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Information Journal Paper

Title

Osteoporosis in Transfusion Dependent Thalassemia

Pages

  2-5

Keywords

Not Registered.

Abstract

 -thalassemia syndromes are the most prevalent quantitative hereditary hemoglobinopathies in the world. One of the most debilitating complications in thalassemia patients is osteoporosis and osteopenia which predisposes them to skeletal pain and pathologic fractures. Osteoporosis was more prevalent in patients with thalassemia intermedia compared to thalassemia major. . . .

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    Cite

    APA: Copy

    HASHEMIEH, MOZHGAN. (2019). Osteoporosis in Transfusion Dependent Thalassemia. ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), 22(5 ), 2-5. SID. https://sid.ir/paper/69176/en

    Vancouver: Copy

    HASHEMIEH MOZHGAN. Osteoporosis in Transfusion Dependent Thalassemia. ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ)[Internet]. 2019;22(5 ):2-5. Available from: https://sid.ir/paper/69176/en

    IEEE: Copy

    MOZHGAN HASHEMIEH, “Osteoporosis in Transfusion Dependent Thalassemia,” ARAK MEDICAL UNIVERSITY JOURNAL (AMUJ), vol. 22, no. 5 , pp. 2–5, 2019, [Online]. Available: https://sid.ir/paper/69176/en

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