These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
155 related items for PubMed ID: 20424435
1. Improved treatment satisfaction and convenience with deferasirox in iron-overloaded patients with beta-Thalassemia: Results from the ESCALATOR Trial. Taher A, Al Jefri A, Elalfy MS, Al Zir K, Daar S, Rofail D, Baladi JF, Habr D, Kriemler-Krahn U, El-Beshlawy A. Acta Haematol; 2010; 123(4):220-5. PubMed ID: 20424435 [Abstract] [Full Text] [Related]
2. Prospective evaluation of patient-reported outcomes during treatment with deferasirox or deferoxamine for iron overload in patients with beta-thalassemia. Cappellini MD, Bejaoui M, Agaoglu L, Porter J, Coates T, Jeng M, Lai ME, Mangiagli A, Strauss G, Girot R, Watman N, Ferster A, Loggetto S, Abish S, Cario H, Zoumbos N, Vichinsky E, Opitz H, Ressayre-Djaffer C, Abetz L, Rofail D, Baladi JF. Clin Ther; 2007 May; 29(5):909-917. PubMed ID: 17697909 [Abstract] [Full Text] [Related]
3. Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with beta-thalassaemia: the ESCALATOR study. Taher A, El-Beshlawy A, Elalfy MS, Al Zir K, Daar S, Habr D, Kriemler-Krahn U, Hmissi A, Al Jefri A. Eur J Haematol; 2009 Jun; 82(6):458-65. PubMed ID: 19187278 [Abstract] [Full Text] [Related]
4. Patient-reported outcomes of deferasirox (Exjade, ICL670) versus deferoxamine in sickle cell disease patients with transfusional hemosiderosis. Substudy of a randomized open-label phase II trial. Vichinsky E, Pakbaz Z, Onyekwere O, Porter J, Swerdlow P, Coates T, Lane P, Files B, Mueller BU, Coïc L, Forni GL, Fischer R, Marks P, Rofail D, Abetz L, Baladi JF. Acta Haematol; 2008 Jun; 119(3):133-41. PubMed ID: 18408362 [Abstract] [Full Text] [Related]
7. Efficacy and safety of a novel combination of two oral chelators deferasirox/deferiprone over deferoxamine/deferiprone in severely iron overloaded young beta thalassemia major patients. Elalfy MS, Adly AM, Wali Y, Tony S, Samir A, Elhenawy YI. Eur J Haematol; 2015 Nov; 95(5):411-20. PubMed ID: 25600572 [Abstract] [Full Text] [Related]
8. Efficacy and safety of deferasirox in β-thalassemia major patients in Iran: a prospective study from a single referral center in Iran. Alavi S, Ebadi M, Ghazizadeh F, Arzanian MT, Shamsian B, Abdollah Gorji F. Pediatr Hematol Oncol; 2014 Feb; 31(1):76-86. PubMed ID: 24383712 [Abstract] [Full Text] [Related]
10. Phase II clinical evaluation of deferasirox, a once-daily oral chelating agent, in pediatric patients with beta-thalassemia major. Galanello R, Piga A, Forni GL, Bertrand Y, Foschini ML, Bordone E, Leoni G, Lavagetto A, Zappu A, Longo F, Maseruka H, Hewson N, Sechaud R, Belleli R, Alberti D. Haematologica; 2006 Oct; 91(10):1343-51. PubMed ID: 17018383 [Abstract] [Full Text] [Related]
11. Reduction in labile plasma iron during treatment with deferasirox, a once-daily oral iron chelator, in heavily iron-overloaded patients with beta-thalassaemia. Daar S, Pathare A, Nick H, Kriemler-Krahn U, Hmissi A, Habr D, Taher A. Eur J Haematol; 2009 Jun; 82(6):454-7. PubMed ID: 19191863 [Abstract] [Full Text] [Related]
12. Daily alternating deferasirox and deferiprone therapy for "hard-to-chelate" beta-thalassemia major patients. Balocco M, Carrara P, Pinto V, Forni GL. Am J Hematol; 2010 Jun; 85(6):460-1. PubMed ID: 20513129 [No Abstract] [Full Text] [Related]
14. Results from a 1-year, open-label, single arm, multi-center trial evaluating the efficacy and safety of oral Deferasirox in patients diagnosed with low and int-1 risk myelodysplastic syndrome (MDS) and transfusion-dependent iron overload. Nolte F, Höchsmann B, Giagounidis A, Lübbert M, Platzbecker U, Haase D, Lück A, Gattermann N, Taupitz M, Baier M, Leismann O, Junkes A, Schumann C, Hofmann WK, Schrezenmeier H. Ann Hematol; 2013 Jan; 92(2):191-8. PubMed ID: 23073603 [Abstract] [Full Text] [Related]
15. Improvement in liver pathology of patients with β-thalassemia treated with deferasirox for at least 3 years. Deugnier Y, Turlin B, Ropert M, Cappellini MD, Porter JB, Giannone V, Zhang Y, Griffel L, Brissot P. Gastroenterology; 2011 Oct; 141(4):1202-11, 1211.e1-3. PubMed ID: 21741344 [Abstract] [Full Text] [Related]
17. Transitioning Patients With Iron Overload From Exjade to Jadenu. Tinsley SM, Hoehner-Cooper CM. J Infus Nurs; 2018 Oct; 41(3):171-175. PubMed ID: 29659464 [Abstract] [Full Text] [Related]
18. The effects of deferasirox on renal, cardiac and hepatic iron load in patients with β-thalassemia major: preliminary results. Unal S, Hazirolan T, Eldem G, Gumruk F. Pediatr Hematol Oncol; 2011 Apr; 28(3):217-21. PubMed ID: 21083355 [Abstract] [Full Text] [Related]
19. A prospective study of tubular dysfunction in pediatric patients with Beta thalassemia major receiving deferasirox. Naderi M, Sadeghi-Bojd S, Valeshabad AK, Jahantigh A, Alizadeh S, Dorgalaleh A, Tabibian S, Bamedi T. Pediatr Hematol Oncol; 2013 Nov; 30(8):748-54. PubMed ID: 24134694 [Abstract] [Full Text] [Related]
20. 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] Page: [Next] [New Search]