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SMA Europe launches their Call for Research nr. 12

Home / Uncategorised / SMA Europe launches their Call for Research nr. 12
SMA Europe Call for Research nr. 12

SMA Europe launches their Call for Research nr. 12

SMA Europe is a non-profit umbrella organisation of spinal muscular atrophy (SMA) patient organisations from across Europe, who work to bring effective treatments and optimal care to everyone living with SMA.

Together, through greater understanding, their aim is to create a better world for all those living with SMA.

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. In particular, priority will be given to projects concentrating on the following areas:

  • Reviving the motor unit in patients with SMA with a specific interest for the role of NMJ (dys)function (including skeletal muscle and development/developmental vulnerability of motor neurons in the spinal cord/brain stem).
  • Biomarkers within and beyond the neuromuscular system.
  • How metabolism is affected in SMA and how this might influence peripheral organs.

SMA Europe strives for earlier diagnosis, effective treatments and optimal care for people who live with SMA. They do this by elevating the patient’s voice, by empowering member organisations to advocate and campaign at a national level and through harnessing that network to advance research and influence stakeholders at European level.

For more information about the Call, the application procedure and eligibility criteria visit > SMA Europe | Our Call for Research Projects | SMA Innovation (sma-europe.eu)

 

27 March 2024

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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
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    • Conference Programme
    • Sponsors of the TREAT-NMD 8th International Conference
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