Iron overload after complement inhibitor treatment of Paroxysmal Nocturnal Hemoglobinuria
Author:
Affiliation:
1. Massachusetts General Hospital, Harvard Medical School Boston Massachusetts USA
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.26187
Reference6 articles.
1. Paroxysmal nocturnal hemoglobinuria
2. Abnormalities of PIG-A Transcripts in Granulocytes from Patients with Paroxysmal Nocturnal Hemoglobinuria
3. Effect of Eculizumab on Hemolysis and Transfusion Requirements in Patients with Paroxysmal Nocturnal Hemoglobinuria
4. Ravulizumab (ALXN1210) vs eculizumab in C5-inhibitor–experienced adult patients with PNH: the 302 study
5. Complement fraction 3 binding on erythrocytes as additional mechanism of disease in paroxysmal nocturnal hemoglobinuria patients treated by eculizumab
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1. Paroxysmal nocturnal hemoglobinuria: Review of the patient experience and treatment landscape;Blood Reviews;2023-11
2. Biomarkers and laboratory assessments for monitoring the treatment of patients with paroxysmal nocturnal hemoglobinuria: Differences between terminal and proximal complement inhibition;Blood Reviews;2023-05
3. Effect of Eculizumab on Iron Metabolism in Transfusion-independent Patients With Paroxysmal Nocturnal Hemoglobinuria;HemaSphere;2023-04-19
4. Paroxysmal nocturnal hemoglobinuria: Where are we going;American Journal of Hematology;2023-03-31
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