MDS Abstracts

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

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  • 2024 International Congress

    Role of Telemedicine- Versus Outpatient-Based Initiation And Management of Atkins Diet Therapy In Postmenopausal Women With Drug-Resistant Parkinson’s Disease During The COVID-19 Pandemic

    M. Sharma, S. Sinha (Pimpri, India)

    Objective: To explore the satisfaction, effectiveness, and safety of online modified Atkins diet (MAD) initiation and follow-up by comparing a group of work-from-home postmenopausal women…
  • 2024 International Congress

    Characterization of Muscle activity before and during Freezing of Gait Episodes

    E. Jafari, S. Pardoel, A. Alakhras, J. Kofman, E. Lemaire, J. Nantel (Ottawa, Canada)

    Objective: Objective: The study aims to characterize surface electromyography (EMG) activity in the distal and proximal leg muscles of 17 participants with Parkinson’s disease (PD)…
  • 2024 International Congress

    iPSC-Based Modeling of SCA12 for Targeted Therapeutic Screening

    B. Reddy, A. Gerutshang, R. Roy, R. Banerjee, S. Chowdhury, H. Kumar, S. Chattarji (Kolkata, India)

    Objective: 1. To identify a cohort of genetically confirmed SCA12 patients of Indian origin, derive iPSCs, progenitor cells and neurons from peripheral blood samples2. To…
  • 2024 International Congress

    A Head-Turning Case of SCA10 with Dystonia

    S. Marmol, V. Armengol, D. Shpiner (Miami, USA)

    Objective: Present a SCA10 patient presenting with rare phenomenology of dystonia in addition to ataxia. Background: The spinocerebellar ataxias (SCAs) are a heterogenous group of…
  • 2024 International Congress

    Ataxia, tremor, fasciculations and hemiparesis in a GBA1 heterozygous female carrier

    I. Sarac, H. Sarac, F. Borovečki, N. Henigsberg, I. Jurak, K. Zic (Zagreb, Croatia)

    Objective: Our aim is to present a woman carrying a heterozygous GBA1 mutation who developed exclusively neurological symptoms in adulthood. Background: The diagnosis of Gaucher…
  • 2024 International Congress

    paraneoplastic cerebellar ataxia: a rare cause of late-onset ataxia

    H. Boussaid, R. Zouari, D. Ben Mohamed, A. Rachdi, Z. Said, F. Nebli, S. Ben Sassi (monastir, Tunisia)

    Objective: investigate the clinical features, imaging findings and immunological characteristics of Paraneoplastic cerebellar ataxia (PCA) in our cohort. Background: Paraneoplastic cerebellar ataxia (PCA) is a…
  • 2024 International Congress

    Syndrome of Progressive Ataxia with Palatal Tremors (PAPT) with Hypertrophied Bilateral Inferior Olives in a young Indian Female

    P. Saroja Bylappa, D. Garg, A. Agarwal, A. Garg, A. Srivastava (New Delhi, India)

    Objective: To report and extend the clinical and radiological features of Progressive Ataxia and Palatal Tremors (PAPT) syndrome. Background: Hypertrophic degeneration of olivary nucleus is…
  • 2024 International Congress

    Bilateral Fronto-Temporal Lobar Atrophy: An Atypical Magnetic Resonance Imaging Finding in Neuroacanthocytosis

    N. Ranjan, AM. Kumar, AB. Ranjan (Patna, India)

    Objective: In Neuroacanthicytosis,to the best of our knowledge, bilateral fronto-temopral lobar atrophy associated with neuroacanthocytosis has not been reported. We report herein a case of…
  • 2024 International Congress

    Deep Brain Stimulation in Dystonia: Investigating Differential Response by Dystonia Distribution

    S. Yarlagadda, M. Patel, S. Rajagopalan, H. Jinnah, S. Factor, S. Miocinovic, L. Scorr (Decatur, USA)

    Objective: To quantify the response of isolated non-acquired dystonia to deep brain stimulation (DBS) of the globus pallidus interna (GPi) across multiple body regions. Background:…
  • 2024 International Congress

    Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia

    T. Wirth, E. Roze, C. Delvallée, O. Trouillard, N. Drouot, P. Damier, C. Boulay, M. Bourgninaud, P. Jegatheesan, A. Sangare, S. Forlani, B. Gaymard, R. Hervochon, V. Navarro, N. Calmels, A. Schalk, C. Tranchant, A. Piton, A. Méneret, M. Anheim (Strasbourg, France)

    Objective: The aim is to identify the missing genetic causes of Paroxysmal Kinesigenic Dyskinesia (PKD) Background: Although the group of genes associated with PKD is…
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