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Osteopenia and vitamin D deficiency in children with sickle cell disease
European Journal of Haematology, 09/15/09
Chapelon E et al. – A slight BMD decrease was found in SCD children, starting before puberty and being more marked in females. The decrease was unrelated to disease severity, vitamin D deficiency, or bone hyperresorption, suggesting abnormal bone formation as the underlying mechanism.
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Predictors of response to immunosuppressive therapy with antithymocyte globulin and cyclosporine and prognostic factors for survival in patients with severe aplastic anemia
European Journal of Haematology, 12/10/09
Alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene
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