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From Bench to Bedside: Gene Therapy Approaches for Rare Diseases

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Gene replacement therapy is emerging as a potential treatment for rare CNS diseases. In this recorded CME satellite symposium, a parent of a child with spinal muscular atrophy describes their journey through gene therapy clinical trials. Using spinal muscular atrophy as an example, three faculty experts walk through the history of gene therapy from the bench to the bedside.

This activity is hosted on Pro-CME. By clicking Begin Activity, you will be leaving The France Foundation website. Registration on Pro-CME may be required.


Webinar | Video | Pulmonary | CME (AMA PRA Category 1 Credit) | Gastroenterology | Genetic Counselor | Internal Medicine | Neurology | Neuromuscular Specialist | Pediatrics | 1.5 - 90 mins | Nurse | Nurse Practitioner | Ob/Gyn & Women's Health | Physical Medicine & Rehabilitation | Spinal Muscular Atrophy | Genomic Medicine | Neonatal/Perinatal  | Neurosurgery | Orthopedic Surgery | 

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