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4. Sickle cell rheology is determined by polymer fraction--not cell morphology. Hiruma H; Noguchi CT; Uyesaka N; Hasegawa S; Blanchette-Mackie EJ; Schechter AN; Rodgers GP Am J Hematol; 1995 Jan; 48(1):19-28. PubMed ID: 7832188 [TBL] [Abstract][Full Text] [Related]
5. Hb S/Hb Lepore with mild sickling symptoms: a hemoglobin variant with mostly delta-chain sequences ameliorates sickle-cell disease. Fairbanks VF; McCormick DJ; Kubik KS; Rezuke WN; Black D; Ochaney MS; Schwartz D Am J Hematol; 1997 Feb; 54(2):164-5. PubMed ID: 9034293 [TBL] [Abstract][Full Text] [Related]
6. Effect of piracetam on sickle erythrocytes and sickle hemoglobin. Asakura T; Ohnishi ST; Adachi K; Ozguc M; Hashimoto K; Devlin MT; Schwartz E Biochim Biophys Acta; 1981 May; 668(3):397-405. PubMed ID: 7236716 [TBL] [Abstract][Full Text] [Related]
7. Altered amount and activity of superoxide dismutase in sickle cell anemia. Schacter L; Warth JA; Gordon EM; Prasad A; Klein BL FASEB J; 1988 Mar; 2(3):237-43. PubMed ID: 3350236 [TBL] [Abstract][Full Text] [Related]
8. A model for the sickle cell. I. Hemorheology and II. Microcalorimetry. Cerny LC; Cook FB; Stasiw DM Biorheology; 1974 Jul; 11(4):235-9. PubMed ID: 4447819 [No Abstract] [Full Text] [Related]
9. Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytes. Presley TD; Perlegas AS; Bain LE; Ballas SK; Nichols JS; Sabio H; Gladwin MT; Kato GJ; Kim-Shapiro DB Hemoglobin; 2010; 34(1):24-36. PubMed ID: 20113285 [TBL] [Abstract][Full Text] [Related]
10. Hemoglobin S Antilles: a variant with lower solubility than hemoglobin S and producing sickle cell disease in heterozygotes. Monplaisir N; Merault G; Poyart C; Rhoda MD; Craescu C; Vidaud M; Galacteros F; Blouquit Y; Rosa J Proc Natl Acad Sci U S A; 1986 Dec; 83(24):9363-7. PubMed ID: 3467311 [TBL] [Abstract][Full Text] [Related]
11. Sickle cell anemia as a rheologic disease. Horne MK Am J Med; 1981 Feb; 70(2):288-98. PubMed ID: 7008586 [TBL] [Abstract][Full Text] [Related]
12. Hematological findings in 375 Sicilians with Hb S trait. SchilirĂ² G; Comisi FF; Testa R; Dibenedetto SP; Samperi P; Marino S Haematologica; 1990; 75(2):113-6. PubMed ID: 2358201 [TBL] [Abstract][Full Text] [Related]
13. Detection of alpha thalassaemia in sickle cell trait patients by Hb-Bart's screening & quantitation of Hb-A & Hb-S. Misra RC Indian J Med Res; 1989 Dec; 90():459-62. PubMed ID: 2628314 [TBL] [Abstract][Full Text] [Related]
14. betaS Chain turnover in reticulocytes of sickle trait individuals with high or low concentrations of haemoglobin S. Shaeffer JR; Kleve LJ; DeSimone J Br J Haematol; 1976 Mar; 32(3):365-72. PubMed ID: 1252371 [TBL] [Abstract][Full Text] [Related]
15. Determinants of red cell sickling. Effects of varying pH and of increasing intracellular hemoglobin concentration by osmotic shrinkage. Bookchin RM; Balazs T; Landau LC J Lab Clin Med; 1976 Apr; 87(4):597-616. PubMed ID: 5563 [TBL] [Abstract][Full Text] [Related]
16. Biochemical diagnosis in sickle cell disease. Isaacs WA Ghana Med J; 1971 Mar; 10(1):40-3. PubMed ID: 5173734 [TBL] [Abstract][Full Text] [Related]
17. Modification of sickle hemoglobin by acetaldehyde and its effect on oxygenation, gelation and sickling. Abraham EC; Stallings M; Abraham A; Garbutt GJ Biochim Biophys Acta; 1982 Jul; 705(1):76-81. PubMed ID: 7115734 [TBL] [Abstract][Full Text] [Related]
18. Exercise and hypoxia increase sickling in venous blood from an exercising limb in individuals with sickle cell trait. Martin TW; Weisman IM; Zeballos RJ; Stephenson SR Am J Med; 1989 Jul; 87(1):48-56. PubMed ID: 2741981 [TBL] [Abstract][Full Text] [Related]