Bệnh thiếu máu huyết tán Beta thể trung gian và thể nhẹ (ở trẻ em)
Bệnh thiếu máu huyết tán Beta thể trung gian và thể nhẹ—Thuốc sản sinh hemoglobin thai nhi
Liệu pháp Hydroxyurea (Hydroxycarbamide)
Optimizing the dose of hydroxyurea therapy for patients with β-thalassemia intermedia (Hb E-β-thalassemia): a single center study from eastern India. (opens new window)
Nguồn: Hemoglobin 2014;38(1):44-8.
Mã bài: PubMed 24144212
DOI: 10.3109/03630269.2013.845844
https://www.ncbi.nlm.nih.gov/pubmed/24144212 (opens new window)
Hydroxyurea in thalassemia intermedia--a promising therapy. (opens new window)
Nguồn: Ann Hematol 2005;84(7):441-6.
Mã bài: PubMed 15838670
DOI: 10.1007/s00277-005-1026-4
https://www.ncbi.nlm.nih.gov/pubmed/15838670 (opens new window)
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. (opens new window)
Nguồn: J Clin Pathol 2010;63(2):147-50.
Mã bài: PubMed 20154037
DOI: 10.1136/jcp.2009.070391
https://www.ncbi.nlm.nih.gov/pubmed/20154037 (opens new window)
Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (opens new window)
Nguồn: Eur J Haematol 2009;82(3):213-8.
Mã bài: PubMed 19077048
DOI: 10.1111/j.1600-0609.2008.01192.x
https://www.ncbi.nlm.nih.gov/pubmed/19077048 (opens new window)
Hematologic and clinical responses of thalassemia intermedia patients to hydroxyurea during 6 years of therapy in Iran. (opens new window)
Nguồn: J Pediatr Hematol Oncol 2005;27(7):380-5.
Mã bài: PubMed 16012328
https://www.ncbi.nlm.nih.gov/pubmed/16012328 (opens new window)
Effect of combination therapy of hydroxyurea with l-carnitine and magnesium chloride on hematologic parameters and cardiac function of patients with beta-thalassemia intermedia. (opens new window)
Nguồn: Eur J Haematol 2010;84(1):52-8.
Mã bài: PubMed 19799627
DOI: 10.1111/j.1600-0609.2009.01356.x
https://www.ncbi.nlm.nih.gov/pubmed/19799627 (opens new window)
The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: a preliminary study. (opens new window)
Nguồn: Pediatr Hematol Oncol 2003;20(6):429-34.
Mã bài: PubMed 14631615
https://www.ncbi.nlm.nih.gov/pubmed/14631615 (opens new window)
Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatment. (opens new window)
Nguồn: Ann N Y Acad Sci 2005;1054:250-6.
Mã bài: PubMed 16339672
DOI: 10.1196/annals.1345.031
https://www.ncbi.nlm.nih.gov/pubmed/16339672 (opens new window)
Erythropoietin tái tổ hợp (dùng riêng hoặc kết hợp với các thuốc khác)
Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (opens new window)
Nguồn: Acta Haematol 2004;111(4):189-95.
Mã bài: PubMed 15153710
DOI: 10.1159/000077551
https://www.ncbi.nlm.nih.gov/pubmed/15153710 (opens new window)
Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients. (opens new window)
Nguồn: Eur J Haematol 2013;91(6):522-33.
Mã bài: PubMed 23927461
DOI: 10.1111/ejh.12182
https://www.ncbi.nlm.nih.gov/pubmed/23927461 (opens new window)
Fetal globin stimulant therapies in the beta-hemoglobinopathies: principles and current potential. (opens new window)
Nguồn: Pediatr Ann 2008;37(5):339-46.
Mã bài: PubMed 18543545
https://www.ncbi.nlm.nih.gov/pubmed/18543545 (opens new window)
Sustained increase in haemoglobin and RBC following long-term administration of recombinant human erythropoietin to patients with homozygous beta-thalassaemia. (opens new window)
Nguồn: Br J Haematol 1995;90(2):341-5.
Mã bài: PubMed 7794754
https://www.ncbi.nlm.nih.gov/pubmed/7794754 (opens new window)
Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (opens new window)
Nguồn: Br J Haematol 2011;154(2):281-4.
Mã bài: PubMed 21496003
DOI: 10.1111/j.1365-2141.2011.08617.x
https://www.ncbi.nlm.nih.gov/pubmed/21496003 (opens new window)
The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (opens new window)
Nguồn: Blood Rev 2012;26 Suppl 1:S35-9.
Mã bài: PubMed 22631042
DOI: 10.1016/S0268-960X(12)70011-5
https://www.ncbi.nlm.nih.gov/pubmed/22631042 (opens new window)
Các thuốc khác
Fetal hemoglobin inducers from the natural world: a novel approach for identification of drugs for the treatment of {beta}-thalassemia and sickle-cell anemia. (opens new window)
Nguồn: Evid Based Complement Alternat Med 2009;6(2):141-51.
Mã bài: PubMed 18955291
DOI: 10.1093/ecam/nem139
https://www.ncbi.nlm.nih.gov/pubmed/18955291 (opens new window)
A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia. (opens new window)
Nguồn: Br J Haematol 2013;161(4):587-93.
Mã bài: PubMed 23530969
DOI: 10.1111/bjh.12304
https://www.ncbi.nlm.nih.gov/pubmed/23530969 (opens new window)
Butyric acid: what is the future for this old substance? (opens new window)
Nguồn: Swiss Med Wkly 2012;142:w13596.
Mã bài: PubMed 22674349
DOI: 10.4414/smw.2012.13596
https://www.ncbi.nlm.nih.gov/pubmed/22674349 (opens new window)