2026 International Congress

October 4-8, 2026. Seoul, Korea.

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Probable Corticobasal Syndrome Presenting as Writer’s Cramp: A Case Report

B. Dias, K. Alves, T. Goncalves, D. Faria, R. Pinto, S. Silva (Sao Paulo, Brazil)
Probable RBD and Anxiety in Early Parkinson’s Disease Predict Subsequent Functionally Disabling Medication-Refractory Tremor

D. Ledingham, S. Sathyanarayana, R. Iredale, C. Stewart, V. Foster, D. Galley, M. Baker, N. Pavese (Newcastle Upon Tyne, United Kingdom)
Probiotic Y7 Intervention Is Associated with Improved Motor, Gut-Related, and L-DOPA-Related Outcomes in a Rat Model of Parkinson’s Disease

HY. Huang, TH. Yeh, SP. Tsao, DY. Wang, TJ. Chen (Taipei City, Taiwan)
Processing Speed across Huntington’s Disease Stages and its association with Striatal PDE10A Density

C. Madrigal Esquivel, A. Rangel Cristales, A. Wood, F. Turkheimer, J. Badenoch, J. Valera Bermejo, J. Staunton, M. Moretto, M. Veronese, M. Hartmann, N. Martin, N. Palasits, O. Makos, P. Eze, P. Tall, S. Williams, D. van Wamelen (London, United Kingdom)
Prodromal Parkinson’s Disease in Singapore: Motor and Non-Motor Symptom Patterns

R. Chen, Y. Nah, S. Ng, R. Hoe, E. Tan, Z. Xu, L. Tan (Singapore, Singapore)
Prognostic Factors for Survival in Multiple System Atrophy: A Retrospective Cohort Study with Focus on Surgical Interventions

H. Shimizu, T. Yamamoto, Y. Takahashi (Kodaira, Tokyo, Japan)
Prognostic Impact of GBA Variants on Mortality in Parkinson’s Disease: A Systematic Review and Meta-Analysis

N. Chan, A. Raphael, J. Kim, A. Haryanto, T. Khoo (Southport, Australia)
Progression and disability in Parkinson’s disease: what else can be done?

S. Shtaimets, а. Agasheva, I. Zhukova, D. Novotnyy, N. Zhukova (Tomsk, Russian Federation)
Progressive Dynamic Functional Network Disorganisation and its Association with Phenoconversion in Isolated REM Sleep Behaviour Disorder: A Multicentre Study

L. Churchill, J. Anderson, A. Ignatavicius, A. Konuri, M. Johansson, R. Gaurav, S. Lehéricy, S. Lewis, E. Matar (Sydney, Australia)
Progressive Lifelong Chorea with Spastic Paraparese and Cerebellar Ataxia Associated with Two Heterozygous Variants in the SYNE1 Gene: A Case Report

I. Sarac, H. Sarac, F. Borovecki, N. Henigsberg (Zagreb, Croatia)

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