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Bloodstream infections in hospitalized adults with sickle cell disease: A retrospective analysis

✍ Scribed by Lalita Chulamokha; Stephen J. Scholand; Jeff M. Riggio; Samir K. Ballas; David Horn; Joseph A. DeSimone


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
210 KB
Volume
81
Category
Article
ISSN
0361-8609

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The clinical and biological heterogeneity of sickle cell hemoglobin (Hb) C disease (SC disease) is similar to sickle cell anemia, but has a much milder course. The effect of genetic factors such as ␣ thalassemia or ␀-globin gene haplotype has been analyzed in a limited number of cases. In this work,