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2. Phosphatidylserine externalization in sickle red blood cells: associations with cell age, density, and hemoglobin F. Yasin Z; Witting S; Palascak MB; Joiner CH; Rucknagel DL; Franco RS Blood; 2003 Jul; 102(1):365-70. PubMed ID: 12609840 [TBL] [Abstract][Full Text] [Related]
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11. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease. Maier-Redelsperger M; Noguchi CT; de Montalembert M; Rodgers GP; Schechter AN; Gourbil A; Blanchard D; Jais JP; Ducrocq R; Peltier JY Blood; 1994 Nov; 84(9):3182-8. PubMed ID: 7524767 [TBL] [Abstract][Full Text] [Related]
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14. Fetal hemoglobin in sickle cell disease: relationship to erythrocyte phosphatidylserine exposure and coagulation activation. Setty BN; Kulkarni S; Rao AK; Stuart MJ Blood; 2000 Aug; 96(3):1119-24. PubMed ID: 10910931 [TBL] [Abstract][Full Text] [Related]
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16. Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease. Marcus SJ; Kinney TR; Schultz WH; O'Branski EE; Ware RE Am J Hematol; 1997 Jan; 54(1):40-6. PubMed ID: 8980259 [TBL] [Abstract][Full Text] [Related]
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20. Two distinct pathways mediate the formation of intermediate density cells and hyperdense cells from normal density sickle red blood cells. Schwartz RS; Musto S; Fabry ME; Nagel RL Blood; 1998 Dec; 92(12):4844-55. PubMed ID: 9845552 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]