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Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease
Individuals with sickle cell disease (SCD) may have oxyhaemoglobin desaturation during the steady-state, the causes of which are incompletely known. We studied a cohort of 585 children who have sickle cell anaemia (SS), sickle β(0)-thalassaemia (Sβ(0)), sickle-haemoglobin C disease (SC), or sickle β...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2005
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1866256/ https://ncbi.nlm.nih.gov/pubmed/16173973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2141.2005.05738.x |
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