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Journal Abstract Search

171 related items for PubMed ID: 132357

  • 1. Hemolytic disorders associated with a primary red cell membrane defect.
    Condrea E.
    Experientia; 1976 May 15; 32(5):537-42. PubMed ID: 132357
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  • 5. THE ROLE OF LYSOPHOSPHATIDES AND FATTY ACIDS IN HAEMOLYSIS. (A CONCEPTUAL REVIEW).
    JEANNET M, HAESSIG A.
    Vox Sang; 1964 May 15; 9():113-27. PubMed ID: 14147557
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  • 6. Red cell membrane skeletal defects in hereditary and acquired hemolytic anemias.
    Palek J, Lux SE.
    Semin Hematol; 1983 Jul 15; 20(3):189-224. PubMed ID: 6353590
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  • 8. Pathological alterations of cation movements in red blood cells.
    Parker JC, Welt LG.
    Arch Intern Med; 1972 Feb 15; 129(2):320-32. PubMed ID: 4258090
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  • 9. Surface properties of erythrocytes: normal, paroxysmal nocturnal hemoglobinuria and glutathione-treated cells.
    Atlas SJ, Shapiro B, Green JW.
    Biochim Biophys Acta; 1973 Oct 11; 323(2):194-206. PubMed ID: 4752282
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  • 10. The red cell membrane in hemolytic anemia.
    Cooper RA, Shattil SJ.
    Mod Treat; 1971 May 11; 8(2):329-51. PubMed ID: 4940517
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  • 12. Relative deficiency of Ca2 plus-dependent adenosine triphosphatase activity of red cell membranes in hereditary spherocytosis.
    Feig SA, Guidotti G.
    Biochem Biophys Res Commun; 1974 May 20; 58(2):487-94. PubMed ID: 4276124
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  • 15. Membrane ATP and the functional organization of the red cell Na:K pump.
    Hoffman JF, Proverbio F.
    Ann N Y Acad Sci; 1974 May 20; 242(0):459-60. PubMed ID: 4279598
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  • 18. Erythrocyte ion transport defects and hemolytic anemia: "hydrocytosis" and "desiccytosis".
    Nathan DG, Shohet SB.
    Semin Hematol; 1970 Oct 20; 7(4):381-408. PubMed ID: 5473420
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