MDS Abstracts

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

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  • 2018 International Congress

    Psychogenic Palatal Tremor: A Case Report

    A. Tüfekçi, Ç. Hocaoğlu, D. Yanoğlu, K.S. Karataş (Rize, Turkey)

    Objective: Palatal tremor(PT) is an extremly rare movement disorder, defined by rhythmic movements of the soft palate. PT is divided into two forms: essential PT(EPT)…
  • 2018 International Congress

    The effect of thalamic and subthalamic deep brain stimulation on speech in patients with essential tremor: A prospective, randomized, double-blind crossover study

    J. Becker, T. Dembek, P. Reker, J. Petry-Schmelzer, D. Mücke, V. Visser-Vandewalle, M. Barbe (Cologne, Germany)

    Objective: To investigate the effect of thalamic (ventral intermediate nucleus, VIM) and subthalamic (posterior subthalamic area, PSA) deep brain stimulation (DBS) in patients with essential…
  • 2018 International Congress

    Somatosensory temporal discrimination in Parkinson’s disease, dystonia and essential tremor: Pathophysiological and clinical implications

    N. Manzo, A. Conte, D. Belvisi, G. Ferrazzano, G. Fabbrini, A. Berardelli (Rome, Italy)

    Objective: To investigate whether changes in the somatosensory temporal discrimination threshold (STDT) in Parkinson’s disease (PD) and dystonia reflect the involvement of specific neural structures…
  • 2018 International Congress

    Neuropsychological Assessment of Cognitive Dysfunction in Parkinson’s Disease: A Comparison of Four Screening Instruments

    S. Schnitzler, L. Flitsch, S. Kaesberg, J. Kessler, E. Kalbe, M. Barbe (Cologne, Germany)

    Objective: To compare four different neuropsychological screening instruments (DemTect, Mattis Dementia Rating Scale (MDRS), Mini Mental State Examination (MMSE) and Parkinson Neuropsychometric Dementia Assessment (PANDA))…
  • 2018 International Congress

    Affective Theory of Mind Impaired in Parkinson’s Disease: Negative- and Neutral- specific impairments of Emotion State Decoding

    C.H. Tan, S.C. Tu, R.L. Yu (Kaohsiung, Taiwan)

    Objective: The primary aim of this study was to investigate whether the ability to interpret positive, negative, or neutral emotion from a pair of photographed…
  • 2018 International Congress

    Hypertriglyceridemia is associated with Parkinson disease mild cognitive impairment (PD-MCI)

    S. Ng, KY. Tay, X. Huang, NSY. Chia, S. Archaryya, F. Setiawan, ZH. Lu, J. Tan, YL. Ng, MC. Wen, A. Ng, W. Au, EK. Tan, L. Tan (Singapore, Singapore)

    Objective: Our study aimed to characterise Parkinson disease (PD) mild cognitive impairment (PD-MCI) in early PD and to identify biomarkers associated with PD-MCI. Background: Approximately…
  • 2018 International Congress

    Dual task walking differentially affects toe clearance in Lewy body disease: A contributor to dynamic falls risk?

    L. Alcock, R. McArdle, L. Aubrook, B. Galna, A. Thomas, L. Rochester (Newcastle upon Tyne, United Kingdom)

    Objective: To evaluate the change in gait and minimum toe clearance when walking under dual task in different dementia sub-types as a contributor to dynamic…
  • 2018 International Congress

    Kufor-Rakeb Syndrome with prominent dystonia and new mutations in ATP13A2 gene in two siblings

    T. Yamasaki, J. Thakkar, L. Noll, J. Slevin (Lexington, KY, USA)

    Objective: To describe new genetic mutations and unusual clinical findings in two siblings with Kufor Rakeb syndrome, an autosomal recessive etiology of parkinsonism. Background: Kufor-Rakeb…
  • 2018 International Congress

    Increased Parkin expression in a PARK20 (SYNJ1 mutation) iPSCs-based model

    W. Mandemakers, R. Masius, E. Berger, M. Grochowska, M. Quadri, M. Minneboo, M. Picillo, P. Barone, J. Schwamborn, V. Bonifati (Rotterdam, Netherlands)

    Objective: To generate mechanistic insight into how the SYNJ1 p.Arg258Gln mutation leads to neurodegeneration in juvenile Parkinsonism. Background: In humans, the SYNJ1 homozygous p.Arg258Gln missense…
  • 2018 International Congress

    LRRK2 and GBA genetic mutations are not uncommon in an unselected Ashkenazi elderly cohort with PD

    S. Isaacson, J. Isaacson (Boca Raton, FL, USA)

    Objective: Analysis of positive LRRK2 and GBA gene mutations, demographic characteristics, and family history in 1200 consecutive Ashkenazi patients with PD who had genetic testing…
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