Transfusion in sickle cell anemia revisited
Author:
Publisher
Wiley
Subject
Hematology,Immunology,Immunology and Allergy
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1537-2995.2009.02153.x/fullpdf
Reference11 articles.
1. Gene mutation in human hemoglobin: the chemical difference between normal and sickle cell hemoglobin;Ingram;Nature,1957
2. 2. WHO. 59th World Health Assembly A59/9 Provisional agenda item 11.4. Sickle-cell anaemia: Report by the Secretariat 24 April 2006.
3. Mechanisms of disease: pulmonary complication of sickle cell disease;Gladwin;N Engl J Med,2008
4. Human Genome Epidemiology (HuGE) reviews. Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review;Ashley-Koch;Am J Epidemiol,2000
5. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The Preoperative Transfusion in Sickle Cell Disease Study Group;Vichinsky;N Engl J Med,1995
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1. Acute chest syndrome in sickle cell disease patients: Experience from a resource constrained setting;Iraqi Journal of Hematology;2019
2. Limited Exchange Transfusion Can Be Very Beneficial in Sickle Cell Anemia with Acute Chest Syndrome: A Case Report from Tanzania;Case Reports in Hematology;2018-06-21
3. Anesthetic and Cardiopulmonary Bypass Considerations for Cardiac Surgery in Unique Pediatric Patient Populations: Sickle Cell Disease and Cold Agglutinin Disease;World Journal for Pediatric and Congenital Heart Surgery;2011-07
4. Inositol hexaphosphate-loaded red blood cells prevent in vitro sickling;Transfusion;2010-05-04
5. Therapeutische Hämapherese;Transfusionsmedizin und Immunhämatologie;2010
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