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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

267 related items for PubMed ID: 7771550

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  • 24. The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization?
    Embury SH.
    Ann N Y Acad Sci; 1985; 445():37-44. PubMed ID: 3893275
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  • 25. [Diabetes and heterozygotic sickle-cell anemia: study of erythrocyte deformability].
    Abadie E, Fisch A.
    Pathol Biol (Paris); 1984 Apr; 32(4):256-9. PubMed ID: 6718066
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  • 27. Beyond hemoglobin polymerization: the red blood cell membrane and sickle disease pathophysiology.
    Hebbel RP.
    Blood; 1991 Jan 15; 77(2):214-37. PubMed ID: 1985689
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  • 30. Membrane-bound hemoglobin in the erythrocytes of sickle cell anemia.
    Sears DA, Luthra MG.
    J Lab Clin Med; 1983 Nov 15; 102(5):694-8. PubMed ID: 6631167
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  • 33. Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration.
    Evans E, Mohandas N, Leung A.
    J Clin Invest; 1984 Feb 15; 73(2):477-88. PubMed ID: 6699172
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  • 34. Influence of plasma and red cell factors on the rheologic properties of oxygenated sickle blood during clinical steady state.
    Morris CL, Gruppo RA, Shukla R, Rucknagel DL.
    J Lab Clin Med; 1991 Oct 15; 118(4):332-42. PubMed ID: 1940575
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  • 38. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.
    Pediatr Res; 1976 Jun 15; 10(6):613-20. PubMed ID: 1272638
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  • 39. The interaction of alpha-thalassemia and homozygous sickle-cell disease.
    Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, Grandison Y, Lowrie Y, Mason KP, Serjeant BE, Serjeant GR.
    N Engl J Med; 1982 Jun 17; 306(24):1441-6. PubMed ID: 6176865
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