Actualitat Agenda

#SeminarIRSJD · Development of gene therapies for neuromuscular diseases

Auditori J. Plaza · Hospital Sant Joan de Déu Barcelona

15:30h

  • Dra. Ana Maria Buj-Bello, investigadora convidada de l'INSERM (França).

Seminari exclusiu per personal de la institució.

Resum

Gene transfer using recombinant adeno-associated viral (AAV) vectors represents a promising approach to treat human diseases. In this presentation, I will provide an overview of our work on the development of AAV-based gene therapies for two severe pediatric diseases, X-linked myotubular myopathy (XLMTM) and spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME), and current challenges in the field.

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