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Pharmacological interventions for painful sickle cell vaso‐occlusive crises in adults
BACKGROUND: Sickle cell disease (SCD) is a group of inherited disorders of haemoglobin (Hb) structure in a person who has inherited two mutant globin genes (one from each parent), at least one of which is always the sickle mutation. It is estimated that between 5% and 7% of the world's populati...
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| Publicado en: | Cochrane Database Syst Rev |
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| Autores principales: | , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
John Wiley & Sons, Ltd
2019
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| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6863096/ https://ncbi.nlm.nih.gov/pubmed/31742673 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012187.pub2 |
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