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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Detalles Bibliográficos
Autores principales: Yaghobi, Maryam, Miri-Moghaddam, Ebrahim, Majid, Naderi, Bazi, Ali, Navidian, Ali, Kalkali, Asiyeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences, Hematology-Oncology and Stem Cell Transplantation Research Center 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767285/
https://www.ncbi.nlm.nih.gov/pubmed/29340121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767285/
https://www.ncbi.nlm.nih.gov/pubmed/29340121

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