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Integrative approaches to treating pain in sickle cell disease: pre-clinical and clinical evidence
Sickle cell disease (SCD) is a genetic disorder characterized by hemolysis, end-organ damage, inflammation, and pain. Recurrent and unpredictable episodes of acute pain due to vaso-occlusive crises are a unique feature of SCD. Many patients also develop lifelong chronic pain. Opioids are the primary...
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| Publicado no: | Complement Ther Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7306403/ https://ncbi.nlm.nih.gov/pubmed/32507420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ctim.2020.102394 |
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