MDS Abstracts

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

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  • 2023 International Congress

    Patterned alternating-coloured strips for freezing of gait – Novel solution for a disabling symptom.

    M. Matta, N. Sawal, D. Bansal (Chandigarh, India)

    Objective: To evaluate a novel method of visual cueing using patterned alternating-coloured strips made of electrical tape for freezing of gait. Background: Freezing of gait…
  • 2023 International Congress

    Assessing akinesia domains during multitasking in Parkinson’s disease

    V. Dzialas, M. Banwinkler, M. Höhnig, T. van Eimeren (Cologne, Germany)

    Objective: To explore performance differences in single- versus dual-tasking conditions between healthy controls (HC) and Parkinson's disease (PD) patients. Background: Akinesia, comprising slowness (bradykinesia), reduction…
  • 2023 International Congress

    Oculomotor changes in the premotor stage of LRRK2- G2019S associated Parkinson’s disease.

    M. Rivera Sánchez, C. Lage Martínez, A. Sánchez Rodríguez, M. Sierra Peña, I. González Aramburu, L. Manrique Arregui, MV. Sánchez Peláez, C. García Cena, A. Calvo Córdoba, J. Madera Fernández, J. Martín Arroyo, J. Infante Ceberio (Santander, Spain)

    Objective: To analyse oculomotor differences among idiopathic PD patients (iPD), LRRK2-G2019S PD patients (LRRK2-G2019S PD), asymptomatic carriers of LRRK2-G2019S mutation (AsG2019S), and controls, evaluated by…
  • 2023 International Congress

    New wearable technology for quantification of freezing of gait in school going adolescent with pediatric movement disorders

    V. Sharma, M. Gautam (Agra, India)

    Objective: To study quantification of  freezing of gait  (FOG) and falls of patients data in school going adolescent with pediatric movement disorders by wearable device…
  • 2023 International Congress

    First case of sporadic ATP6AP2 Mutation reported in Asia in a Parkinson’s Disease patient

    K. Shukla, N. Sawal (Chandigarh, India)

    Objective: Genetic analysis of Parkinson's Disease (PD) with features of spasticity by Whole Exome Sequencing (WES) and use of its result for treatment modification to…
  • 2023 International Congress

    Deep Brain Stimulation in Parkinson’s Disease Patients: A One Year Follow-up in the Understudied Geography of Brazil

    M. Faria, A. Novicki, F. Godinho, Y. Souza, J. Woods, K. Stromberg, R. Paolillo, C. Rocha (Belo Horizonte, Brazil)

    Objective: This study aimed to evaluate the role of deep brain stimulation (DBS) in the improvement of health-related quality of life (HR QoL) outcomes in…
  • 2023 International Congress

    Evaluation of a novel Phosphodiesterase 5 inhibitor as a potential therapeutic agent in P301S transgenic mouse model of tauopathy.

    S. Elfarrash, S. Eldusoky, M. Abdel-Halim, M. Salama, S. El-Khodery, M. Youssef (Mansoura, Egypt)

    Objective: In the current study, we evaluated a newly developed compound with a 1,3,5-trisubstituted pyrazoline scaffold with an improved PDE5 inhibitory potency as a potential…
  • 2023 International Congress

    Concordant RNA patterns in Parkinson’s disease brain and peripheral blood.

    K. Irmady, C. Hale, J. Fak, R. Qadri, T. Carroll, S. Przedborski, R. Darnell, S. Simelane (NEW YORK, USA)

    Objective: To investigate the molecular correlates of clinical heterogeneity in Parkinson’s disease (PD) in the striatum and peripheral blood. Background: The molecular basis for clinical…
  • 2023 International Congress

    Neuroimaging and correlation with functional status in children with cerebral palsy

    M. Ben Hafsa, H. Benrhouma, M. Jamoussi, T. Ben Younes, Z. Miladi, A. Zioudi, H. Klaa, I. Kraoua, S. Nagi, I. Ben Youssef-Turki (Tunis, Tunisia)

    Objective: To analyse the neuroimaging findings and to establish a correlation between clinical features and magnetic resonance imaging (MRI) patterns in children with cerebral palsy…
  • 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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