Evaluation of bone mineral density in patients with hemoglobin H disease

Author:

Zarei Tahereh,Haghpanah Sezaneh,Parand Shirin,Moravej Hossein,Dabbaghmanesh Mohammad Hossein,Omrani Gholamhossein Ranjbar,Karimi Mehran

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference26 articles.

1. Steinberg MH, Forget BG, Higgs D R, Nagel RL (2001) Molecular mechanisms of a-thalassemia. Disorders of hemoglobin: Genetics, pathophysiology, and clinical management. Cambridge University Press 405–430

2. Laosombat V, Viprakasit V, Chotsampancharoen T, Wongchanchailert M, Khodchawan S, Chinchang W, Sattayasevana B (2009) Clinical features and molecular analysis in Thai patients with HbH disease. Ann Hematol 88(12):1185–1192

3. Fucharoen S, Winichagoon P (2012) New updating into hemoglobinopathies. Int J Lab Hematol 34(6):559–565

4. Fucharoen S, Viprakasit V (2009) Hb H disease: clinical course and disease modifiers. ASH Education Program Book 2009(1):26–34

5. Chui DH, Fucharoen S, Chan V (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101(3):791–800

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