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The involvement of rare disease patient organisations in therapeutic innovation across rare paediatric neurological conditions: a narrative review
Abstract Background The patient voice is becoming increasingly prominent across all stages of therapeutic innovation. It pervades research domains from funding and recruitment, to translation, care, and support. Advances in genomic technologies have facilitated novel breakthrough therapies, whose gl...
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Huvudupphovsmän: | , , , , , |
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Materialtyp: | Artigo |
Språk: | Inglês |
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BMC
2022-04-01
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Serie: | Orphanet Journal of Rare Diseases |
Ämnen: | |
Länkar: | https://doi.org/10.1186/s13023-022-02317-6 |
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