MDS Abstracts

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

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  • MDS Virtual Congress 2020

    Functional movement disorder mimicking Parkinson’s disease, a case with supporting evidence

    S. Akbaripanahi, D. Ehrlich (Bethesda, MD, USA)

    Objective: Young onset Parkinson’s disease diagnosis can be challenging, and it is a rare subtype of a disease typically associated with older age. On the…
  • MDS Virtual Congress 2020

    Functional Truncal Orthostatic-Dependent Tremor in A Patient with Autoimmune Thyroid Disorder

    Y. Lin, M.K Lu, B.L Liu, Y.C Chen, C.H Tsai (Taichung, Taiwan)

    Objective: To illustrate the electrophysiological and clinical findings in a patient with functional truncal orthostatic-dependent tremor. Background: Typical orthostatic tremor is a unique type of…
  • MDS Virtual Congress 2020

    Utility Value Analysis For Patients With Essential Tremor Receiving Magnetic-resonance Image-guided Focused Ultrasound Treatment: Three Years Of Follow-Up

    L. Richard, J. Mañez-Miró, W. Ghosh, I. Chatzidaki, B. Ostrander, R. Martínez-Fernández (Tirat Carmel, Israel)

    Objective: To obtain utility values from EQ-5D-3L data of essential tremor (ET) patients receiving magnetic-resonance image-guided focused ultrasound (MRgFUS) and to perform descriptive analyses on…
  • MDS Virtual Congress 2020

    Creating National Competencies in Physical Activity for Exercise Professionals Working with People with Parkinson’s Disease

    L. Hoffman, M. Rafferty (New York, NY, USA)

    Objective: On March 5-6th 2020, the Parkinson’s Foundation is convening a meeting to assemble thought leaders in physical activity and education for Parkinson’s disease.  Our…
  • MDS Virtual Congress 2020

    CAPN1 mutations are more common than expected in patients with hereditary spastic paraparesis

    G. Baille, A. Degardin, I. Strubi-Vuillaume, C. Tard (Lille, France)

    Objective: To report 4 families with hereditary spastic paraparesis due to CAPN1 mutations. Background: Some years ago, CAPN1 mutations have been described as a cause…
  • MDS Virtual Congress 2020

    Novel Mutation in the Protein Kinase C Gamma Gene Causing Spinocerebellar Ataxia-14 in a Large Family

    J. Lahrmann, M. Dagostine, D. Machado (Cheshire, CT, USA)

    Objective: To report a novel mutation not been previously reported in large, multi-ethnic general populations, in the protein kinase C gamma (PRKCG) gene causing spinocerebellar ataxia…
  • MDS Virtual Congress 2020

    Clinical and genetic abnormalities in patients with Friedreich’s ataxia: A genotype-phenotype correlation

    I. Singh, I. Ahmed, S. Shaykya, A. Srivastava (New Delhi, India)

    Objective: To examine the possibility of molecular finding affecting FRDA phenotype, we studied the clinical features and ascertained the GAA repeat sizes in FRDA patients…
  • MDS Virtual Congress 2020

    Case Report: Pseudoatetosis as Manifestation of the Vitamin B12 Deficit

    J. Vargas (Bogotá, Colombia)

    Objective: Subacute combined degeneration (DSAC) of the spinal cord is a classic manifestation in the nervous system of vitamin B12 deficiency, clinically characterized by sensory…
  • MDS Virtual Congress 2020

    Impulsivity and Compulsivity in Cerebellar Ataxias

    N. Amokrane, A. Viswanathan, S. Freedman, C. Yang, S. Kuo, C. Lin (New York, NY, USA)

    Objective: To elucidate the role of human cerebellum in the reward processing system, of which a new cerebellar circuitry was recently identified in mice [1].…
  • MDS Virtual Congress 2020

    Amantadine-induced negative myoclonus in a patient with Parkinson’s disease: A case report

    M. Vuong, L. Poon, A. Lee, J.R Zuzuárregui (San Francisco, CA, USA)

    Objective: To report a case of amantadine-induced negative myoclonus in a patient with Parkinson’s disease. Background: Parkinson’s disease is a progressive neurodegenerative disease that involves…
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