MDS Abstracts

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

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Articles tagged "Magnetic resonance imaging(MRI)"

  • MDS Virtual Congress 2020

    Visualization of Nigrosome 1 at 3T MRI and 18F-DOPA PET for the diagnosis of Parkinson´s disease

    A. Martin-Bastida, V. Suarez-Vega, P. Dominguez-Echavarri, F. Guillen-Valderrama, I. Aviles-Olmos, J. Arbizu, M. Rodriguez-Oroz (Pamplona, Spain)

    Objective: To determine and compare the utility of Nigrosome 1 at 3T MRI and 18F-DOPA PET for the diagnosis of Parkinson´s disease. Background: Differential diagnosis…
  • MDS Virtual Congress 2020

    Regional free-water differentially associated with glial activation, neuroinflammation, and neurodegeneration in de novo Parkinson’s disease

    D. Tosun, R. Ellis (San Francisco, CA, USA)

    Objective: Assess to what extent free-water(FW) as measured by diffusion-weighted MRI(dMRI) is a neuroimaging marker of glial activation, neuroinflammation, and neurodegeneration in de novo Parkinson’s disease(PD) patients from…
  • MDS Virtual Congress 2020

    Cerebellar structural covariance networks in young people with Tourette syndrome

    H. Sigurdsson, S. Jackson, L. Jolley, E. Mitchell, G. Jackson (Nottingham, United Kingdom)

    Objective: To investigate discrete structural brain networks in children and adolescents with Tourette syndrome [TS] relative to a group of matched control participants. Background: TS…
  • 2019 International Congress

    Imaging Parkinson’s disease pathology: A comparison between neuromelanin-sensitive MRI, susceptibility weighted imaging and [11C]PE2I DAT PET

    A. Chandra, G. Pagano, T. Yousaf, H. Wilson, M. Politis (London, United Kingdom)

    Objective: We compared 2 novel MRI techniques: neuromelanin-sensitive MRI (NM-MRI) and susceptibility weighted imaging (SWI) with [11C]PE2I PET in order to establish their validity as biomarkers…
  • 2019 International Congress

    Braak model in Parkinson disease using MRI biomarkers

    N. Pyatigorskaya, L. Yahia-Cherif, R. Valabregue, R. Gaurav, M. Mongin, C. Ewenczyk, C. Gallea, F. Gargouri, E. Bardinet, I. Arnulf, M. Vidailhet, S. Lehericy (Paris, France)

    Objective: The aim of this study was to test using multimodal MRI biomarkers if the pattern of neurodegeneration in the brain of patients with PD…
  • 2019 International Congress

    MCI reverters have a favorable cognitive prognosis and cortical integrity in Parkinson’s disease

    SJ. Chung, Y-H. Park, YH. Sohn, J-M. Lee, PH. Lee (Seoul, Republic of Korea)

    Objective: To investigate whether reversion to cognitively normal status (CogN) is clinically relevant in Parkinson’s disease with mild cognitive impairment (PD-MCI). Background: The concept of…
  • 2019 International Congress

    Structural connectome of brainstem nuclei in REM sleep behavior disorder, a model of premanifest synucleinopathy

    MG. García-Gomar, LD. Lewis, L. Wald, B. Rosen, A. Videnovic, M. Bianciardi (Boston, MA, USA)

    Objective: To investigate in vivobrainstem structural connectivity changes in a model of premanifest synucleinopathy, REM sleep behavior disorder (RBD), using 7 T high spatial-resolution diffusion-tensor-imaging (DTI)…
  • 2019 International Congress

    Longitudinal Analysis of the Corticospinal tract microstructure in Parkinson’s Disease Patients

    R. Guimarães, L. Piovesana, P. Azevedo, B. Campos, F. Cendes (Campinas, Brazil)

    Objective: To assess longitudinal abnormlities throughout  the corticospinal tract in Parkinson’s Disease patients. Background: Parkinson’s Disease (PD) is a neurodegenerative progressive disease might become a pandemic…
  • 2019 International Congress

    Structural imaging changes in hepatic and neurological Wilson disease

    A. Patel, K. Nalamada, A. Vives-Rodriguez, D. Robakis, T. Constable, J. Arora, M. Schilsky, S. Tinaz (New Haven, CT, USA)

    Objective: To quantitatively assess cerebral structural changes in Wilson disease (WD) subjects with hepatic and neurological phenotypes. Background: WD is a rare autosomal recessive disorder…
  • 2019 International Congress

    Heterozygous DCC mutations, more than congenital mirror movements

    S. Thams, M. Islam, M. Lindefeldt, A. Nordgren, T. Granberg, D. Nilsson, M. Paucar (Stockholm, Sweden)

    Objective: To perform a comprehensive characterization of 5 patients with variable degree of congenital mirror movements. Background: Congenital mirror movements (CMM) are rare non-progressive syndromes…
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