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Application Process Closing Soon for the Expert Becker Muscular Dystrophy Masterclass, Barcelona 2023

Our new education initiative in Becker muscular dystrophy has proven very popular, but there is still time to apply!  The application process will be closing on Monday 9th October so, […]

27 September 2023

Early Diagnosis for Duchenne Muscular Dystrophy Project

Early diagnosis for Duchenne muscular dystrophy presents its own challenges in terms of both the clinical and psychosocial sphere.  In July, TREAT-NMD hosted a discussion led by Michelle Lorentzos (Paediatric […]

27 September 2023

Coalition to Cure Calpain 3 in partnership with the National Organization for Rare Disorders (NORD®) launches LGMD2A/Calpainopathy Registry

Coalition to Cure Calpain 3 (C3) in partnership with the National Organization for Rare Disorders (NORD®) has launched a study with global reach to research Calpainopathy (including limb-girdle muscular dystrophy […]

25 September 2023

CureDuchenne Launches the CureDuchenne Caregiver Course: A Free Virtual Resource for Duchenne Muscular Dystrophy Caregivers

CureDuchenne has launched a new caregiver course. This free virtual resource is designed to provide invaluable guidance and support to caregivers of individuals newly diagnosed with Duchenne muscular dystrophy and […]

21 September 2023

Upcoming ENMC Workshops

For the past three decades, the European Neuromuscular Centre (ENMC) has organised over 270 workshops, bringing together an esteemed cohort of 20-25 participants. This assembly comprises leading researchers, clinicians, dedicated […]

19 September 2023

Latest Issue of Journal of Neuromuscular Diseases Published

A new issue of Journal of Neuromuscular Diseases (JND) has been published online. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that […]

14 September 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
    • Programme Committee
    • Abstracts
    • Venue
  • News & Events
    • News
    • TREAT-NMD Events
    • All Events
    • Submit an Event
    • Newsletter Sign-up
    • Contact Us