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Journal Abstract Search


125 related items for PubMed ID: 25811748

  • 1. Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt.
    Adly AA, Ebeid FS.
    J Pediatr Hematol Oncol; 2015 May; 37(4):281-4. PubMed ID: 25811748
    [Abstract] [Full Text] [Related]

  • 2. Major risk of blood transfusion in hemolytic anemia patients.
    Omar N, Salama K, Adolf S, El-Saeed GS, Abdel Ghaffar N, Ezzat N.
    Blood Coagul Fibrinolysis; 2011 Jun; 22(4):280-4. PubMed ID: 21508832
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Prevalence of HBV and HCV infection among multi-transfused Egyptian thalassemic patients.
    Mansour AK, Aly RM, Abdelrazek SY, Elghannam DM, Abdelaziz SM, Shahine DA, Elmenshawy NM, Darwish AM.
    Hematol Oncol Stem Cell Ther; 2012 Jun; 5(1):54-9. PubMed ID: 22446611
    [Abstract] [Full Text] [Related]

  • 5. Prevalence of hepatitis C infection among children with β-thalassaemia major in Mid Delta, Egypt: a single centre study.
    El-Shanshory MR, Kabbash IA, Soliman HH, Nagy HM, Abdou SH.
    Trans R Soc Trop Med Hyg; 2013 Apr; 107(4):224-8. PubMed ID: 23343507
    [Abstract] [Full Text] [Related]

  • 6. Consequences and costs of noncompliance with iron chelation therapy in patients with transfusion-dependent thalassemia: a literature review.
    Delea TE, Edelsberg J, Sofrygin O, Thomas SK, Baladi JF, Phatak PD, Coates TD.
    Transfusion; 2007 Oct; 47(10):1919-29. PubMed ID: 17880620
    [Abstract] [Full Text] [Related]

  • 7. Outcomes, utilization, and costs among thalassemia and sickle cell disease patients receiving deferoxamine therapy in the United States.
    Delea TE, Hagiwara M, Thomas SK, Baladi JF, Phatak PD, Coates TD.
    Am J Hematol; 2008 Apr; 83(4):263-70. PubMed ID: 17924547
    [Abstract] [Full Text] [Related]

  • 8. Thalassemia treatment and prevention in Uva Province, Sri Lanka: a public opinion survey.
    Mudiyanse RM.
    Hemoglobin; 2006 Apr; 30(2):275-89. PubMed ID: 16798653
    [Abstract] [Full Text] [Related]

  • 9. Abnormal glucose tolerance in Egyptian beta-thalassemic patients: possible association with genotyping.
    Khalifa AS, Salem M, Mounir E, El-Tawil MM, El-Sawy M, Abd Al-Aziz MM.
    Pediatr Diabetes; 2004 Sep; 5(3):126-32. PubMed ID: 15450007
    [Abstract] [Full Text] [Related]

  • 10. Combined therapy with desferrioxamine and deferiprone in beta thalassemia major patients with transfusional iron overload.
    Daar S, Pathare AV.
    Ann Hematol; 2006 May; 85(5):315-9. PubMed ID: 16450126
    [Abstract] [Full Text] [Related]

  • 11. Prolonged survival in patients with beta-thalassemia major treated with deferoxamine.
    Ehlers KH, Giardina PJ, Lesser ML, Engle MA, Hilgartner MW.
    J Pediatr; 1991 Apr; 118(4 Pt 1):540-5. PubMed ID: 2007928
    [Abstract] [Full Text] [Related]

  • 12. Combined chelation therapy with deferoxamine and deferiprone in β-thalassemia major: compliance and opinions of young thalassemic patients.
    Hatzipantelis ES, Karasmanis K, Perifanis V, Vlachaki E, Tziomalos K, Economou M.
    Hemoglobin; 2014 Apr; 38(2):111-4. PubMed ID: 24351163
    [Abstract] [Full Text] [Related]

  • 13. Antibody titration and immune response of Iranian beta-thalassemic patients to hepatitis B virus vaccine (booster effect).
    Azarkeivan A, Karimi G, Shaiegan M, Maghsudlu M, Tabbaroki A.
    Pediatr Hematol Oncol; 2009 Jun; 26(4):195-201. PubMed ID: 19437322
    [Abstract] [Full Text] [Related]

  • 14. Red cell alloimmunization and infectious marker status (human immunodeficiency virus, hepatitis B virus and hepatitis C virus) in multiply transfused thalassemia patients of North India.
    Makroo RN, Arora JS, Chowdhry M, Bhatia A, Thakur UK, Minimol A.
    Indian J Pathol Microbiol; 2013 Jun; 56(4):378-83. PubMed ID: 24441225
    [Abstract] [Full Text] [Related]

  • 15. Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapy.
    Karakukcu C, Karakukcu M, Unal E, Patiroglu T, Ozdemir MA, Torun YA, Tang PH.
    Hemoglobin; 2012 Jun; 36(3):219-29. PubMed ID: 22483337
    [Abstract] [Full Text] [Related]

  • 16. Chelation therapy in beta-thalassemia major. III. The role of splenectomy in achieving iron balance.
    Graziano JH, Piomelli S, Hilgartner M, Giardina P, Karpatkin M, Andrew M, LoIacono N, Seaman C.
    J Pediatr; 1981 Nov; 99(5):695-9. PubMed ID: 7299540
    [Abstract] [Full Text] [Related]

  • 17. Quality of Life Outcomes in a Pediatric Thalassemia Population in Egypt.
    Adam S, Afifi H, Thomas M, Magdy P, El-Kamah G.
    Hemoglobin; 2017 Jan; 41(1):16-20. PubMed ID: 28440111
    [Abstract] [Full Text] [Related]

  • 18. [Chelating therapy in beta-thalassemia].
    Musumeci S, Romeo MA, Di Gregorio F, Schiliró G, Russo G.
    Pediatr Med Chir; 1982 Jan; 4(1-2):55-9. PubMed ID: 7111040
    [Abstract] [Full Text] [Related]

  • 19. Pilot study on the "quality of life" as reflected by psychosocial adjustment of children with thalassemia major undergoing iron-chelating treatment in western Taiwan.
    Kuo HT, Tsai MY, Peng CT, Wu KH.
    Hemoglobin; 2006 Jan; 30(2):291-9. PubMed ID: 16798654
    [Abstract] [Full Text] [Related]

  • 20. Chelation therapy and ferritin levels in patients with homozygous beta-thalassemia.
    Kattamis C, Lagos P, Langona E.
    Prog Clin Biol Res; 1979 Jan; 34():351-9. PubMed ID: 531060
    [No Abstract] [Full Text] [Related]


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