Mycobacterium avium Complex Infection in a Patient with Sickle Cell Disease and Severe Iron Overload by Kamal Shemisa, Nasima Jafferjee, David Thomas, Gretta Jacobs, Howard J. Meyerson

“…High dietary iron, genetic defects in iron trafficking, as well as hemoglobinopathy are believed to be the etiologies for iron overload in this region. …”
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Bone Mineral Density in Thalassemia Major Patients from Antalya, Turkey by Ibrahim Aslan, Duran Canatan, Nihal Balta, Gulizar Kacar, Cengaver Dorak, Ahmet Ozsancak, Nurgul Oguz, Ruya Cosan

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Phytochemical components and antibacterial activity of two populations of Senecio vulgaris L. essential oils as traditional medicine plant by Fatemeh Hajmoradi, Hamed Fathi, Foozieh Moghadami

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Is Hydroxyurea Treatment Changing the Life of Children with Sickle Cell Disease? by Mohammed Ali Al Sabbah, Mahmoud Radaideh, Shafeeka Mohammed Saleh, Sura Ahmed Al-Doory, Amal Mahmoud Abdalqader, Fatima Farid Mir, Aya Mohammed

“…Background: Sickle cell disease (SCD) is a prevalent hemoglobinopathy involving sickled hemoglobin that causes multiorgan disease due to chronic recurrent vaso-occlusion and hemolysis. …”
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Overexpression of MiR-183/96/182 Triggers Retina-Like Fate in Human Bone Marrow-Derived Mesenchymal Stem Cells (hBMSCs) in Culture by Mohammad-Reza Mahmoudian-Sani, Fatemeh Forouzanfar, Samira Asgharzade, Nilufar Ghorbani

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Clinical Study of Mobile Application- (App-) Based Family-Centered Care (FCC) Model Combined with Comprehensive Iron Removal Treatment in Children with Severe Beta Thalassemia by Yuke Chen, Xiuping Huang, Qingmei Lu, Jian Lu, Xiaoxiao Huang, Yanni Luo, Fengxing Huang

“…Background and Objective. Hemoglobinopathy is one of the most prevalent monogenic disorders in the world. …”
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