Parallel Session 4417
Genetics: New Therapeutics and Treatments
Wednesday, October 7, 2026
14:00 - 15:30 | Conference Room North 203, Level 2
In this session we will review novel therapeutic approaches to movement disorders using genetic interventions. Specifically, we will review RNA interference (RNAi) interventions, antisense oligonucleotides (ASO) and gene editing.
Chairs:
Roy Alcalay, Israel
Christine Klein, Germany
Presenters:
RNA Interference (RNAi) Interventions
Nurit Omer, Israel
Antisense Oligonucleotides (ASO)
Jinkuk Kim, Korea
Gene Editing and Gene Replacement
Manju Kurian, United Kingdom
CSPC Liaison(s):
Roy Alcalay, Israel
Learning Objectives
At the conclusion of this session, participants should be better able to:
- Describe the mechanism of RNAi and the latest trials in Huntington’s, Parkinson’s and other movement disorders
- Describe the mechanism of ASO and the latest in common and rare movement disorders
- Describe existing therapies and experimental therapies modifying and editing genes
Recommended Audience
Clinician / General Neurology
Fellow / Resident / Student
Industry
Researcher / Basic Science
Education Level
Advanced / Expert
Intermediate / Experienced