Beta-talassæmi intermedia og minor
Farmakologisk induktion af føtal hæmoglobinsyntese
Behandling med hydroxyurea (hydroxycarbamid)
Optimizing the dose of hydroxyurea therapy for patients with β-thalassemia intermedia (Hb E-β-thalassemia): a single center study from eastern India. (åbner nyt vindue)
Kilde: Hemoglobin 2014;38(1):44-8.
Indekseret: PubMed 24144212
DOI: 10.3109/03630269.2013.845844
https://www.ncbi.nlm.nih.gov/pubmed/24144212 (åbner nyt vindue)
Hydroxyurea in thalassemia intermedia--a promising therapy. (åbner nyt vindue)
Kilde: Ann Hematol 2005;84(7):441-6.
Indekseret: PubMed 15838670
DOI: 10.1007/s00277-005-1026-4
https://www.ncbi.nlm.nih.gov/pubmed/15838670 (åbner nyt vindue)
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. (åbner nyt vindue)
Kilde: J Clin Pathol 2010;63(2):147-50.
Indekseret: PubMed 20154037
DOI: 10.1136/jcp.2009.070391
https://www.ncbi.nlm.nih.gov/pubmed/20154037 (åbner nyt vindue)
Echocardiographic finding in beta-thalassemia intermedia and major: absence of pulmonary hypertension following hydroxyurea treatment in beta-thalassemia intermedia. (åbner nyt vindue)
Kilde: Eur J Haematol 2009;82(3):213-8.
Indekseret: PubMed 19077048
DOI: 10.1111/j.1600-0609.2008.01192.x
https://www.ncbi.nlm.nih.gov/pubmed/19077048 (åbner nyt vindue)
Effect of combination therapy of hydroxyurea with l-carnitine and magnesium chloride on hematologic parameters and cardiac function of patients with beta-thalassemia intermedia. (åbner nyt vindue)
Kilde: Eur J Haematol 2010;84(1):52-8.
Indekseret: PubMed 19799627
DOI: 10.1111/j.1600-0609.2009.01356.x
https://www.ncbi.nlm.nih.gov/pubmed/19799627 (åbner nyt vindue)
Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece. (åbner nyt vindue)
Kilde: Blood Cells Mol Dis 2000;26(5):453-66.
Indekseret: PubMed 11112383
DOI: 10.1006/bcmd.2000.0328
https://www.ncbi.nlm.nih.gov/pubmed/11112383 (åbner nyt vindue)
Fetal globin stimulant therapies in the beta-hemoglobinopathies: principles and current potential. (åbner nyt vindue)
Kilde: Pediatr Ann 2008;37(5):339-46.
Indekseret: PubMed 18543545
https://www.ncbi.nlm.nih.gov/pubmed/18543545 (åbner nyt vindue)
Single and combination drug therapy for fetal hemoglobin augmentation in hemoglobin E-beta 0-thalassemia: Considerations for treatment. (åbner nyt vindue)
Kilde: Ann N Y Acad Sci 2005;1054:250-6.
Indekseret: PubMed 16339672
DOI: 10.1196/annals.1345.031
https://www.ncbi.nlm.nih.gov/pubmed/16339672 (åbner nyt vindue)
Rekombinant erytropoietin (alene eller kombineret med andre lægemidler)
Treatment of beta-thalassemia patients with recombinant human erythropoietin: effect on transfusion requirements and soluble adhesion molecules. (åbner nyt vindue)
Kilde: Acta Haematol 2004;111(4):189-95.
Indekseret: PubMed 15153710
DOI: 10.1159/000077551
https://www.ncbi.nlm.nih.gov/pubmed/15153710 (åbner nyt vindue)
Efficacy of erythropoietin on dialysis in patients with beta thalassemia minor. (åbner nyt vindue)
Kilde: Blood Purif 2004;22(5):453-60.
Indekseret: PubMed 15359104
DOI: 10.1159/000080729
https://www.ncbi.nlm.nih.gov/pubmed/15359104 (åbner nyt vindue)
The role of recombinant human erythropoietin in the treatment of thalassemia. (åbner nyt vindue)
Kilde: Ann N Y Acad Sci 1998;850:129-38.
Indekseret: PubMed 9668535
https://www.ncbi.nlm.nih.gov/pubmed/9668535 (åbner nyt vindue)
Darbepoetin alfa for the treatment of anaemia in alpha- or beta- thalassaemia intermedia syndromes. (åbner nyt vindue)
Kilde: Br J Haematol 2011;154(2):281-4.
Indekseret: PubMed 21496003
DOI: 10.1111/j.1365-2141.2011.08617.x
https://www.ncbi.nlm.nih.gov/pubmed/21496003 (åbner nyt vindue)
The emerging role of fetal hemoglobin induction in non-transfusion-dependent thalassemia. (åbner nyt vindue)
Kilde: Blood Rev 2012;26 Suppl 1:S35-9.
Indekseret: PubMed 22631042
DOI: 10.1016/S0268-960X(12)70011-5
https://www.ncbi.nlm.nih.gov/pubmed/22631042 (åbner nyt vindue)