[1]Shin DH, Kim HS, Park MJ, et al. Utility of access soluble transferrin receptor (sTfR) and sTfR/log ferritin index in diagnosing iron deficiency anemia[J]. Ann Clin Lab Sci, 2015, 45:396-402. [2]Skikne BS, Punnonen K, Caldron PH, et al. Improved differential diagnosis of anemia of chronic disease and iron deficiency anemia: a prospective multicenter evaluation of soluble transferrin receptor and the sTfR/log ferritin index[J]. Am J Hematol, 2011, 86:923-927. [3]Mahajan G, Sharma S, Chandra J, et al. Hepcidin and iron parameters in children with anemia of chronic disease and iron deficiency anemia[J]. Blood Res, 2017, 52:212-217. [4]Skikne BS. Serum transferrin receptor[J]. Am J Hematol, 2008, 83:872-875. [5]Infusino I, Braga F, Dolci A, et al. Soluble transferrin receptor (sTfR) and sTfR/log ferritin Index for the diagnosis of iron-deficiency anemia a meta-analysis[J]. Am J Clin Pathol, 2012, 138:642-649. [6]Rehu M, Ahonen S, Punnonen K. The diagnostic accuracy of the percentage of hypochromic red blood cells (%HYPOm) and cellular hemoglobin in reticulocytes (CHr) in differentiating iron deficiency anemia and anemia of chronic diseases[J]. Clin Chim Acta, 2011, 412:1809-1813. [7]Vicinanza P, Vicinanza M, Cosimato V. Mean reticol-ocyte hemoglobin content index plays a key role to identify children who are carriers of β-thalassemia[J]. Transl Med UniSa, 2018, 17:34-39. [8]Ceylan C, Miskioğlu M, Colak H, et al. Evaluation of reticulocyte parameters in iron deficiency, vitamin B12 deficiency and β-thalassemia minor patients[J]. Int J Lab Hematol, 2007, 29:327-334. [9]Khatami S, Dehnabeh SR, Mostafavi E, et al. Evaluation and comparison of soluble transferrin receptor in thalassemia carriers and iron deficient patients[J]. Hemoglobin, 2013, 37:387-395. [10]Baillie FJ, Morrison AE, Fergus I. Soluble transferrin receptor: a discriminating assay for iron deficiency[J]. Clin Lab Hematol, 2003, 25:353-357. [11]Pasricha SR, Frazer DM, Bowden DK, et al. Transfusion suppresses erythropoiesis and increases hepcidin in adult patients with β-thalassemia major: a longitudinal study[J]. Blood, 2013, 122:124-133. [12]Wang CY, Babitt JL. Hepcidin regulation in the anemia of inflammation[J]. Curr Opin Hematol, 2016, 23:189-197. |