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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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| Pubblicato in: | Am J Physiol Regul Integr Comp Physiol |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Physiological Society
2018
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| Soggetti: | |
| Accesso online: | 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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