Optimizing the dose of hydroxyurea therapy for patients with β-thalassemia intermedia (Hb E-β-thalassemia): a single center study from eastern India. (mở cửa sổ mới)

Bohara VV, Ray S, Chakrabarti P, Ray SS, Nath UK, Chaudhuri U.

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 (mở cửa sổ mới)

Hydroxyurea in thalassemia intermedia--a promising therapy. (mở cửa sổ mới)

Dixit A, Chatterjee TC, Mishra P, Choudhry DR, Mahapatra M, Tyagi S, Kabra M, Saxena R, Choudhry VP.

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 (mở cửa sổ mới)

Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. (mở cửa sổ mới)

Italia KY, Jijina FF, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB.

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 (mở cửa sổ mới)

Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (mở cửa sổ mới)

Karimi M, Borzouee M, Mehrabani A, Cohan N.

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 (mở cửa sổ mới)

Effect of combination therapy of hydroxyurea with l-carnitine and magnesium chloride on hematologic parameters and cardiac function of patients with beta-thalassemia intermedia. (mở cửa sổ mới)

Karimi M, Mohammadi F, Behmanesh F, Samani SM, Borzouee M, Amoozgar H, Haghpanah S.

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 (mở cửa sổ mới)

Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece. (mở cửa sổ mới)

Loukopoulos D, Voskaridou E, Kalotychou V, Schina M, Loutradi A, Theodoropoulos I.

Nguồn‎: Blood Cells Mol Dis 2000;26(5):453-66.

Mã bài‎: PubMed 11112383

DOI‎: 10.1006/bcmd.2000.0328

https://www.ncbi.nlm.nih.gov/pubmed/11112383 (mở cửa sổ mới)

Fetal globin stimulant therapies in the beta-hemoglobinopathies: principles and current potential. (mở cửa sổ mới)

Perrine SP.

Nguồn‎: Pediatr Ann 2008;37(5):339-46.

Mã bài‎: PubMed 18543545

https://www.ncbi.nlm.nih.gov/pubmed/18543545 (mở cửa sổ mới)

Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatment. (mở cửa sổ mới)

Singer ST, Kuypers FA, Olivieri NF, Weatherall DJ, Mignacca R, Coates TD, Davies S, Sweeters N, Vichinsky EP.

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 (mở cửa sổ mới)

Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (mở cửa sổ mới)

Chaidos A, Makis A, Hatzimichael E, Tsiara S, Gouva M, Tzouvara E, Bourantas KL.

Nguồn‎: Acta Haematol 2004;111(4):189-95.

Mã bài‎: PubMed 15153710

DOI‎: 10.1159/000077551

https://www.ncbi.nlm.nih.gov/pubmed/15153710 (mở cửa sổ mới)

Efficacy of erythropoietin on dialysis in patients with beta thalassemia minor. (mở cửa sổ mới)

Di Iorio B, De Nicola L, Bellizzi V, Minutolo R, Zamboli P, Rubino R, Fuiano G, Conte G.

Nguồn‎: Blood Purif 2004;22(5):453-60.

Mã bài‎: PubMed 15359104

DOI‎: 10.1159/000080729

https://www.ncbi.nlm.nih.gov/pubmed/15359104 (mở cửa sổ mới)

The role of recombinant human erythropoietin in the treatment of thalassemia. (mở cửa sổ mới)

Rachmilewitz EA, Aker M.

Nguồn‎: Ann N Y Acad Sci 1998;850:129-38.

Mã bài‎: PubMed 9668535

https://www.ncbi.nlm.nih.gov/pubmed/9668535 (mở cửa sổ mới)

Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (mở cửa sổ mới)

Singer ST, Vichinsky EP, Sweeters N, Rachmilewitz E.

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 (mở cửa sổ mới)

The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (mở cửa sổ mới)

Thein SL.

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 (mở cửa sổ mới)