Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2006.00679.x/fullpdf
Reference35 articles.
1. The Sickle Cell Painful Crisis in Adults: Phs and Objective Signs
2. Red blood cell changes during the evolution of the sickle cell painful crisis
3. Lactic Acid Dehydrogenase Activity and Plasma Hemoglobin Elevations in Sickle Cell Disease
4. Plasma Hemoglobin and Hemoglobin Fractions in Sickle Cell Crisis
5. Serum α-hydroxybutyrate dehydrogenase levels in children with sickle cell disease
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