Proposals for Classification of the Clinical Stages, Grading of Severity and the Molecular Pathogenesis of Paroxysmal Nocturnal Hemoglobinuria
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Publisher
Springer Japan
Link
http://link.springer.com/content/pdf/10.1007/978-4-431-67867-0_5.pdf
Reference64 articles.
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2. Rosse WF, Dacie JV (1966) Immune lysis of normal human and paroxysmal nocturnal hemoglobinuria (PNH) red blood cells. I. The sensitivity of PNH red cells to lysis by complement and specific antibody. J Clin Invest 45: 736–748
3. Aster RH, Enright SE (1969) A platelet and granulocyte membrane defect in paroxysmal nocturnal hemoglobinuria: usefulness for the detection of platelet antibodies. J Clin Invest 48: 1199–1210
4. Dessypris EN, Clark DA, McKee LC, et al (1983) Increased sensitivity to complement of erythroid and myeloid progenitors in paroxysmal nocturnal hemoglobinuria. N Engl J Med 309: 690–693
5. Shichishima T, Terasawa T, Uchida T, et al (1989) Complement sensitivity of erythroblasts and erythropoietic precursors in paroxysmal nocturnal haemoglobinuria (PNH). Br J Haematol 72: 578–583
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