Late complications of mixed chimerism following allogeneic bone marrow transplantation for thalassemia major
Author:
Affiliation:
1. Memorial Sloan-Kettering Cancer Center, Department of Pediatrics; Bone Marrow Transplant Service; New York
2. New York-Presbyterian Hospital-Weill Cornell Medical College; Department of Pediatrics; New York
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Reference2 articles.
1. Long-term survival of ex-thalassemic patients with persistent mixed chimerism after bone marrow transplantation;Andreani;Bone Marrow Transplant,2000
2. Recurrence of beta-thalassemia major more than 20 years after HLA-identical sibling BMT treated successfully with donor lymphocyte infusion;Inamoto;Bone Marrow Transplant,2011
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Prediction, management, and prognosis of mixed chimerism after hematopoietic stem cell transplantation in transfusion‐dependent pediatric thalassemia patients;Pediatric Transplantation;2020-10-24
2. A Multicenter Retrospective Analysis Stressing the Importance of Long-Term Follow-Up after Hematopoietic Cell Transplantation for β-Thalassemia;Biology of Blood and Marrow Transplantation;2017-10
3. Current Results and Future Research Priorities in Late Effects after Hematopoietic Stem Cell Transplantation for Children with Sickle Cell Disease and Thalassemia: A Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects after Pediatric Hematopoietic Stem Cell Transplantation;Biology of Blood and Marrow Transplantation;2017-04
4. Allogeneic Stem Cell Transplantation in Congenital Hemoglobinopathies Using a Tailored Busulfan-Based Conditioning Regimen: Single-Center Experience;Biology of Blood and Marrow Transplantation;2016-06
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