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Red blood cell transfusion to treat or prevent complications in sickle cell disease: an overview of Cochrane reviews
BACKGROUND: Globally, sickle cell disease (SCD) is one of the commonest severe monogenic disorders, due to the inheritance of two abnormal haemoglobin (beta globin) genes. SCD can cause severe pain, significant end‐organ damage, pulmonary complications, and premature death. Red blood cell (RBC) tran...
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| Pubblicato in: | Cochrane Database Syst Rev |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley & Sons, Ltd
2018
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6513377/ https://ncbi.nlm.nih.gov/pubmed/30067867 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012082.pub2 |
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