MDS Abstracts

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

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  • 2016 International Congress

    Do-not-resuscitate utilization in inpatient Parkinson’s disease in the United States

    A. Mahajan, A. Patel, G. Nadkarni, C. Sidiropoulos (Detroit, MI, USA)

    Objective: To investigate Do-not-resuscitate (DNR) order utilization in Parkinson's disease (PD) hospitalizations patients in the United States. Background: DNR order utilization in PD has been…
  • 2016 International Congress

    Assessment of malnutrition in patients with Parkinson’s disease

    O. Yilmaz Kusbeci, I. Inci, B. Donmez Colakoglu, N. Erdogmus Ince, R. Cakmur (Izmir, Turkey)

    Objective: We aimed to assess malnutrition and those at risk of malnutrition in PD patients with an age matched control group using the mini nutritional…
  • 2016 International Congress

    The effect of a structured medication review on quality of life in patients with Parkinson’s disease. An interim analysis

    A. Verbeek, N. Oonk, E. Munster, K. Movig, K. ter Huurne, H. Nijmeijer, J. van der Palen, L. Dorresteijn (Eerbeek, Netherlands)

    Objective: To investigate whether a structured medication review executed by a community pharmacist improves medication adherence and influences quality of life in patients with Parkinson's…
  • 2016 International Congress

    Wrist reveals the fall risk in activities of daily living

    T. Pozaic, R. Foell, A.K. Grebe, W. Stork (Waiblingen, Germany)

    Objective: The focus of our cross-sectional study is on investigation of complex measures in terms of the fall risk (FR). The assessment was performed with…
  • 2016 International Congress

    A 12-month, 2-arm, 2-period, randomized, controlled trial of a digital solution for the management of Parkinson’s disease (PD): Rationale and study design

    S. Papapetropoulos, G. Mitsi (Boston, MA, USA)

    Objective: To collect evidence to support the use of a digital solution to improve health outcomes in PD through remote, timely and appropriate drug adjustments,…
  • 2016 International Congress

    Novel THAP1 missense mutation leading to focal and segmental dystonia

    D. Crosiers, C. Van Broeckhoven, P. Cras (Edegem, Belgium)

    Objective: We have identified a novel heterozygous missense mutation in THAP1 (DYT6 locus) in a patient suffering from craniocervical and upper limb dystonia. We describe…
  • 2016 International Congress

    Familial SPG17/distal hereditary motor neuropathy type V– Complicated hereditary spastic paraplegia with many faces

    T. Musacchio, A.K. Zaum, N. Üceyler, C. Sommer, N. Pfeifroth, K. Reiners, E. Kunstmann, J. Volkmann, S. Rost, S. Klebe (Würzburg, Germany)

    Objective: We present the clinical and genetic results of a SPG17 family with a vast intrafamilial phenotype from subclinical signs to a severe and rapidly…
  • 2016 International Congress

    Reduced thalamo-cortical functional connectivity in asymptomatic LRRK2 mutation carriers

    D. Vilas, B. Segura, C. Pont-Sunyer, M.J. Martí, Y. Compta, F. Valldeoriola, H. Baggio, M. Quintana, A. Bayés, J. Hernández-Vara, M. Calopa, M. Aguilar, C. Junqué, E. Tolosa (Barcelona, Spain)

    Objective: To characterize MRI functional patterns during resting state in asymptomatic LRRK2 mutation carriers. Background: Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are…
  • 2016 International Congress

    Investigation into the genetic etiology in South African Parkinson’s disease patients

    G. Borrageiro, L. Van den Heuvel, S.M.J. Hemmings, S. Seedat, S. Bardien (Cape Town, South Africa)

    Objective: To investigate the genetic etiology in a group of South Africa Parkinson's disease (PD) patients. Background: The genetic etiology of PD is complex and…
  • 2016 International Congress

    Genetic analysis of CHCHD2 gene in Parkinson’s disease in a Taiwanese population

    T.S. Fan, H.I. Lin, C.H. Lin, R.M. Wu (Taipei, Taiwan)

    Objective: To evaluate the genetic mutations of CHCHD2 gene in Taiwanese Parkinson's disease patients. Background: A recent study identified a missense mutation in coiled-coil-helix-coiled-coil-helix domain–containing…
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