MDS Abstracts

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

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  • 2018 International Congress

    Impact of electrode impedance changes in clinical outcomes of patients with Parkinson’s disease and subthalamic nucleus deep brain stimulation

    ME. Contreras Pinto, J. Martins, C. Cerquera, S. Dias, D. Giraldo Salazar, JS. Saavedra Moreno, F. Vallderiola Serra (La Serena, Chile)

    Objective: To assess the longitudinal changes in impedance values of CV neurostimulation devices and its possible impact in the clinical outcome of PD patients with…
  • 2018 International Congress

    Deep brain stimulation in Parkinson’s disease: From the stimulation of a nucleus to the stimulation of neuronal networks

    A. Arévalo, L. López Manzanares, R. Manzanares, M.A. García-Pallero, M. Navas, P. Pastor, L. Vega Zelaya, CV. Torres Diaz. (Madrid, Spain)

    Objective: To evaluate global changes in connectivity of large-scale structural brain networks in Parkinson's disease (PD) patients, and to test the hypothesis that deep brain…
  • 2018 International Congress

    Clinical and morphometric features of the tics

    S. Munasipova, Z. Zalyalova (Kazan, Russian Federation)

    Objective: To evaluate clinical and morphometric features in patients with tics in association with OCD and ADHD Background: In recent years there have been reports…
  • 2018 International Congress

    Hearing Evaluation (Peripheral and Central) in Patients with Sporadic Ataxia

    H. Teive, B. Zeigelboim, A. Vom Scheidt, K. Kronbauer, N. Mello, R. Santos (Curitiba, Brazil)

    Objective: To describe the audiological and electrophysiological results in patients with sporadic ataxia. Background: Patients with progressive non-familial adult ataxia are classified into a sporadic…
  • 2018 International Congress

    Clinico-genetic correlation in Indian Spinocerebellar ataxia Type 1 (SCA1) patients

    A. Takkar, I. Ahmed, S. Shakya, A. Srivastava (New Delhi, India)

    Objective: To conduct a clinical and genetic analysis of SCA 1 in Indian population. Background: Spinocerebellar ataxia type1 (SCA1) is a neurodegenerative disease caused by…
  • 2018 International Congress

    Coexisting CACNA1A pathogenic variant and MJD expansion in the same family

    L. Leitão, C. Figueiredo, M. Santos, A.F. Brandão, A. Lopes, J. Sequeiros, I. Alonso, C. Costa (Amadora, Portugal)

    Objective: Genetic investigation of a family with inherited cerebellar ataxia. Background: Despite the identification of an increasing number of genes causing dominant spinocerebellar ataxias (SCAs),…
  • 2018 International Congress

    Rapidly progressive ataxia caused by an undetermined paraneoplastic disorder: A case report

    J. Conway, A. Feigin (New York, NY, USA)

    Objective: To report the case of a 69-year-old woman with rapidly progressive ataxia. Background: Various cases exist in the literature of rapidly progressive ataxia secondary…
  • 2018 International Congress

    Two cases of hemichorea-hemiballism in nonketotic hyperglycemia

    S.H. Yi, H.Y. Park (Iksan, Republic of Korea)

    Objective: We describe two cases of Hemichorea-Hemiballism (HCHB) associated with nonketotic hyperglycemia. Background: HCHB is defined as continuous, non-patterned, and involuntary movement involving one side…
  • 2018 International Congress

    The clinical value of SPECT in identifying dystonic muscles of patients with cervical dystonia

    L. Jin, L. Feng, I. Djibo, S. Chen, F. Teng, B. Li, H. Ma (Shanghai, China)

    Objective: The aim of this study is to compare the efficacy of selecting target muscles for botulinum toxin injection by abnormal movement pattern and by…
  • 2018 International Congress

    Siblings with a PRKRA (DYT16) Mutation and Startle Myoclonus

    L. Wiblin, M. Baker, M. Lai, R. Horvath, N. Warren (Newcastle upon Tyne, United Kingdom)

    Objective: To characterize and expand the phenotype of a family from North-East England with DYT16. Background: DYT16 is an autosomal recessive disease associated with mutations…
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