MDS Abstracts

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

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  • 2023 International Congress

    Clinical implication of small vessel disease burden on deep brain stimulation outcome in Parkinson’s disease

    J. Lee, S. Jo, S. Lee, MS. Kim, SJ. Chung (Seoul, Republic of Korea)

    Objective: We aimed to investigate the correlation between the small vessel disease (SVD) burden and the 1-year outcome after the globus pallidus interna (GPi) deep…
  • 2023 International Congress

    Gender-Specific Classification Models for Parkinson’s Disease using Non-Motor Symptoms and DNA Methylation Data

    MZA. Ali, PSD. Dholaniya (Hyderabad, India)

    Objective: In Parkinson's disease (PD) non-motor symptoms often appear before the motor symptoms. Detecting and understanding these non-motor symptoms and their possible genetic or epigenetic…
  • 2023 International Congress

    Monoamine loss and depression in Parkinson’s disease: a PET study

    BL. Xu, XL. Liu, SY. Liu, O. Barret, G. Tamagnan, H. Qiao, TB. Song, J. Lu, P. Chan (Beijing, China)

    Objective: 1)To evaluate the imaging manifestations of monoamine changes in PD patients with depression through 18F-FP-DTBZ PET; 2) To explore the relationship between monoamine changes…
  • 2023 International Congress

    Validation of the EQ-5D-3L in Spinocerebellar Ataxia (SCA)

    M. Buchholz, N. Weber, A. Rädke, J. Faber, T. Schmitz-Hübsch, H. Jacobi, F. Xie, T. Klockgether, B. Michalowsky (Greifswald, Germany)

    Objective: Our study aims to assess the acceptability, validity and responsiveness of the EQ-5D-3L in SCA types 1, 2, 3 and 6. Background: Although health-related…
  • 2023 International Congress

    Structural MRI and tremor analysis in the differential diagnosis of rest tremor

    F. Aracri, M. Bianco, C. Calomino, M. de Maria, B. Vescio, J. Buonocore, A. Sarica, A. Quattrone (Catanzaro, Italy)

    Objective: This study aimed to differentiate between essential tremor with rest tremor (rET) and tremor-dominant Parkinson’s disease (td-PD) patients through a machine learning (ML) approach…
  • 2023 International Congress

    Early functional disruption in body-first compared to brain-first Parkinson’s disease

    M. Conti, R. Bovenzi, R. Cerroni, T. Schirinzi, M. Pierantozzi, N. Mercuri, A. Stefani (Rome, Italy)

    Objective: To analyze differences in functional connectivity (FC) between Parkinson’s disease (PD) patients with and without premotor REM behavior disorder (pRBD), by means of high-density…
  • 2023 International Congress

    Risk factors for Freezing of Gait in Parkinson’s Disease: A Systematic Review and Meta-analysis

    X. Zheng, J. Liu, S. Wang, R. Ou, C. Li, H. Shang (Chengdu, China)

    Objective: To comprehensively identify risk factors of freezing of gait (FOG) in Parkinson’s disease (PD), we performed a meta-analysis by combining the results of previous…
  • 2023 International Congress

    Role of ATP10B variants in Parkinson Disease in a southern Spanish cohort

    R. Díaz-Belloso, MT. Periñan, M. Martín-Bornez, S. García-Díaz, M. Bonilla-Toribio, D. Buiza-Rueda, R. Pineda-Sánchez, L. Muñoz-Delgado, S. Jesús, D. Macías-García, A. Adarmes-Gómez, F. Carrillo, P. Mir, P. Gómez-Garre (Sevilla, Spain)

    Objective: The objective of our study was to evaluate the role of ATP10B variants in Parkinson disease (PD) in a southern Spanish cohort of PD…
  • 2023 International Congress

    Late-onset cerebellar ataxia revealing a Pantothenate-kinase-associated neurodegeneration

    S. Laroussi, S. Sakka, S. Daoud, N. Bouattour, K. Moalla, N. Farhat, M. Damak, C. Mhiri (Sfax, Tunisia)

    Objective: Recall a case of genetic late-onset cerebellar ataxia with a specific clinical and radiological feature highly suggestive of Pantothenate-kinase-associated neurodegeneration(PKAN). Background: Cerebellar ataxia is…
  • 2023 International Congress

    Impaired Nt-acetylation and the Golgi, a new disease mechanism leading to autosomal recessive primary familial brain calcifications

    V. Chelban, H. Aksnes, L. Lamonica, R. Maroofian, L. Seabra, P. Devic, J. Vandrovcova, D. Murphy, A. Pagnamenta, N. Wood, R. Horvath, A. Ernst, J. Rothman, M. Mcentagart, Y. Crow, G. Nicolas, T. Arnesen, H. Houlden (London, United Kingdom)

    Objective: To identify new disease-gene in unsolved autosomal recessive primary familial brain calcifications. Background: Primary familial brain calcification (PFBC) is characterized by calcium deposition in the brain,…
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