hemoglobinuria

n.

血红素尿，血色蛋白尿；

Natural history of paroxysmal nocturnal hemoglobinuria
Isolation and characterization of a membrane protein from normal human erythrocytes that inhibits reactive lysis of the erythrocytes...
Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinu...
Distribution of decay-accelerating factor in the peripheral blood of normal individuals and patients with paroxysmal nocturnal hemog...
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria.
Mitochondrial free radical production induces lipid peroxidation during myohemoglobinuria.
Glycosylphosphatidylinositol-anchor-deficient mice: implications for clonal dominance of mutant cells in paroxysmal nocturnal hemogl...
Resistance to Apoptosis Caused by PIG-A Gene Mutations in Paroxysmal Nocturanal Hemoglobinuria
Clinical significance of a minor population of paroxysmal nocturnal hemoglobinuria-type cells in bone marrow failure syndrome.
Targeted deletion of the CD59 gene causes spontaneous intravascular hemolysis and hemoglobinuria