Quality of life in patients with transfusion-dependent thalassemia after hematopoietic SCT
Author:
Publisher
Springer Science and Business Media LLC
Subject
Transplantation,Hematology
Link
http://www.nature.com/articles/bmt2008165.pdf
Reference26 articles.
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2. Olivieri NF, Brittenham GM . Iron-chelating therapy and the treatment of thalassemia. Blood 1997; 89: 739–761.
3. Ismail A, Campbell MJ, Ibrahim HM, Jones GL . Health related quality of life in Malaysian children with thalassaemia. Health Qual Life Outcomes 2006; 4: 39.
4. Telfer P, Constantinidou G, Andreou P, Christou S, Modell B, Angastiniotis M . Quality of life in thalassemia. Ann NY Acad Sci 2005; 1054: 273–282.
5. Goldbeck L, Baving A, Kohne E . [Psychosocial aspects of beta-thalassemia: distress, coping and adherence]. Klinische Padiatrie 2000; 212: 254–259.
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2. Magnetic resonance imaging assessment of the changes of cardiac and hepatic iron load in thalassemia patients before and after hematopoietic stem cell transplantation;Scientific Reports;2023-11-10
3. Health-Related Quality-of-Life Profile of Pediatric Patients with β Thalassemia after Hematopoietic Stem Cell Transplantation;Journal of Clinical Medicine;2023-09-19
4. Thalassemia patients in transfussion dependent period and after hematopoietic stem cell transplantation: how are the psychiatric status and life quality of these patients?;Pediatric Hematology and Oncology;2023-07-30
5. Health-related quality of life among thalassemia patients in Bangladesh using the SF-36 questionnaire;Scientific Reports;2023-05-12
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