MDS Abstracts

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

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  • 2024 International Congress

    Prospective Study of Gait and Multimodal MRI Biomarkers for Multiple System Atrophy

    F. Marchand, R. Viard, D. Devos, L. Defebvre, T. Ollivier, D. Guehl, G. Kuchcinski, C. Moreau (LILLE, France)

    Objective: We aimed to develop new multimodal biomarkers allowing objective monitoring of early MSA progression to improve outcome definition for future neuroprotective trials. Background: MSA…
  • 2024 International Congress

    Characteristics of Language Abnormalities in Multiple System Atrophy and Parkinson’s Disease

    M. Subert, M. Novotny, P. Dusek, J. Klempir, J. Rusz, T. Tykalova (Prague, Czech Republic)

    Objective: We characterized complex language profile and explore diagnostic potential of automated language analysis of natural spontaneous speech in differentiation between multiple system atrophy (MSA)…
  • 2024 International Congress

    Longitudinal progress and clinical relevance of 18F-Florzolutau PET in patients with PSP: a one-year follow-up study

    J. Wang, F. Liu, C. Zuo (Shanghai, China)

    Objective: Here we aimed to explore the progress of 18F-Florzolotau PET and its clinical relevance in patients with PSP during one-year follow-up. Background: The 18F-Florzolotau…
  • 2024 International Congress

    Spectrum of Sleep abnormalities in Patients with Progressive supranuclear palsy

    M. Nanjunda Swamy, S. Dey, N. Kamble, V. Holla, R. Mahale, P. Pal, M. Debnath, R. Yadav (Bengaluru, India)

    Objective: We studied the clinical characteristics of patients with Progressive Supranuclear Palsy (PSP) with particular reference to sleep disorders and their associated features. Background: PSP…
  • 2024 International Congress

    Pisa Syndrome as an early presenting feature of Corticobasal Ganglionic degeneration [CBGD]

    M. Matta, N. Sawal, A. Prasad (Chandigarh, India)

    Objective: To describe Pisa syndrome as an early presenting feature of CBGD and add to literature on CBGD so that neurologists can suspect CBGD when…
  • 2024 International Congress

    Free-water MRI Correlates of Pareidolia in Dementia with Lewy Bodies

    S. Chiu, R. Chen, W. Wang, G. Smith, B. Boeve, R. Savica, V. Ramanan, J. Fields, N. Graff-Radford, T. Ferman, K. Kantarci, J. Leverenz, N. Armstrong, D. Vaillancourt (Scottsdale, USA)

    Objective: To evaluate free-water (FW) differences in patients with dementia with Lewy bodies (DLB) with versus without pareidolias Background: Pareidolias are a type of illusion…
  • 2024 International Congress

    CSF Neurogranin Levels Are Decreased in Parkinson Disease

    H. Hwang, R. Miller, T. Cash, A. Eid, E. Herries, R. White Iii, B. Maiti, S. Schindler, J. Jackson, J. Perlmutter, M. Campbell, P. Kotzbauer (SAINT LOUIS, USA)

    Objective: To investigate CSF neurogranin differences in participants with Parkinson disease (PD) and controls and to examine its association with motor and cognitive symptoms. Background:…
  • 2024 International Congress

    Prediction of Time-to-Phenoconversion to Parkinsonism in Idiopathic REM Sleep Behavior Disorder (iRBD)

    SM. Fereshtehnejad, A. Delva, Y. Zeighami, M. Dadar, A. Pelletier, J. Montplaisir, JF. Gagnon, C. Marras, R. Postuma (Toronto, Canada)

    Objective: To develop a tool for the prediction of time-to-phenoconversion in individuals with iRBD during the prodromal stage of parkinsonism. Background: Parkinson’s disease(PD) and dementia…
  • 2024 International Congress

    Perry Syndrome due to a DCTN1 novel variant

    P. Lorenzo-Barreto, I. Muro-García, E. Casas-Peña, JP. Romero-Muñoz, L. López-Manzanares (Madrid, Spain)

    Objective: To report the clinical features of a patient with Perry syndrome (PS) due to a heterozygous novel pathogenic variant in the DCTN1 gene. Background:…
  • 2024 International Congress

    Non motor symptoms assessment in Primary Familial Brain Calcification, survey on a cohort

    G. Bonato, M. Carecchio (Padova, Italy)

    Objective: Defining the burden of non-motor symptoms in Primary Familial Brain Calcification Background: PFBC is a rare neurodegenerative disorder of adulthood characterized by calcium deposition…
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