Relapse of Aplastic Anemia with Majority Donor Chimerism (Donor-Type Aplasia) Occurring Late after Bone Marrow Transplantation
Author:
Publisher
Elsevier BV
Subject
Transplantation,Hematology
Reference28 articles.
1. Impact of age on outcomes after bone marrow transplantation for acquired aplastic anemia using HLA-matched sibling donors;Gupta;Haematologica,2010
2. Paediatric amendment to adult BSH Guidelines for aplastic anaemia;Samarasinghe;Br J Haematol,2018
3. Outcome of aplastic anaemia in children. A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant;Dufour;Br J Haematol,2015
4. First-line treatment for severe aplastic anemia in children: bone marrow transplantation from a matched family donor versus immunosuppressive therapy;Yoshida;Haematologica,2014
5. Haematopoietic stem cell transplantation for acquired aplastic anaemia;Young;Curr Opin Hematol,2013
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1. Prospects and Potential for Chimerism Analysis after Allogeneic Hematopoietic Stem Cell Transplantation;Cells;2024-06-06
2. T‐cell‐replete retransplantation in children with severe aplastic anemia who developed late graft failure;Pediatric Blood & Cancer;2023-10-17
3. Recent advances in the diagnosis and treatment of pediatric acquired aplastic anemia;International Journal of Hematology;2023-03-03
4. Stem Cell Transplant for Severe Aplastic Anemia;Basics of Hematopoietic Stem Cell Transplant;2023
5. Comparisons of unmanipulated haploidentical donor, unrelated cord blood donor and matched unrelated donor hematopoietic stem cell transplantation in pediatric acquired severe aplastic anemia: a single center study;Leukemia & Lymphoma;2022-09-06
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