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SMA Europe launches their Call for Research nr. 12

SMA Europe Call for Research nr. 12

This new Call for SMA research projects is open to research proposals that address the needs of people who live with SMA and demonstrate a clear pathway to impacting those in the short or longer term.

27 March 2024

Applications For the Duchenne Parent Project Netherlands’ 2024 Research Grant Are Now Open!

Duchenne Parent Project Netherlands' 2024 Research Grant

The 2024 research grant presents an opportunity to shape the future landscape of Duchenne research. By funding innovative projects and fostering collaboration, Duchenne Parent Project Netherlands aims to accelerate progress towards effective treatments and therapies for Duchenne muscular dystrophy.

21 March 2024

Happy 10th Anniversary to the Journal of Neuromuscular Diseases!

10th Anniversary

The Journal of Neuromuscular Diseases celebrates its 10 year anniversary!

18 January 2024

Mark Your Calendar: Key Awareness Days for 2024 Advocacy

In a world where awareness drives change and understanding, recognising specific days dedicated to various causes can be pivotal. These dates serve as crucial platforms to spotlight issues, empower communities, […]

6 December 2023

A Few Save the Dates for 2024

Get your diaries out and make sure you pencil in the key upcoming events and conferences for the neuromuscular community for 2024 and beyond.  For a full up to date […]

6 December 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 […]

6 December 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