Severe Aplastic Anemia and PNH
Author:
Funder
European Society for Blood and Marrow Transplantation
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-030-02278-5_77
Reference41 articles.
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2. Bacigalupo A, Socié G, Hamladji RM, et al. Current outcome of HLA identical sibling versus unrelated donor transplants in severe aplastic anemia: an EBMT analysis. Haematologica. 2015;100:696–702.
3. Barone A, Lucarelli A, Onofrillo D, et al. Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP). Blood Cells Mol Dis. 2015;55:40–7.
4. Brodsky RA, Young NS, Antonioli E, et al. Multicenter phase III study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria. Blood. 2008;114:1840–7.
5. Camitta BM, Thomas ED, Nathan DG, et al. Severe aplastic anemia: a prospective study of the effect of early marrow transplantation on acute mortality. Blood. 1976;48:63–70.
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1. Ahemolytic PNH (white cell PNH): Clinical features and implications of a distinct phenotype of paroxysmal nocturnal haemoglobinuria;British Journal of Haematology;2024-03-12
2. Guidelines for the diagnosis and management of adult aplastic anaemia: A British Society for Haematology Guideline;British Journal of Haematology;2024-01-21
3. Relapse and transformation to myelodysplastic syndrome and acute myeloid leukemia following immunosuppressive therapy for aplastic anemia is more common as compared to allogeneic stem cell transplantation with a negative impact on survival;Annals of Hematology;2024-01-20
4. Recent advances in the diagnosis and treatment of pediatric acquired aplastic anemia;International Journal of Hematology;2023-03-03
5. Clonality in immune aplastic anemia: Mechanisms of immune escape or malignant transformation;Seminars in Hematology;2022-07
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