Utility Of The Multivariate Approach In Predicting β-Thalassemia Intermedia Or β-Thalassemia Major Types In Iranian Patients

By Banan Mehdi   Bayat Hadi   Namdar-Aligoodarzi Pegah   Azarkeivan Azita   Kamali Koorosh   Daneshmand Parvaneh   Zaker-Kandjani Behzad   Najmabadi Hossein  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 413-422

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The Current Status of β-Thalassemia Major in Mainland China

By Xu Lu-Hong   Fang Jian-Pei  

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 307-314

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Effect of Antioxidant Therapy on Hepatic Fibrosis and Liver Iron Concentrations in β-Thalassemia Major Patients

By Elalfy Mohsen S.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 257-276

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Peroxisome Proliferator-Activated Receptor-γ Pro12Ala Polymorphism and Risk of Osteopenia in β-Thalassemia Major Patients

By Sahmani Mehdi   Gholami Abdollah   Azarkeivan Azita   Darabi Masoud   Ahmadi Mohammad Hossein   Sabet Majid Sirati   Najafipour Reza  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 564-573

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Annotated Definition of BCL11A and HMIP-2 Haplotypes Through the Analysis of Sicilian β-Thalassemia Patients with High Levels of Fetal Hemoglobin

By Buccheri Maria A.   Spina Sonia   Ruberto Concetta   Lombardo Turi   Labie Dominique   Ragusa and Angela  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 423-434

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