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Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (otvara novi prozor)

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. (otvara novi prozor)

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. (otvara novi prozor)

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. (otvara novi prozor)

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Izvor‎: 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. (otvara novi prozor)

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Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (otvara novi prozor)

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Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients. (otvara novi prozor)

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. (otvara novi prozor)

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

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

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Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (otvara novi prozor)

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

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

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The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (otvara novi prozor)

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Izvor‎: 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. (otvara novi prozor)

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

Indeks‎: PubMed 18955291

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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. (otvara novi prozor)

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

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

Indeks‎: PubMed 23530969

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Butyric acid: what is the future for this old substance? (otvara novi prozor)

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Izvor‎: Swiss Med Wkly 2012;142:w13596.

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