Determinants of Red Cell Survival and Erythropoietic Activity in Patients with Sickle Cell Anemia in the Steady State
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630260008993134
Reference27 articles.
1. Fetal Haemoglobin in Homozygous Sickle Cell Disease
2. Concurrent Sickle-Cell Anemia and α-Thalassemia
3. O-Thalassemia Reduces the Hemolytic Rate in Homozygous Sickle-Cell Disease
4. Rheologic predictors of the severity of the painful sickle cell crisis
5. Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemia
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