Paroxysmal nocturnal hemoglobinuria: The biochemical defects and the clinical syndrome

Author:

Rosse W.F

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference101 articles.

1. Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor;Nicholson-Weller,1983

2. Distribution of decay accelerating factor in the peripheral blood of normal individuals and patients with paroxysmal nocturanal hemoglobinuria;Kinoshita;Journal of Experimental Medicine,1985

3. Paroxysmal nocturnal hemoglobinuria type III. Lack of an erythrocyte membrane protein restricting the lysis of C5b-9;Hansch;Journal of Clinical Investigation,1987

4. Deficiency of the homologous restriction factor in paroxysmal nocturnal hemoglobinuria;Zalman;Journal of Experimental Medicine,1987

5. Selvaraj P, Rosse W F, Silber R, Springer T A The major Fc receptor in blood has a phosphotidylinositol anchor and is deficient in paroxysmal nocturnal hemoglobinuria. Nature (in press)

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