Investigators Workshop | Disorders of GABA Metabolism
Sunday, December 5, 2021
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OVERVIEW:
This session examines the breakthrough approach of personalized targeted therapies for inherited metabolic epilepsies.
Personalized targeted therapies (e.g. antisense oligonucleotides, enzyme replacement, and gene therapy) are burgeoning in rare genetic-metabolicepilepsies. e.g. Inherited neurotransmitter disorders are a model for such interventions.
This workshop reviews:
- Clinical and scientific aspects of the major disorders of GABA metabolism
- Results and challenges of the recent clinical trial held at NINDS/NIH utilizing a GABA(B) receptor antagonist
- Focus on neurophysiologic strategies utilizing TMS, hdEEG, and MEG to model GABA metabolism
- Development of enzyme replacement therapy in a tetracycline-derived animal model will be illustrated as a breakthrough approach in the treatment of this and related inherited metabolic epilepsies.
Learning Objectives:
Following participation in this activity, participants will be able to:
- Develop clinical trials in rare inherited neurometabolic epilepsies
- Formulate neurophysiologic markers of neurotransmitter metabolism using EEG and MEG studies
- Learn genetically programmed on-demand models to provide enzyme replacement therapy
Program:
Moderators: Phillip L. Pearl, MD, FAES and William H. Theodore, MD, FAES
Speakers: John Schreiber, MD, Christos Papadelis, PhD, and Henry HC Lee, PhD
Education Credit:
1.5 Nursing Contact Hours
1.5 Pharmacy Contact Hours
1.5 CME