MDS Abstracts

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

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Articles tagged "Iron"

  • 2018 International Congress

    Plasma transferrin level correlates with the tremor-dominant phenotype of Parkinson’s disease

    S. Qian, Y. Sheng, Z. Zhong (Nanjing, China)

    Objective: To examine plasma iron metabolism related indicators in patients with Parkinson’s disease (PD) and investigate the mechanism underlying the tremor-dominant phenotype of PD. Background:…
  • 2018 International Congress

    Longitudinal development of nigral iron load in Parkinson’s Disease

    S. Franthal, L. Pirpamer, C. Rodler, N. Homayoon, M. Koegl, P. Katschnig-Winter, K. Wenzel, C. Langkammer, S. Ropele, R. Schmidt, P. Schwingenschuh (Graz, Austria)

    Objective: We for the first time investigated longitudinal changes of nigral iron load in Parkinson’s disease (PD) measured by Quantitative Susceptibility Mapping (QSM), a highly…
  • 2017 International Congress

    Alpha-synucleinopathy and mitochondrial dysfunction in a cell based model of neurodegeneration: Implications in the pathogenesis of sporadic Parkinson’s disease

    U. Ganguly, O. Sen, A. Ganguly, S. Chakrabarti (Kolkata, India)

    Objective: To elucidate the role of α-synuclein, parkin and mitochondria in a cell-based model of neurodegeneration relevant to Parkinson's disease pathogenesis.  Background: The suggested mechanisms…
  • 2017 International Congress

    Alpha-synuclein protein homeostasis and oligomerization in iron-overloaded cells expressing mutant HFE

    Y. Kim, J. Connor, M. Stahl (Hershey, PA, USA)

    Objective: Study the direct and indirect effects of iron overload on alpha synuclein homeostasis in a genetic model of hemochromatosis (HFE) Background: Parkinson’s disease (PD)…
  • 2017 International Congress

    Dystonia due to bilateral caudate hemorrhage associated with a COL4A1 mutation

    T. Hatano, K. Daida, Y. Hoshino, Y. Li, H. Saitsu, N.c. Matsumoto, N. Hatter (Tokyo, Japan)

    Objective: Pathogenic mutations of COL4A1 are associated with young-onset stroke and porencephaly. We present a case of a 32-year-old female patient with juvenile onset right hand…
  • 2017 International Congress

    Elemental fingerprint as a cerebrospinal fluid biomarker for the diagnosis of Parkinson’s disease

    P. Lingor, A. Leha, B. Michalke, M. Börger, M. Bähr, I. Zerr, F. Maass (Göttingen, Germany)

    Objective: To employ a combination of elemental concentrations in the cerebrospinal fluid (CSF) to identify a diagnostic biomarker profile differentiating patients with idiopathic Parkinson´s disease…
  • 2017 International Congress

    High-Pass Filtered Phase MR Imaging to Detect Longitudinal Motor Associations of Iron Accumulation in Parkinson’s Disease

    A. Martin-Bastida, N. Lao-Kaim, Y. Xing, C. Loane, A. Roussakis, S. Schwarz, N. Valle-Guzman, P. Mahlknecht, X. Li, G. Paul-Visse, H. Widner, M. Politis, T. Foltynie, R. Barker, D. Auer, P. Piccini (London, United Kingdom)

    Objective: To assess whether longitudinal changes in deep grey matter nuclei iron content are associated with declining motor function in Parkinson’s disease over a period…
  • 2017 International Congress

    The Roles of Diet, Exercise, & Supplements in Parkinson’s Disease Progression

    L. Mischley, R. Lau (Kenmore, WA, USA)

    Objective: The goal of this ongoing study is to describe whether modifiable aspects of lifestyle are associated with PD symptom severity and progression. Background: Epidemiological…
  • 2017 International Congress

    Serum soluble transferrin receptor levels correlate with the Hoehn & Yahr stage of Parkinson disease progression

    P. Costa-Mallen, S.-C. Hu, P. Agarwal (Kenmore, WA, USA)

    Objective: To test whether levels of soluble transferrin receptor (sTfR) in the serum of Parkinson disease (PD) patients are correlated with the progression of the disease…
  • 2016 International Congress

    Bristle hair may point to hereditary spastic paraplegia type SPG35/ FAHN

    T.W. Rattay, A.S. Söhn, K.N. Karle, S. Wiethoff, J. Reichbauer, M. Döbler-Neumann, I. Krägeloh-Mann, A. Münchau, B. Wilken, P. Bauer, L. Schöls, R. Schüle (Tübingen, Germany)

    Objective: Finding new phenotypic features or biomarkers in hereditary spastic paraplegia type SPG35 / Fatty Acid Hydroxylase-associated Neurodegeneration (FAHN) to help clinicians to identify this…
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