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Complications of Transfusion-Dependent β-Thalassemia Patients in Sistan and Baluchistan, South-East of Iran

Background: Thalassemia syndromes are among prevalent hereditary disorders imposing high expenses on health-care system worldwide and in Iran. Organ failure represents a life-threatening challenge in transfusion- dependent β-thalassemia (TDT) patients. The purpose of the present study was to determi...

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Bibliografski detalji
Izdano u:Int J Hematol Oncol Stem Cell Res
Glavni autori: Yaghobi, Maryam, Miri-Moghaddam, Ebrahim, Majid, Naderi, Bazi, Ali, Navidian, Ali, Kalkali, Asiyeh
Format: Artigo
Jezik:Inglês
Izdano: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017
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Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5767285/
https://ncbi.nlm.nih.gov/pubmed/29340121
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