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Targeting pain at its source in sickle cell disease
Sickle cell disease (SCD) is a genetic disorder associated with hemolytic anemia, end-organ damage, reduced survival, and pain. One of the unique features of SCD is recurrent and unpredictable episodes of acute pain due to vasoocclusive crisis requiring hospitalization. Additionally, patients with S...
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| Publicado no: | Am J Physiol Regul Integr Comp Physiol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Physiological Society
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6087885/ https://ncbi.nlm.nih.gov/pubmed/29590553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpregu.00021.2018 |
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