Age-dependent changes in the membrane surface area: sickle red blood cell volume may account for differential clinical effects of coinherited α thalassemia on sickle cell anemia
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2011.01743.x/fullpdf
Reference12 articles.
1. The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score;Joly;Eur J Haematol,2012
2. Concurrent sickle-cell anemia and a-thalassemia: effect on severity of anemia;Embury;N Engl J Med,1982
3. Concurrent sickle cell anemia and a thalassemia: effect on pathological properties of sickle red cells;Embury;J Clin Invest,1984
4. Monovalent cation changes in sickle erythrocytes: a direct reflection of a-globin gene number;Embury;J Lab Clin Med,1985
5. Association between morphologic distortion of sickle cells and deoxygenation-induced cation permeability increase;Mohandas;Blood,1986
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1. Females of HbAS genotype have reduced concentration of the malaria protective deoxyhemoglobin S than males;PLOS ONE;2018-09-11
2. An age dependent response to hydroxyurea in pediatric sickle cell anemia patients with alpha thalassemia trait;Blood Cells, Molecules, and Diseases;2017-07
3. The Co-Inheritance of Alpha-Thalassemia and Sickle Cell Anemia Is Associated with Better Hematological Indices and Lower Consultations Rate in Cameroonian Patients and Could Improve Their Survival;PLoS ONE;2014-06-30
4. Alpha-thalassaemia and response to hydroxyurea in sickle cell anaemia;European Journal of Haematology;2014-01-30
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