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Journal Abstract Search
221 related items for PubMed ID: 2605778
21. Hemoglobin S levels in sickle cell trait individuals. Cameron BF, Smith DB, Cody B. Am J Hematol; 1984 Feb; 16(2):123-7. PubMed ID: 6695914 [Abstract] [Full Text] [Related]
22. Blood-oxygen affinity and sickling in sickle cell disease: effect of prior deoxygenation. Sinet M, Pocidalo JJ. J Lab Clin Med; 1981 Oct; 98(4):492-9. PubMed ID: 6793678 [Abstract] [Full Text] [Related]
23. Sickle cell disease: the proportion of liganded haemoglobin needed to prevent crises. Franklin IM, Rosemeyer MA, Huehns ER. Br J Haematol; 1983 Aug; 54(4):579-87. PubMed ID: 6871109 [Abstract] [Full Text] [Related]
24. Sickle cell trait and aviation. Long ID. Aviat Space Environ Med; 1982 Oct; 53(10):1021-9. PubMed ID: 6184047 [Abstract] [Full Text] [Related]
25. Oxygen-dependent flow of sickle trait blood as an in vitro therapeutic benchmark for sickle cell disease treatments. Lu X, Chaudhury A, Higgins JM, Wood DK. Am J Hematol; 2018 Oct; 93(10):1227-1235. PubMed ID: 30033564 [Abstract] [Full Text] [Related]
26. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene. Wong SC, Ali MA, Boyadjian SE. Acta Haematol; 1981 Oct; 65(3):157-63. PubMed ID: 6165216 [Abstract] [Full Text] [Related]
32. Glycosylated hemoglobin in Saudi sickle cell patients with glucose-6-phosphate dehydrogenase deficiency. Alayash AI, Dafallah A, Wilson MT. Acta Haematol; 1987 Apr; 78(1):54-6. PubMed ID: 3116811 [Abstract] [Full Text] [Related]
33. The Natural History of Hb S/Hereditary Persistence of Fetal Hemoglobin in 13 Children from the State of Minas Gerais, Brazil. Belisário AR, Sales RR, Silva CM, Velloso-Rodrigues C, Viana MB. Hemoglobin; 2016 Jun; 40(3):215-9. PubMed ID: 27117574 [Abstract] [Full Text] [Related]
34. Regional and temporal variation in oscillatory blood flow in sickle cell disease. Kennedy AP, Williams B, Meydrech EF, Steinberg MH. Am J Hematol; 1988 Jun; 28(2):92-4. PubMed ID: 2969189 [Abstract] [Full Text] [Related]
35. Sparing effect of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S at physiologic ligand saturations. Poillon WN, Kim BC, Rodgers GP, Noguchi CT, Schechter AN. Proc Natl Acad Sci U S A; 1993 Jun 01; 90(11):5039-43. PubMed ID: 7685112 [Abstract] [Full Text] [Related]
36. The clinical pathophysiology of sickle cell disease. Embury SH. Annu Rev Med; 1986 Jun 01; 37():361-76. PubMed ID: 2423018 [Abstract] [Full Text] [Related]
37. The relationship between fetal hemoglobin level and glycosylation in sickle cell disease. Elseweidy MM, Abraham EC. Am J Hematol; 1984 May 01; 16(4):375-81. PubMed ID: 6202137 [Abstract] [Full Text] [Related]
38. The proportion of Hb A2 is higher in sickle cell trait than in normal homozygotes. Whitten WJ, Rucknagel DL. Hemoglobin; 1981 May 01; 5(4):371-8. PubMed ID: 6788729 [Abstract] [Full Text] [Related]
39. Methods for the study of sickling and hemoglobin S gelation. Nagel RL, Chang H. Methods Enzymol; 1981 May 01; 76():760-92. PubMed ID: 7329289 [No Abstract] [Full Text] [Related]
40. Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin. Shokrani M, Terrell F, Turner EA, Aguinaga MD. Ann Clin Lab Sci; 2000 Apr 01; 30(2):191-4. PubMed ID: 10807164 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]