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TREAT-NMD

TREAT-NMD

Advancing diagnosis, care and treatment for people with neuromuscular diseases around the world

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TREAT-NMD’s E-Learning Platform Recognised For Positive Impact

TREAT-NMD were honoured to be shortlisted as finalists in the TalentLMS Training Excellence Awards – Positive Impact Award category! The judges recognised that our LMS training programmes have had a […]

24 November 2023

ClinGen Needs Assessment Survey

TREAT-NMD would like to share a needs assessment survey on behalf of Dr. William Craigen and Dr. Rong Mao, the Metabolism Work Group Co-Chairs for the Clinical Genome Resource The National […]

10 November 2023

TREAT-NMD Annual Curators Meeting

Photo from last year's ACM which was in Vancouver, Canada

We are looking forward to hosting TREAT-NMD Annual Curators Meeting (ACM) which is being held over two days from Monday the 4th of December to Tuesday the 5th of December […]

31 October 2023

New course now available on TREAT-NMD’s E-learning platform!

We are delighted to announce a new course is now available on TREAT-NMD’s free e-learning platform! Pre-Clinical Insights into Congenital Myopathies,  presented by Ricardo A. Galli, a PhD Candidate from […]

30 October 2023

Project Mercury and TREAT-NMD

Project Mercury is a collaborative effort established by the FSHD Society. The project brings together stakeholders from around the world to address the challenges that can slow the provision of […]

26 October 2023

Applications Now Open for Duchenne Patient Academy 2023

Applications have now been opened for the Duchenne patient academy 2023. The Duchenne Patient Academy is a unique opportunity for motivated patient advocates to receive intensive training on key aspects […]

19 October 2023
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  • Home
  • Who We Are
    • About Us
    • Partnerships and Collaborations
    • Governance
    • Our Team
    • Back
  • Who We Support
    • Patients
    • Clinicians / Researchers
    • Life Sciences Industry
    • Back
  • What We Do
    • Advisory Committee for Therapeutics
      • Members of the Advisory Committee for Therapeutics
      • Take Part in TACT
      • Past Applicants
      • Back
    • The Global Registry Network
      • Members of the Registry Network
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    • Core Datasets
      • DM dataset
      • DMD dataset
      • FSHD dataset
      • LGMD
      • SMA
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    • Education
      • Masterclasses
      • E-learning Platform
      • Endorsement of External Programmes
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    • Post-Marketing Surveillance
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  • 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
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    • Research Overview
      • DMD
        • Gene Therapy for DMD
        • Mutation Specific Approaches
        • Cell Therapy
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    • Standards of Care & Family Guides
      • CM Care
      • CMD Care
      • DM Care
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    • SOP Library
      • MDX Mouse (DMD)
      • GRMD Dog (DMD)
      • CMD Mouse (CMD)
      • SMA Mouse (SMA)
      • CMD animal models
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      • Cell Lines
        • Clinical Outcome Measures
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        • NMR (MRI/MRS) Imaging
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