MDS Abstracts

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

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Articles tagged "Dystonia: Pathophysiology"

  • 2019 International Congress

    Features of neural activity of globus pallidus in a patient with cervical dystonia and putaminal stroke: case study

    A. Gamaleya, A. Tomskiy, S. Usova, V. Popov, AG. Shaikh, A. Sedov (Moscow, Russian Federation)

    Objective: To describe single unit neural activity in globus pallidus (GP) of cervical dystonia (CD) patient with putaminal stroke and compare it with CD patients…
  • 2019 International Congress

    Smell and taste in cervical dystonia: a contribution to understand dystonia pathophysiology.

    T. Herr, T. Hummel, M. Vollmer, C. Willert, B. Lehnert, M. Kronenbürger (Greifswald, Germany)

    Objective: To contribute to the better understanding of the pathophysiology of cervical dystonia (CD) we systematically assessed olfactory and gustatory functioning in CD subjects and…
  • 2019 International Congress

    Abnormal Sensorimotor Processing in Cervical Dystonia in Functional Magnetic Resonance Imaging

    L. Hvizdosova, P. Hok, D. Lachmanova, M. Nevrly, P. Otruba, P. Hlustik, P. Kanovsky (Olomouc, Czech Republic)

    Objective: The aim of this study was to assess brain activation during voluntary sequential finger tapping in cervical dystonia patients while manipulating task complexity. Background: Cervical dystonia…
  • 2019 International Congress

    Defective human motion perception in cervical dystonia correlates with coexisting tremor

    D. Martino, E. Pelosin, G. Abbruzzese, L. Avanzino (Genova, Italy)

    Objective: To evaluate whether perceptual encoding of body motion in cervical dystonia (CD) is associated with co-existing tremor. Background: Patients with focal CD or hand…
  • 2019 International Congress

    Interactions within Fine Motor Control Network in Task-specific Dystonia

    S. Merchant, E. Frangos, S. Horovitz, T. Popa, J. Parker, M. Hallett (Charleston, SC, USA)

    Objective: Using a novel methodology combining neuroimaging and transcranial magnetic stimulation(TMS), we explored the difference in the interactions between the principal nodes of the fine…
  • 2019 International Congress

    Evaluating Multimodal Integration of Abnormalities in Adult Onset Idiopathic Focal Dystonia (AOIFD) via Multivariate Pattern Analysis (MVPA) and Ensemble Learning (EL)

    S. Narasimham, D. Valeriani, S. O'Riordan, M. Hutchinson, K. Simonyan, R. Reilly (Dublin, Ireland)

    Objective: Investigate MVPA and EL for understanding the relationship between structural and functional abnormalities in AOIFD. Background: AOIFD is a movement disorder with diverse phenotypes…
  • 2019 International Congress

    Trust the Patient’s Report, not the Doctor’s: Non-Motor Symptoms and Quality of Life in Cervical Dystonia

    I. Ndukwe, J. Dover, P. Lynch, C. O'Neill, S. O'Riordan, M. Hutchinson (Dublin, Ireland)

    Objective: To assess the prevalence of mood disorder and measure health-related quality of life (Hr-QoL) in relation to, pain, disability and disease severity in cervical…
  • 2019 International Congress

    A software framework for objective and quantitative audio-analysis of Embouchure Dystonia (ED)

    M. Perez Denia, O. Killian, I. Ndukwe, S. Narasimham, S. O’Riordan, M. Hutchinson, R. B. Reilly (Dublin, Ireland)

    Objective: Development of an automated audio-analysis software framework for aiding in biomarker identification to objectively quantify ED severity. Background: ED, the second most common phenotype…
  • 2019 International Congress

    The Sequelae of Kernicterus

    Z. Aldaajani, E. Ali (Dhahran, Saudi Arabia)

    Objective: To highlight the long- term sequelae of Kernicterus Background: Kernicterus refers to the clinical features of chronic bilirubin encephalopathy which if not treated can…
  • 2019 International Congress

    Nigrostriatal degeneration in DYT-PRKRA: new insights on a rare disorder

    MJ. Pinto, J. Massano, MJ. Rosas, A. Oliveira (Porto, Portugal)

    Objective: To describe a genetically proven DYT-PRKRA (DYT16) case with documented loss of presynaptic dopamine transporters. Background: DYT-PRKRA is an autosomal recessive disorder combining generalized…
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