The Sub-Phenotypes of Sickle Cell Disease in Kuwait
Author:
Affiliation:
1. Department of Pediatrics, Faculty of Medicine, Kuwait University, Safat, Kuwait;
2. Pediatric Hematology Unit, Mubarak Al-Kabeer Hospital, Jabriya, Kuwait;
3. Department of Pathology, Faculty of Medicine, Kuwait University, Jabriya, Kuwait
Funder
Advancement of Science
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
https://www.tandfonline.com/doi/pdf/10.1080/03630269.2019.1610427
Reference33 articles.
1. Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
2. The Clinical Sequelae of Intravascular Hemolysis and Extracellular Plasma Hemoglobin
3. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
4. Heme-induced cell adhesion in the pathogenesis of sickle-cell disease and inflammation
5. Genetic Etiologies for Phenotypic Diversity in Sickle Cell Anemia
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