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Journal Abstract Search


1052 related items for PubMed ID: 19545554

  • 1. Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.
    Italia KY, Jijina FJ, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB.
    Clin Chim Acta; 2009 Sep; 407(1-2):10-5. PubMed ID: 19545554
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  • 2. Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype.
    Italia K, Jain D, Gattani S, Jijina F, Nadkarni A, Sawant P, Nair S, Mohanty D, Ghosh K, Colah R.
    Blood Cells Mol Dis; 2009 Sep; 42(1):25-31. PubMed ID: 18954999
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  • 3. Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study.
    Italia KY, Jijina FF, Merchant R, Panjwani S, Nadkarni AH, Sawant PM, Nair SB, Ghosh K, Colah RB.
    J Clin Pathol; 2010 Feb; 63(2):147-50. PubMed ID: 20154037
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  • 4. Hydroxyurea-induced hematological response in transfusion-independent beta-thalassemia intermedia: case series and review of literature.
    Ehsani MA, Hedayati-Asl AA, Bagheri A, Zeinali S, Rashidi A.
    Pediatr Hematol Oncol; 2009 Nov; 26(8):560-5. PubMed ID: 19954365
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  • 5. Response to hydroxyurea therapy in beta-thalassemia.
    Koren A, Levin C, Dgany O, Kransnov T, Elhasid R, Zalman L, Palmor H, Tamary H.
    Am J Hematol; 2008 May; 83(5):366-70. PubMed ID: 18181203
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  • 6. Response to hydroxyurea treatment in Iranian transfusion-dependent beta-thalassemia patients.
    Yavarian M, Karimi M, Bakker E, Harteveld CL, Giordano PC.
    Haematologica; 2004 Oct; 89(10):1172-8. PubMed ID: 15477200
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  • 7. Hydroxyurea in thalassemia intermedia--a promising therapy.
    Dixit A, Chatterjee TC, Mishra P, Choudhry DR, Mahapatra M, Tyagi S, Kabra M, Saxena R, Choudhry VP.
    Ann Hematol; 2005 Jul; 84(7):441-6. PubMed ID: 15838670
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  • 8. Decreased transfusion needs associated with hydroxyurea therapy in Algerian patients with thalassemia major or intermedia.
    Bradai M, Pissard S, Abad MT, Dechartres A, Ribeil JA, Landais P, de Montalembert M.
    Transfusion; 2007 Oct; 47(10):1830-6. PubMed ID: 17880608
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  • 9. Hydroxyurea in the treatment of major beta-thalassemia and importance of genetic screening.
    Alebouyeh M, Moussavi F, Haddad-Deylami H, Vossough P.
    Ann Hematol; 2004 Jul; 83(7):430-3. PubMed ID: 14722738
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  • 14. Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece.
    Loukopoulos D, Voskaridou E, Kalotychou V, Schina M, Loutradi A, Theodoropoulos I.
    Blood Cells Mol Dis; 2000 Oct; 26(5):453-66. PubMed ID: 11112383
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  • 16. Nucleotide -88 (C-T) promoter mutation is a common beta-thalassemia mutation in the Jat Sikhs of Punjab, India.
    Garewal G, Das R, Ahluwalia J, Marwaha RK, Varma S.
    Am J Hematol; 2005 Aug; 79(4):252-6. PubMed ID: 16044458
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  • 17. Asymptomatic and mild beta-thalassemia in homozygotes and compound heterozygotes for the IVS2+1G-->A mutation: role of the beta-globin gene haplotype.
    Ragusa A, Amata S, Lombardo T, Castiglia L, Maier-Redelsperger M, Labie D, Bernini L.
    Haematologica; 2003 Oct; 88(10):1099-105. PubMed ID: 14555304
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  • 20. Do alpha deletions influence hydroxyurea response in thalassemia intermedia?
    Panigrahi I, Dixit A, Arora S, Kabra M, Mahapatra M, Choudhry VP, Saxena R.
    Hematology; 2005 Feb; 10(1):61-3. PubMed ID: 16019448
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