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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]
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] Page: [Next] [New Search]