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Transition from pediatric to adult care for sickle cell disease: Results of a survey of pediatric providers
As recently as the 1970s, children born with sickle cell disease (SCD) were unlikely to survive into adulthood. With advances in medical care, most patients now survive childhood and live into their forties or beyond [1,2]. A better transition from pediatric- to adult-focused care is therefore incre...
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| Udgivet i: | Am J Hematol |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2011
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5804481/ https://ncbi.nlm.nih.gov/pubmed/21594889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajh.22016 |
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