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Avots‎: Hemoglobin 2014;38(1):44-8.

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Hydroxyurea in thalassemia intermedia--a promising therapy. (opens new window)

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Avots‎: Ann Hematol 2005;84(7):441-6.

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Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. (opens new window)

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

Avots‎: J Clin Pathol 2010;63(2):147-50.

Raksts indeksēts‎: PubMed 20154037

DOI‎: 10.1136/jcp.2009.070391

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Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (opens new window)

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

Avots‎: Eur J Haematol 2009;82(3):213-8.

Raksts indeksēts‎: PubMed 19077048

DOI‎: 10.1111/j.1600-0609.2008.01192.x

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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)

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

Avots‎: Eur J Haematol 2010;84(1):52-8.

Raksts indeksēts‎: PubMed 19799627

DOI‎: 10.1111/j.1600-0609.2009.01356.x

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Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece. (opens new window)

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

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

Raksts indeksēts‎: PubMed 11112383

DOI‎: 10.1006/bcmd.2000.0328

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Fetal globin stimulant therapies in the beta-hemoglobinopathies: principles and current potential. (opens new window)

Perrine SP.

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

Raksts indeksēts‎: PubMed 18543545

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Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatment. (opens new window)

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

Avots‎: Ann N Y Acad Sci 2005;1054:250-6.

Raksts indeksēts‎: PubMed 16339672

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Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (opens new window)

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

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

Raksts indeksēts‎: PubMed 15153710

DOI‎: 10.1159/000077551

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Efficacy of erythropoietin on dialysis in patients with beta thalassemia minor. (opens new window)

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

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

Raksts indeksēts‎: PubMed 15359104

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The role of recombinant human erythropoietin in the treatment of thalassemia. (opens new window)

Rachmilewitz EA, Aker M.

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

Raksts indeksēts‎: PubMed 9668535

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Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (opens new window)

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

Avots‎: Br J Haematol 2011;154(2):281-4.

Raksts indeksēts‎: PubMed 21496003

DOI‎: 10.1111/j.1365-2141.2011.08617.x

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The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (opens new window)

Thein SL.

Avots‎: Blood Rev 2012;26 Suppl 1:S35-9.

Raksts indeksēts‎: PubMed 22631042

DOI‎: 10.1016/S0268-960X(12)70011-5

https://www.ncbi.nlm.nih.gov/pubmed/22631042 (opens new window)