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Krivic et al., 2008) ligament-healing (Sebecic et al., 1999) (and in other models, such as is observed with rat femoral head osteonecrosis (Keremi et al., 2009)
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In sickle-cell diseases (SCD), in which hemolysis is dominant compared with dyserythropoiesis, the ERFE and GDF15 levels and their correlation with hepcidin levels were not comparable to those observed in β-thalassemia [13]
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