MDS Abstracts

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

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  • 2024 International Congress

    Effect of Ecopipam, a Selective Dopamine-1 Receptor Antagonist, on Tic Characteristics as Assessed by the YGTSS: Results from a Phase IIb Randomized, Double-blind, Placebo-controlled Clinical Trial in Tourette Syndrome

    D. Gilbert, G. Karkanias, S. Atkinson, F. Munschauer, S. Wanaski, T. Cunniff (Cincinnati, USA)

    Objective: Assess the effect of ecopipam treatment on motor and phonic/vocal tic characteristics: number, frequency, intensity, complexity, and interference comprising the Yale Global Tic Severity…
  • 2024 International Congress

    Reliability of neurophysiological and cerebral tremor features in Parkinson’s disease

    L. Angelini, KRE. Berg, MF. Dirkx, M. Bologna, BR. Bloem, RCG. Helmich (Pozzilli

    Objective: We aim to assess the stability and intra-individual reliability of clinical, neurophysiological and neuroimaging Parkinson’s Disease (PD) tremor parameters. Background: The cerebello-thalamo-cortical circuit (CTC)…
  • 2024 International Congress

    Prevalence of Phosphorylated Alpha-Synuclein in Skin Biopsies of Essential Tremor Patients

    S. Bellows, N. Vanegas Arroyave, J. Jankovic (Housont, USA)

    Objective: To examine the prevalence of phosphorylated alpha-synuclein in nerve fibers in patients with essential tremor (ET) and ET plus. Background: Although Essential Tremor (ET)…
  • 2024 International Congress

    The Intention Component of Postural Tremor in Essential Tremor

    K. Valestrino, P. Kassavetis (Salt Lake City, USA)

    Objective: This study seeks to better characterize postural tremor in ET and to investigate the effect of intention and visual input on the amplitude and…
  • 2024 International Congress

    A novel G413S mutation in the CSF1R gene causes Hereditary Diffuse Leucoencephalopathy with axonal Spheroids; clinically overlapping features of Parkinsonism

    ANW. Ullah, MZB. Badshah (Peshawar, Nepal)

    Objective: The current study was designed to investigate the genetic cause of atypical Parkinsonism is a multigenerational Pakistani family Background: Hereditary Diffuse Leucoencephalopathy with axonal…
  • 2024 International Congress

    OPTN gene associated with corticobasal syndrome: a novel multi-exon deletion and literature review

    G. Bonato, M. Ginevrino, B. Savini, D. Ciprietti, P. Santurelli, E. Gasparoli, C. Gabelli, G. Sorarù, R. Biundo, M. Carecchio, A. Guerra, L. Salviati, A. Antonini (Padova, Italy)

    Objective: To describe a novel case of OPTN multiexon deletion causing a peculiar CBS-ALS phenotype. Background: While traditionally classified as distinct clinical entities, corticobasal syndrome…
  • 2024 International Congress

    Association of polygenic risk score of the LRRK2 gene for Parkinson’s disease with lysosomal hydrolase activities in the Russian Population based on genetic profile and established risk factors

    T. Usenko, K. Basharova, A. Bezrukova, K. Senkevich, I. Miliukhina, A. Timofeeva, E. Zakharova, S. Pchelina (Gatchina, Russian Federation)

    Objective: To studied a previously proposed polygenic risk scores (PRSs) for PD selected for the LRRK2 gene in a genetic data set of Russian population…
  • 2024 International Congress

    Genetic Study of polymorphism of cytokines in Parkinson’s disease.

    S. Frikha, O. Ben Othmen, S. Fezai, A. Achouri, M. Ben Mahmoud, S. Fray, H. Jamoussi, M. Fredj, N. Ben Ali (Tunis, Tunisia)

    Objective: The aim of our study was to conduct a cohort that demonstrates genetic variations in cytokines genes involved in the physiopathology, the development and…
  • 2024 International Congress

    Comorbidities in genetic Parkinson’s Disease: comparison between LRRK2, GBA1, and non-mutated PD

    G. Di Rauso, F. Pirone, G. Franco, F. Arienti, I. Trezzi, E. Frattini, F. Cavallieri, V. Rispoli, F. Valzania, E. Monfrini, A. Di Fonzo (Reggio Emilia, Italy)

    Objective: To examine the occurrence of medical comorbidities associated with genetic form of Parkinson’s disease (GBA1-PD and LRRK2-PD) compared to a cohort of non-mutated PD…
  • 2024 International Congress

    Expanding the PD GENEration Study to increase clinical genetic testing and counseling using whole genome sequencing among diverse Parkinson’s disease (PD) populations

    K. Ghosh Galvelis, A. Naito, M. Dini, S. Rao, R. Deleon, A. Coral-Zambrano, T. Foroud, P. Hodges, L. Heathers, J. Verbrugge, L. Cook, J. Schulze, M. Totten, A. Hall, K. Marder, I. Mata, N. Mencacci, T. Simuni, M. Nance, M. Schwarzschild, A. Wills, S. Lawrence, P. Ponger, J. Beck, R. Alcalay (New York, USA)

    Objective: To provide Clinical Laboratory Improvement Amendments (CLIA) genetic testing using whole genome sequencing and disclosure of 7 PD relevant genes and secondary health-related genetic…
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