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Journal Abstract Search

86 related items for PubMed ID: 409034

  • 1. Susceptibility to autoxidation of lipids of paroxysmal nocturnal hemoglobinuria (PNH)-like red cells.
    Kalafatas P, Voulgaris E, Vorias N, Kotsifopoulos P.
    Acta Haematol; 1977; 58(3):181-8. PubMed ID: 409034
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  • 4. Characterization of the complement sensitivity of paroxysmal nocturnal hemoglobinuria erythrocytes.
    Parker CJ, Wiedmer T, Sims PJ, Rosse WF.
    J Clin Invest; 1985 Jun; 75(6):2074-84. PubMed ID: 4008653
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  • 5. Altered expression of gangliosides in erythrocytes of paroxysmal nocturnal hemoglobinuria.
    Nakakuma H, Kawaguchi T, Horikawa K, Hidaka M, Yonemura Y, Kawakita M, Kagimoto T, Iwamori M, Nagai Y, Takatsuki K.
    J Clin Invest; 1990 May; 85(5):1456-61. PubMed ID: 2185273
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  • 6. Relation between low erythrocyte acetylcholinesterase activity and membrane lipids in paroxysmal nocturnal haemoglobinuria.
    Siriwittayakorn J, Yuthavong Y.
    Br J Haematol; 1979 Mar; 41(3):383-91. PubMed ID: 427042
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  • 10. Functional study of lipids of PNH red cell membranes: susceptibility of liposomes to reactive lysis.
    Tedesco F, Kahane I, Zanella A, Giovanetti AM, Sirchia G.
    Blood; 1981 May; 57(5):900-5. PubMed ID: 7214020
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  • 11. The acetylcholinesterase defect in paroxysmal nocturnal hemoglobinuria: evidence that the enzyme is absent from the cell membrane.
    Chow FL, Telen MJ, Rosse WF.
    Blood; 1985 Oct; 66(4):940-5. PubMed ID: 4041621
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  • 12. Relations between surface charge and in vitro lysis of red blood cells in paroxysmal nocturnal haemoglobinuria.
    Hause LL, Koethe SM, Rothwell DJ, Straumfjord JV.
    Scand J Haematol; 1978 Feb; 20(2):141-6. PubMed ID: 635466
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  • 13. Erythrocyte membrane defects and asymmetry in paroxysmal nocturnal hemoglobinuria and myelodysplastic syndrome.
    Basu S, Banerjee D, Ghosh M, Chakrabarti A.
    Hematology; 2010 Aug; 15(4):236-9. PubMed ID: 20670483
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  • 15. [Paroxysmal nocturnal hemoglobinuria (PNH) deficiency of major complement-regulatory membrane proteins on erythrocytes].
    Ninomiya H, Kobayashi T, Abe T.
    Rinsho Ketsueki; 1991 Jun; 32(6):612-7. PubMed ID: 1716325
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  • 17. Complement lysis of human erythrocytes. Differeing susceptibility of two types of paroxysmal nocturnal hemoglobinuria cells to C5b-9.
    Packman CH, Rosenfeld SI, Jenkins DE, Thiem PA, Leddy JP.
    J Clin Invest; 1979 Aug; 64(2):428-33. PubMed ID: 457861
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  • 18. [Altered metabolism of membrane glycosphingolipids in erythrocytes of paroxysmal nocturnal hemoglobinuria].
    Nakakuma H, Kawaguchi T.
    Rinsho Ketsueki; 1991 Jun; 32(6):606-11. PubMed ID: 1890736
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  • 19. The mechanism of decreased red cell acetylcholinesterase activity in patients with paroxysmal nocturnal hemoglobinuria: Its relation to the membrane lipids.
    Shinohara K, Matsumoto N, Ishida Y, Kaneko T.
    Nihon Ketsueki Gakkai Zasshi; 1983 Feb; 46(1):25-9. PubMed ID: 6858569
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  • 20. Relationship between the membrane inhibitor of reactive lysis and the erythrocyte phenotypes of paroxysmal nocturnal hemoglobinuria.
    Holguin MH, Wilcox LA, Bernshaw NJ, Rosse WF, Parker CJ.
    J Clin Invest; 1989 Nov; 84(5):1387-94. PubMed ID: 2478585
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