Hematopoietic cell transplantation from related and unrelated donors after minimal conditioning as a curative treatment modality for severe paroxysmal nocturnal hemoglobinuria
Author:
Publisher
Elsevier BV
Subject
Transplantation,Hematology
Reference29 articles.
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2. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria;Takeda;Cell,1993
3. Glycosyl phosphatidylinositol (GPI)-anchored molecules and the pathogenesis of paroxysmal nocturnal hemoglobinuria;Boccuni;Crit Rev Oncol Hematol,2000
4. Natural history of paroxysmal nocturnal hemoglobinuria;Hillmen;N Engl J Med,1995
5. Paroxysmal nocturnal haemoglobinuria;Socié;Lancet,1996
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2. Hematopoietic Stem Cell Transplantation for Patients with Paroxysmal Nocturnal Hemoglobinuria with or Without Aplastic Anemia: Multicenter Turkish Experience;Turkish Journal of Hematology;2021-06-01
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