The Prevalence of Avascular Necrosis in Sickle Cell Anemia: Correlation with α-Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268908998842
Reference12 articles.
1. Concurrent Sickle-Cell Anemia and α-Thalassemia
2. The Interaction of Alpha-Thalassemia and Homozygous Sickle-Cell Disease
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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2. Determinants of severity in sickle cell disease;Blood Reviews;2022-11
3. The pleiotropic effects of α‐thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co‐transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival;American Journal of Hematology;2022-07-18
4. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort;Annals of Hematology;2021-02-13
5. How I treat acute and persistent sickle cell pain;Mediterranean Journal of Hematology and Infectious Diseases;2020-08-29
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