Protein Z and Endothelin-1 genetic polymorphisms in pediatric Egyptian sickle cell disease patients

Author:

Khorshied Mervat M.1ORCID,Mohamed Nohair S.1,Hamza Rania S.1,Ali Rasha M.1,El-Ghamrawy Mona K.2

Affiliation:

1. Department of Clinical and Chemical Pathology; Faculty of Medicine; Cairo University; Cairo Egypt

2. Department of Pediatrics; Faculty of Medicine; Cairo University; Cairo Egypt

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Reference31 articles.

1. Haptoglobin: an emerging candidate for phenotypic modulation of sickle cell anemia?;Santos;Rev Bras Hematol Hemoter,2015

2. Role of the hemostatic system on sickle cell disease pathophysiology and potential therapeutics;Pakbaz;Hematol Oncol Clin North Am,2014

3. Endothelin-1 but not endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease in Africa;Thakur;Gene Regul Syst Bio,2014

4. Biomarkers in sickle cell disease;Rees;Br J Haematol,2012

5. Protein Z, a protein seeking a pathology;Vasse;Thromb Haemost,2008

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