MDS Abstracts

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

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  • 2023 International Congress

    Aberrant brain plasticity in patients with Parkinson’s disease and levodopa-induced dyskinesias

    P. Sanginario, B. Angeloni, C. Piano, AR. Bentivoglio, R. Di Iorio, F. Bove, P. Calabresi (Rome, Italy)

    Objective: We performed this monocentric cross-sectional study aimed to identify the alterations of cortical plasticity at primary motor cortex (M1) in PD patients with and…
  • 2023 International Congress

    Hospital based motor cognitive rehabilitation training. what after? An intervention aimed at patients support between admissions

    C. Siri, A. Carollo, G. Manoni, M. Canesi (Milano, Italy)

    Objective: The present intervention aimed at evaluating the adherence to the suggested training after dismission from the motor cognitive rehabilitation unit and to help patients…
  • 2023 International Congress

    At-home adaptive deep brain stimulation improves motor fluctuations and quality of life in patients with Parkinson’s disease: a single-blind randomized study

    C. Oehrn, S. Cernera, L. Hammer, M. Shcherbakova, J. Yao, A. Hahn, C. Smyth, S. Little, P. Starr (San Francisco, USA)

    Objective: We evaluated the effect of at-home adaptive deep brain stimulation (aDBS) based on personalized neural biomarkers on motor symptoms and quality of life (QoL)…
  • 2023 International Congress

    Botulinum toxin treatment for focal dystonia in a Tunisian cohort

    M. Jamoussi, H. Benrhouma, M. Ben Hafsa, T. Ben Younes, Z. Miladi, H. Klaa, I. Kraoua, N. Gouider Khouja, I. Ben Youssef (Tunis, Tunisia)

    Objective: Our aim was to report the etiology, management and outcome of patients with focal dystonia. Background: Focal dystonia (FD) is characterized by involuntary muscle…
  • 2023 International Congress

    VPS11 associated movement disorder in a pediatric case

    E. Serdaroglu, A. Serdaroglu (Ankara, Turkey)

    Objective: Disorders of intracellular trafficking may present with different neurological features such as pediatric movement disorders. Background: A 15-year-old boy presented with a three-year history…
  • 2023 International Congress

    The Quebec Parkinson Network (QPN): Interdisciplinary Collaboration in Parkinson’s Disease and Related Disorders Research.

    M. Blais, S. Bogard, C. Degroot, N. Dupré, E. Fon (Quebec City, Canada)

    Objective: By creating a participant registry, gathering information on participants, and ensuring appropriate data exchange with research groups, the QPN's primary goal is to increase…
  • 2023 International Congress

    Gluten-free diet in Parkinson’s disease patients – feasibility, safety and preliminary results

    H. Brozova, K. Polakova, M. Fialova, T. Gentileova, J. Rusz, D. Funda (Prague, Czech Republic)

    Objective: The primary objective of this project is to evaluate the effect of long administered gluten-free diet (GFD) on motor symptoms of Parkinson's disease (PD).…
  • 2023 International Congress

    Chorea as a clinical manifestation in adult-onset of metachromatic leukodystrophy

    NT. Dragašević Mišković, A. Milovanović, M. Branković, I. Novaković, I. Petrović, A. Tomić Pešić, M. Svetel, VS. Kostić (Belgrade, Serbia)

    Objective: Here we want to present a patient with chorea as part of clinical manifestation of adult onset of metachromatic leukodystrophy. Background: Metachromatic leukodystrophy is…
  • 2023 International Congress

    Correlation between rem sleep disorders and neurocognitive defects in patients with parkinson´s disease

    M. Castillo, A. Mariñez, J. Duran, I. Joga, A. Morales (santo domingo, Dominican Republic)

    Objective: The objective of the following study was to verify the correlation between cognitive disordersand REM sleep disorders. Background: REM sleep disorder affect a large…
  • 2023 International Congress

    Heterozygous aprataxin gene mutation associated with atypical multiple system atrophy phenotype: a case report

    A. Imarisio, A. Pilotto, A. Lupini, G. Biasiotto, I. Zanella, I. Palmieri, EM. Valente, A. Padovani (Pavia, Italy)

    Objective: We describe a 73-year old patient carrying a heterozygous mutation in aprataxin (APTX) gene presenting multiple system atrophy-parkinsonian variant (MSA-P). Background: Ataxia with oculomotor…
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