. Samanta, S. Kumari (Rishikesh, India)

    Objective: We report a case of 5-year-old Indian boy with non-paraneoplastic anti NMDAR encephalitis associated with Coat's like retinal telangiectasia. Background: Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis…
  • 2019 International Congress

    Novel compound heterozygous mutations in the TSFM gene causes childhood-onset chorea

    CH. van Riesen, K. von Au, S. Biskup, A. Kühn, A. Kaindl, A. van Riesen (Berlin, Germany)

    Objective: To report the case of a young boy suffering from a severe hyperkinetic movement disorder caused by mutations in the recently described TSFM gene.…
  • 2017 International Congress

    Examining central cognitive processing speed as an early marker of Huntington’s disease (HD) onset

    A. Nathan, S. Park, P. Gilbert, J. Corey-Bloom (La Jolla, CA, USA)

    Objective: To examine central processing speed as an early marker of Huntington’s disease (HD) onset using the Computerized Test of Information Processing (CTiP). Background: The CTiP,…
  • 2017 International Congress

    Inhibiting sphingosine-1-phosphate lyase as a possible therapy in Huntington’s disease

    E. Furr Stimming, J.F. Manchon, A. Tsvetkov (Houston, TX, USA)

    Objective:  To advance our understanding of the process by which the mutant huntingtin (mHTT) protein contributes to neurodegeneration and translate that knowledge to potentially effective disease…
  • 2017 International Congress

    Evidence of putaminal petechial hemorrhage as the cause of hyperglycemic chorea

    J.-J. Lin (Nantou, Taiwan)

    Objective: To report a series of magnetic resonance image (MRI) study and advise the initial putaminal petechial hemorrhage following with gliosis as the cause of…
  • 2017 International Congress

    Salivary biomarkers for Huntington’s disease (HD)

    J. Corey-Bloom, A. Aikin, S. Park, A. Haque, A. Nathan, D. Granger, S. Granger, E. Thomas (La Jolla, CA, USA)

    Objective: The objective of the current study was to assess the potential for saliva to serve as a biospecimen for accessible biomarkers for Huntington’s disease…
  • 2017 International Congress

    Dynamic prediction of motor diagnosis in Huntington’s disease using a joint modeling approach

    K. Li, E. Furr Stimming, S. Luo, K. Li (Houston, TX, USA)

    Objective: Compare various clinical and biomarker trajectories for tracking Huntington's disease (HD) progression and predicting motor conversion. Background: Huntington’s disease (HD) is a fatal neurodegenerative disease…
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