Efficacy of hydroxyurea in providing transfusion independence in β-thalassemia. (opens new window)

Ansari SH, Shamsi TS, Ashraf M, Perveen K, Farzana T, Bohray M, Erum S, Mehboob T.

Avots‎: J Pediatr Hematol Oncol 2011;33(5):339-43.

Raksts indeksēts‎: PubMed 21602718

DOI‎: 10.1097/MPH.0b013e31821b0770

https://www.ncbi.nlm.nih.gov/pubmed/21602718 (opens new window)

Gγ-Xmn I polymorphism: a significant determinant of β-thalassemia treatment without blood transfusion. (opens new window)

Ansari SH, Shamsi TS, Munzir S, Khan MT, Erum S, Perveen K, Farzana T, Ashraf M, Mehboob T, Moinuddin M.

Avots‎: J Pediatr Hematol Oncol 2013;35(4):e153-6.

Raksts indeksēts‎: PubMed 23389500

DOI‎: 10.1097/MPH.0b013e31827e8662

https://www.ncbi.nlm.nih.gov/pubmed/23389500 (opens new window)

Efficacy of hydroxyurea (HU) in reduction of pack red cell (PRC) transfusion requirement among children having beta-thalassemia major: Karachi HU trial (KHUT). (opens new window)

Ansari SH, Shamsi TS, Siddiqui FJ, Irfan M, Perveen K, Farzana T, Panjwani VK, Yousuf A, Mehboob T.

Avots‎: J Pediatr Hematol Oncol 2007;29(11):743-6.

Raksts indeksēts‎: PubMed 17984691

DOI‎: 10.1097/MPH.0b013e318157fd75

https://www.ncbi.nlm.nih.gov/pubmed/17984691 (opens new window)

Hydroxyurea can eliminate transfusion requirements in children with severe beta-thalassemia. (opens new window)

Bradai M, Abad MT, Pissard S, Lamraoui F, Skopinski L, de Montalembert M.

Avots‎: Blood 2003;102(4):1529-30.

Raksts indeksēts‎: PubMed 12702505

DOI‎: 10.1182/blood-2003-01-0117

https://www.ncbi.nlm.nih.gov/pubmed/12702505 (opens new window)

Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia. (opens new window)

Bradai M, Pissard S, Abad MT, Dechartres A, Ribeil JA, Landais P, de Montalembert M.

Avots‎: Transfusion 2007;47(10):1830-6.

Raksts indeksēts‎: PubMed 17880608

DOI‎: 10.1111/j.1537-2995.2007.01399.x

https://www.ncbi.nlm.nih.gov/pubmed/17880608 (opens new window)

Hydroxyurea can reduce or eliminate transfusion requirements in children with major and intermediate thalassemia. (opens new window)

Hashemi A, Abrishamkar M, Jenabzade AR, Eslami Z.

Avots‎: Iran J Blood Cancer 2009;1(4):147-50.

Raksts indeksēts‎: IMEMR 107228

https://www.ijbc.ir/browse.php?a_id=4&sid=1&slc_lang=en (opens new window)

Genotype-phenotype relationship of patients with β-thalassemia taking hydroxyurea: a 13-year experience in Iran. (opens new window)

Karimi M, Haghpanah S, Farhadi A, Yavarian M.

Avots‎: Int J Hematol 2012;95(1):51-6.

Raksts indeksēts‎: PubMed 22180324

DOI‎: 10.1007/s12185-011-0985-6

https://www.ncbi.nlm.nih.gov/pubmed/22180324 (opens new window)

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

https://www.ncbi.nlm.nih.gov/pubmed/18543545 (opens new window)

A randomised double-blind placebo-controlled clinical trial of oral hydroxyurea for transfusion-dependent β-thalassaemia. (opens new window)

Yasara N, Wickramarathne N, Mettananda C, Silva I, Hameed N, Attanayaka K, Rodrigo R, Wickramasinghe N, Perera L, Manamperi A, Premawardhena A, Mettananda S

Avots‎: Sci Rep. 2022;12(1):2752.

Raksts indeksēts‎: PubMed 35177777

DOI‎: 10.1038/s41598-022-06774-8

https://pubmed.ncbi.nlm.nih.gov/35177777/ (opens new window)

Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients. (opens new window)

Yavarian M, Karimi M, Bakker E, Harteveld CL, Giordano PC.

Avots‎: Haematologica 2004;89(10):1172-8.

Raksts indeksēts‎: PubMed 15477200

https://www.ncbi.nlm.nih.gov/pubmed/15477200 (opens new window)

Hydroxyurea therapy in 49 patients with major beta-thalassemia. (opens new window)

Zamani F, Shakeri R, Eslami SM, Razavi SM, Basi A.

Avots‎: Arch Iran Med 2009;12(3):295-7.

Raksts indeksēts‎: PubMed 19400608

https://www.ncbi.nlm.nih.gov/pubmed/19400608 (opens new window)

Use of hydroxyurea and recombinant erythropoietin in management of homozygous ß⁰ thalassemia. (opens new window)

Kohli-Kumar M, Marandi H, Keller MA, Guertin K, Hvizdala E.

Avots‎: J Pediatr Hematol Oncol 2002;24(9):777-8.

Raksts indeksēts‎: PubMed 12468925

https://www.ncbi.nlm.nih.gov/pubmed/12468925 (opens new window)

Termination of transfusion dependence in beta-thalassemia: two-year experience with recombinant human erythropoietin. (opens new window)

Nişli G, Kavakli K, Aydinok Y, Oztop S, Cetingül N.

Avots‎: Pediatr Hematol Oncol 1997;14(3):285-7.

Raksts indeksēts‎: PubMed 9185215

https://www.ncbi.nlm.nih.gov/pubmed/9185215 (opens new window)

Fetal globin gene inducers: novel agents and new potential. (opens new window)

Perrine SP, Castaneda SA, Chui DH, Faller DV, Berenson RJ, Siritanaratku N, Fucharoen S.

Avots‎: Ann N Y Acad Sci 2010;1202:158-64.

Raksts indeksēts‎: PubMed 20712788

DOI‎: 10.1111/j.1749-6632.2010.05593.x

https://www.ncbi.nlm.nih.gov/pubmed/20712788 (opens new window)