MDS Abstracts

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

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  • 2018 International Congress

    Identification of gut microbial genes in Parkinson’s disease by shotgun metagenomic analysis

    Y. Qian, X. Yang, S. Xu, S. Chen, Q. Xiao (Shanghai, China)

    Objective: To carry out deep analysis on gut microbiome in patients with Parkinson’s disease (PD) and to evaluate the potential application for diagnosing PD patients…
  • 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…
  • 2018 International Congress

    Ubiquitin carboxyl-terminal hydrolase 1 (UCHL1) -mediated ubiquitination attributed to localization of Mortalin to mitochondria

    L. Wu, W. Yang, Y. Tan, J. Ding, S. Chen (Shanghai, China)

    Objective: The pathogenic mechanism of UCHL1 in PD remains unclear. In this study, we aimed to investigate the role of UCHL1 in the pathogenesis of…
  • 2018 International Congress

    Gaucher’s disease (GD) and Parkinsonism: An analysis from patients to relatives

    I. Trezzi, E. Monfrini, E. Cassinerio, I. Motta, F. Nascimbeni, F. Carubbi, N. Bresolin, G. Comi, M. Cappelllini, A. Di Fonzo (Milan, Italy)

    Objective: To identify parkinsonian features in a cohort of GD patients and their relatives. Background: GD is a lysosomal storage disorder caused by GBA1 mutations…
  • 2018 International Congress

    Early-onset Parkinson’s disease in seven patients with heterozygosity for parkin mutation

    C. Lima, A. Novo, M. Sousa, M. Almeida, A. Morgadinho, C. Januário (Coimbra, Portugal)

    Objective: To present and discuss a series of 7 patients with early-onset Parkinson’s Disease and heterozygosity for PARK2 mutation. Background: Parkin mutation in homozygosity or…
  • 2018 International Congress

    Early-onset parkinsonism and epilepsy: A Tunisian family carrying a novel SYNJ1 mutation

    S. Ben Romdhan, R. Zouari, S. Sakka, N. Farhat, O. Hdiji, H. Haj Kacem, M. Dammak, C. Mhiri (Sfax, Tunisia)

    Objective: We report two siblings from a Tunisian family with juvenile Parkinsonism associated with tonic-clonic seizures and good response to levodopa therapy carrying a novel…
  • 2018 International Congress

    Neuronal KIF5b deletion induces striatum-dependent locomotor impairments and defects in membrane presentation of dopamine D2 receptors

    T. Falzone, L. Cromberg, M. Alloatti, I. Fernandez Bessone, T. Saez (Buenos Aires, Argentina)

    Objective: In this study we aim to elucidate the role of Kif5b motor subunit in the nigrostriatal pathway. We have generated different conditional knockout mice…
  • 2018 International Congress

    SIRT1/AMPK pathway is involved in neuroprotective effects of resveratrol on MPTP-induced neuron loss

    Y.J. Guo, S.Y. Dong, W.J. Zhao, Y.C. Wu (Shanghai, China)

    Objective: The present study was carried out to observe the neuroprotective effects of RV on MPTP-induced mouse model of PD, and explore its potential neuroprotective…
  • 2018 International Congress

    A review of modifiers of Parkinsonism in the Leucine-rich repeat kinase 2 (LRRK2) population

    J. Staisch (Portland, OR, USA)

    Objective: To review and examine the most current identified modifiers of Parkinsonism in the LRRK2 population. Background: LRRK2 is a protein with multiple domains and…
  • 2018 International Congress

    Lack of TMEM230 mutations in patients with familial and sporadic Parkinson’s disease in a Taiwanese population

    T. Fan, C. Lin, H. Lin, M. Chen, R. Wu (Taoyuan, Taiwan)

    Objective: To confirm the role of mutations in transmembrane protein 230 (TMEM230) in a large number of PD patients and controls in a Taiwanese population.…
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