Risk-adapted procedures for HSCT from alternative donor in children with severe aplastic anaemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Transplantation,Hematology
Link
http://www.nature.com/articles/bmt2008293.pdf
Reference25 articles.
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2. Kojima S, Hibi S, Kosaka Y, Yamamoto M, Tsuchida M, Mugishima H et al. Immunosuppressive therapy using antithymocyte globulin, cyclosporine, and danazol with or without human granulocyte colony-stimulating factor in children with acquired aplastic anemia. Blood 2000; 96: 2049–2054.
3. Locasciulli A, Oneto R, Bacigalupo A, Socie G, Korthof E, Bekassy A et al. Outcome of patients with acquired aplastic anemia given first line bone marrow transplantation or immunsuppressive treatment in the last decade: a report from the European Group for Blood and Marrow Transplantation. Haematologica 2007; 92: 11–18.
4. Kosaka Y, Yagasaki H, Sano K, Kobayashi R, Ayukawa H, Kaneko T et al. Prospective multicenter trial comparing repeated immunosuppressive therapy with stem cell transplantation from an alternative donor as second-line treatment for children with severe and very severe aplastic anemia. Blood 2008; 111: 1054–1059.
5. Bagby GC, Meyers G . Bone marrow failure as a risk factor for clonal evolution: prospects for leukemia prevention. Hematology AM Soc Hematol Educ Program 2007; 2007: 40–46.
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2. Hematopoietic stem cell transplantation without in vivo T-cell depletion for pediatric aplastic anemia: A single-center experience;Pediatric Transplantation;2018-05-10
3. Cotransplantation of bone marrow-derived mesenchymal stem cells in haploidentical hematopoietic stem cell transplantation in patients with severe aplastic anemia: an interim summary for a multicenter phase II trial results;Bone Marrow Transplantation;2017-01-09
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