2026 International Congress

October 4-8, 2026. Seoul, Korea.

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Identification of a Novel MYORG Mutation in Autosomal Recessive Idiopathic Basal Ganglia Calcification-7 (IBGC7): A Case Report

W. Kamel, D. Al Mehatab, L. Bastaki (Beni-Suef, Egypt)
Identification of a sporadic dystonia-related brain network using resting-state fMRI and machine learning

O. Omilabu, D. Truong, K. Nguyen, S. Vacca, T. Fitzpatrick, A. Oh, M. Neithammer, N. Nguyen, D. Eidelberg, A. Vo (Great Neck, USA)
Identification of Alpha-synuclein Pathology in Dementia with Lewy Body Participants by Seed Amplification Assay

C. Farris, S. Weber, Y. Ma, M. Starke, B. Mollenhauer, L. Concha (San Diego, USA)
Identification of Alpha-synuclein Pathology in Idiopathic Rapid Eye Movement Sleep Disorder Participants by Seed Amplification Assay

C. Farris, S. Weber, Y. Ma, M. Starke, B. Mollenhauer, L. Concha (San Diego, USA)
Identification of Alpha-synuclein Pathology in Primary Tauopathies by Seed Amplification Assay

C. Farris, S. Weber, Y. Ma, M. Starke, D. Irwin, A. Siderowf, B. Mollenhauer, L. Concha (San Diego, USA)
Identification of Candidate Cerebrospinal Fluid Biomarkers in Multiple System Atrophy Using Mass Spectrometry‑Based Proteomics in CSF Biobank Samples

P. Kallunki, M. Lubas, J. Fussing Tengberg, V. Carmelo, S. Virreira Winter, P. Geyer (Valby, Denmark)
Identification of DAGLB Variants in Chinese Patients With Early-Onset Parkinson’s Disease

W. Ren, J. Huang, Y. Guan, W. Zhao, Y. Guo, R. Hua, H. Liu (Changsha, China)
Identification of Digital Measures of Motor Progression from In-Clinic Assessments in Early Parkinson’s Disease for Composite Digital Biomarkers: Results from WATCH-PD

J. Ren, S. Zhai, J. Shen, O. Patil, R. Baumgartner, ER. Dorsey, J. Adams, D. Mehrotra, M. Dockendorf (Rahway, USA)
Identification of Discriminative Odorants for Parkinson’s Disease and Their Clinical Correlates: A Population-Specific Short-Form Approach

YH. Lin, TC. Fang, MH. Chang, YJ. Guo (Taichung, Taiwan)
Identification of Novel FA2H Mutations in Patients with Hereditary Spastic Paraplegia Type 35 (SPG35)

L. Wang, X. Jin, W. Luo (Hangzhou, China)

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