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Introducing the first JND Podcast: Safety and Challenges of Gene Therapy with Carsten Bonneman

Home / Uncategorised / Introducing the first JND Podcast: Safety and Challenges of Gene Therapy with Carsten Bonneman

Introducing the first JND Podcast: Safety and Challenges of Gene Therapy with Carsten Bonneman

A series of podcasts has been initiated to delve into publications from the Journal of Neuromuscular Diseases, featuring insightful conversations with authors and investigators. The inaugural episode introduces Dr. Carsten Bönnemann, who shares updates on safety and challenges in gene transfer therapy for neuromuscular diseases. The episode also includes a discussion on the 2022 Muscular Dystrophy Association Summit’s meeting report with Dr. Grace McMacken..

Listeners can expect to gain valuable insights into the current state of gene therapy research, potential breakthroughs, and the collaborative efforts showcased at the Muscular Dystrophy Association Summit.

As the podcast series unfolds, it promises to feature more engaging discussions with experts in the field of neuromuscular diseases. By spotlighting noteworthy publications from the Journal of Neuromuscular Diseases, the series aims to keep its audience informed and inspired about the latest advancements and research shaping the future of treatment options.

You can access the podcast series on Spotify and be sure to subscribe for future episodes.

 

18 October 2023

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  • Home
  • Who We Are
    • About Us
    • Partnerships and Collaborations
    • Governance
    • Our Team
  • Who We Support
    • Patients
    • Clinicians / Researchers
    • Life Sciences Industry
  • What We Do
    • Advisory Committee for Therapeutics
      • Members of the Advisory Committee for Therapeutics
      • Take Part in TACT
      • Past Applicants
    • The Global Registry Network
      • Members of the Registry Network
    • Core Datasets
      • DM dataset
      • DMD dataset
      • FSHD dataset
      • LGMD
      • SMA
    • Education
      • Masterclasses and Events
      • Digital Resources
      • Endorsement of External Programmes
    • Post-Marketing Surveillance
  • Resources and Support
    • Neuromuscular Disease Information
      • Becker muscular dystrophy
      • Charcot-Marie-Tooth
      • Congenital muscular dystrophy
      • Congenital myasthenic syndromes
      • Duchenne muscular dystrophy
      • Facioscapulohumeral muscular dystrophy
      • GNE myopathy
      • Limb girdle muscular dystrophy
      • Myotonic dystrophy
      • Myotubular and centronuclear myopathies
      • Spinal muscular atrophy
    • Research Overview
      • DMD
        • Gene Therapy for DMD
        • Mutation Specific Approaches
        • Cell Therapy
        • Drug Therapy
    • Standards of Care & Family Guides
      • CM Care
      • CMD Care
      • DM Care
      • DMD Care
      • BMD Care
      • FSHD Care
      • SMA Care
    • SOP Library
      • MDX Mouse (DMD)
      • GRMD Dog (DMD)
      • CMD Mouse (CMD)
      • SMA Mouse (SMA)
      • CMD animal models
      • MDC1A Preclinical Research
      • Cell Lines
        • Clinical Outcome Measures
        • Functional Evaluation Tools
        • NMR (MRI/MRS) Imaging
        • Muscle Biopsy
    • Social and Ethical Issues
  • Conference
    • Registration
    • Sponsorship Opportunities
    • Conference Programme
    • Sponsors of the TREAT-NMD 8th International Conference
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