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Lähde‎: Hemoglobin 2014;38(1):44-8.

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Hydroxyurea in thalassemia intermedia--a promising therapy. (avaa uuden ikkunan)

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

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

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Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (avaa uuden ikkunan)

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

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Hematologic and clinical responses of thalassemia intermedia patients to hydroxyurea during 6 years of therapy in Iran. (avaa uuden ikkunan)

Karimi M, Darzi H, Yavarian M.

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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. (avaa uuden ikkunan)

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

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The effect of hydroxyurea on the coagulation system in sickle cell anemia and beta-thalassemia intermedia patients: a preliminary study. (avaa uuden ikkunan)

Koc A, Gumruk F, Gurgey A.

Lähde‎: Pediatr Hematol Oncol 2003;20(6):429-34.

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Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatment. (avaa uuden ikkunan)

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Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (avaa uuden ikkunan)

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Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients. (avaa uuden ikkunan)

Elalfy MS, Adly AA, Ismail EA, Elhenawy YI, Elghamry IR.

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Fetal globin stimulant therapies in the beta-hemoglobinopathies: principles and current potential. (avaa uuden ikkunan)

Perrine SP.

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Sustained increase in haemoglobin and RBC following long-term administration of recombinant human erythropoietin to patients with homozygous beta-thalassaemia. (avaa uuden ikkunan)

Rachmilewitz EA, Aker M, Perry D, Dover G.

Lähde‎: Br J Haematol 1995;90(2):341-5.

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Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (avaa uuden ikkunan)

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

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The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (avaa uuden ikkunan)

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

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Fetal hemoglobin inducers from the natural world: a novel approach for identification of drugs for the treatment of {beta}-thalassemia and sickle-cell anemia. (avaa uuden ikkunan)

Bianchi N, Zuccato C, Lampronti I, Borgatti M, Gambari R.

Lähde‎: Evid Based Complement Alternat Med 2009;6(2):141-51.

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A randomized phase I/II trial of HQK-1001, an oral fetal globin gene inducer, in β-thalassaemia intermedia and HbE/β-thalassaemia. (avaa uuden ikkunan)

Fucharoen S, Inati A, Siritanaratku N, Thein SL, Wargin WC, Koussa S, Taher A, Chaneim N, Boosalis M, Berenson R, Perrine SP.

Lähde‎: Br J Haematol 2013;161(4):587-93.

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Butyric acid: what is the future for this old substance? (avaa uuden ikkunan)

Sossai P.

Lähde‎: Swiss Med Wkly 2012;142:w13596.

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