MDS Abstracts

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

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  • 2017 International Congress

    Objective measurement of upper extremity bradykinesia using the keyboard-based dexterity test

    S.-k. Song, J.-H. Kang (Jejusi, Republic of Korea)

    Objective: To objectively assess the bradykinesia of upper extremity using the Objective Movement Disorder Measurement (OMDM)-Dexterity test Background: Bradykinesia is one of the clinical hallmarks…
  • 2017 International Congress

    Beyond shuffling: Gait phenotypes in Parkinson’s Disease

    L. Solis-Cohen, C. Ashton, D. Simon, M. Fox, D. Tarsy, R. Alterman, V. Vanderhorst, L. Shih (Boston, MA, USA)

    Objective: To describe commonly observed gait phenotypes in a cohort of advanced Parkinson's Disease (PD) patients. Background: Gait disorders in PD are varied and complex.  Even…
  • 2017 International Congress

    The 3-step clinical prediction tool for falls in Parkinson’s disease: can it be used as a self-assessment measure?

    L. Mewburn, N. Allen, R. Adams, C. Canning (Lidcombe, Sydney, Australia)

    Objective: To determine if people with Parkinson’s disease (PD) are able to estimate their gait speed relative to a threshold speed of 1.1 m/s. Background:…
  • 2017 International Congress

    Lateralization of fine motor actions in Tourette syndrome persisting through adulthood

    D. Martino, C. Delorme, E. Pelosin, A. Hartmann, Y. Worbe, L. Avanzino (Calgary, AB, Canada)

    Objective: To evaluate whether decreased lateralization of fine motor actions is an endophenotypic trait in adults with Tourette syndrome (TS), and whether it is related…
  • 2017 International Congress

    Rehabilitation program with or without a whey protein-based nutritional support enriched with essential aminoacids and vitamin D in patients with Parkinson’s disease or parkinsonism: study design of a randomized, controlled trial.

    m. barichella, E. Cereda, G. Pinelli, l. Iorio, V. Ferri, g. Frazzitta, E. Cassani, G. Riboldazzi, G. Pezzoli (Milano, Italy)

    Objective: Objective. To evaluate whether the use of a whey protein-based nutritional formula enriched with essential aminoacids – particularly leucine - and vitamin D have…
  • 2017 International Congress

    Noninvasive cerebellar stimulation for adults with cervical dystonia

    A. McCambridge (Sydney, Australia)

    Objective: To examine whether a 5 day treatment period of anodal transcranial direct current stimulation (a-tDCS) over the cerebellum would improve patients’ symptoms and alter…
  • 2017 International Congress

    History and Management of Status Dystonicus

    E. Nerrant, V. GONZALEZ, C. MILESI, T. Roujeau, E. Chan Seng, F. Cyprien, G. Cambonie, P. Coubes, L. CIF (Montpellier, France)

    Objective: To describe a consecutive series of 40 status dystonicus patients, identify major clinical characteristics and to document medical and surgical management. Background: Characteristics and evolution…
  • 2017 International Congress

    Brain volume changes in relation to intracortical inhibition and clinical benefit of pallidal stimulation in dystonia: a combined VBM and TMS study.

    R. Jech, A. Fečíková, V. Čejka, V. Čapek, D. Šťastná, F. Růžička, D. Urgošík, E. Růžička (Prague, Czech Republic)

    Objective: To explore the relationship between brain morphology, clinical effects of bilateral pallidal stimulation (GPi DBS) and intracortical inhibition of the motor cortex in patients…
  • 2017 International Congress

    Self-assessed psychological symptoms, fatigue and depersonalization in dystonia

    R. Newby, J. Alty, S. Jamieson, S. Smith, P. Kempster (Melbourne, Australia)

    Objective: To assess depressive, anxiety, fatigue and dissociative symptoms in patients with dystonia. Background: The basal ganglia, once considered exclusively concerned with motor control, are…
  • 2017 International Congress

    Focal dystonia as an early symptom of CACNA1A mutation: case report and literature review.

    Y. Gu, K. Kumar, C. Sue (Sydney, Australia)

    Objective: We describe two cases, a father-daughter pair, of CACNA1A mutation with task specific dystonia as an early feature. The father otherwise had a phenotype…
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