Oxidative stress status, clinical outcome, and β-globin gene cluster haplotypes in pediatric patients with sickle cell disease-Reference-Cited by-同舟云学术

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Oxidative stress status, clinical outcome, and β-globin gene cluster haplotypes in pediatric patients with sickle cell disease

Published:2010-11-11 Issue:6 Volume:85 Page:529-537
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Rusanova Iryna,Escames Germaine,Cossio Gladys,De Borace Rosaura G.,Moreno Belgica,Chahboune Mariam,López Luís C.,Díez Tomas,Acuña-Castroviejo Dario

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2010.01528.x/fullpdf

Reference55 articles.

1. Sickle cell anemia, genetic variations and the trade to the United States;Schroeder;J Afr Hist,1990

2. World Health Organization 59th World Health Assembly, A59/9. Sickle Cell Anemia: Report of the Secretariat 2006

3. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells;Ballas;Am J Hematol,1991

4. Are there clinical phenotypes of homozygous sickle cell disease?;Alexander;Br J Haematol,2004

5. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes;Kato;Blood Rev,2007

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