重型β地中海貧血
藥物誘導胎兒血紅蛋白合成
羥基脲治療
Efficacy of hydroxyurea in providing transfusion independence in β-thalassemia. (開啟新視窗)
來源: J Pediatr Hematol Oncol 2011;33(5):339-43.
檢索: PubMed 21602718
DOI碼: 10.1097/MPH.0b013e31821b0770
Hydroxyurea treatment in β-thalassemia patients: to respond or not to respond? (開啟新視窗)
來源: Ann Hematol 2013;92(3):289-99.
檢索: PubMed 23318979
DOI碼: 10.1007/s00277-012-1671-3
Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia. (開啟新視窗)
來源: Transfusion 2007;47(10):1830-6.
檢索: PubMed 17880608
DOI碼: 10.1111/j.1537-2995.2007.01399.x
Hydroxyurea increases hemoglobin F levels and improves the effectiveness of erythropoiesis in beta-thalassemia/hemoglobin E disease. (開啟新視窗)
來源: Blood 1996;87(3):887-92.
檢索: PubMed 8562958
Hydroxyurea can reduce or eliminate transfusion requirements in children with major and intermediate thalassemia. (開啟新視窗)
來源: Iran J Blood Cancer 2009;1(4):147-50.
檢索: IMEMR 107228
https://www.ijbc.ir/browse.php?a_id=4&sid=1&slc_lang=en (開啟新視窗)
Hydroxyurea as a first-line treatment of extramedullary hematopoiesis in patients with beta thalassemia: Four case reports. (開啟新視窗)
來源: Hematology 2015;20(1):53-7.
檢索: PubMed 24717020
DOI碼: 10.1179/1607845414Y.0000000168
Genotype-phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran. (開啟新視窗)
來源: Int J Hematol 2012;95(1):51-6.
檢索: PubMed 22180324
DOI碼: 10.1007/s12185-011-0985-6
Report on Patients with Non Transfusion-Dependent β-Thalassemia Major Being Treated with Hydroxyurea Attending the Thalassemia Research Center, Sari, Mazandaran Province, Islamic Republic of Iran in 2013. (開啟新視窗)
來源: Hemoglobin 2014;38(2):115-8.
檢索: PubMed 24471558
DOI碼: 10.3109/03630269.2013.869229
Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia. (開啟新視窗)
來源: Blood 2013;121(12):2199-212.
檢索: PubMed 23315167
DOI碼: 10.1182/blood-2012-10-408021
A randomised double-blind placebo-controlled clinical trial of oral hydroxyurea for transfusion-dependent β-thalassaemia. (開啟新視窗)
來源: Sci Rep. 2022;12(1):2752.
檢索: PubMed 35177777
DOI碼: 10.1038/s41598-022-06774-8
Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients. (開啟新視窗)
來源: Haematologica 2004;89(10):1172-8.
檢索: PubMed 15477200
Hydroxyurea therapy in 49 patients with major beta-thalassemia. (開啟新視窗)
來源: Arch Iran Med 2009;12(3):295-7.
檢索: PubMed 19400608
重組人促紅細胞生成素(單用或跟其他藥物聯合使用)
Preliminary results with administration of recombinant human erythropoietin in sickle cell/beta-thalassemia patients during pregnancy. (開啟新視窗)
來源: Eur J Haematol 1996;56(5):326-8.
檢索: PubMed 8641410
Induction of fetal hemoglobin synthesis with recombinant human erythropoietin in anemic patients with heterozygous beta-thalassemia during pregnancy. (開啟新視窗)
來源: J Matern Fetal Med 1999;8(1):1-7.
檢索: PubMed 10052837
DOI碼: 10.1002/(SICI)1520-6661(199901/02)8:1<1::AID-MFM1>3.0.CO;2-O
Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (開啟新視窗)
來源: Acta Haematol 2004;111(4):189-95.
檢索: PubMed 15153710
DOI碼: 10.1159/000077551
Recombinant human erythropoietin therapy in a transfusion-dependent β-thalassemia major patient. (開啟新視窗)
來源: Ann Hematol 2001;80(8):492-5.
檢索: PubMed 11563599
Fetal globin induction--can it cure beta thalassemia? (開啟新視窗)
來源: Hematology Am Soc Hematol Educ Program 2005:38-44.
檢索: PubMed 16304357
DOI碼: 10.1182/asheducation-2005.1.38