Literature DB >> 10872476

Thalassaemia: clinical management.

N Olivieri1.   

Abstract

Advances in the management of thalassaemia major have greatly improved the prognosis for patients with this disease. In countries able to afford programmes of regular transfusion and iron-chelating therapy, survival to the fourth decade is now common, and most complications associated with the primary disease are now infrequently observed. This situation stands in contrast to that in emerging countries, where the widespread implementation of these expensive treatment regimens is still awaited. This review will focus on recent advances in the treatment of thalassaemia and briefly review the progress in experimental approaches to treatment of this disorder.

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Year:  1998        PMID: 10872476     DOI: 10.1016/s0950-3536(98)80073-5

Source DB:  PubMed          Journal:  Baillieres Clin Haematol        ISSN: 0950-3536


  3 in total

1.  The thalassemias and related disorders.

Authors:  Alain J Marengo-Rowe
Journal:  Proc (Bayl Univ Med Cent)       Date:  2007-01

2.  Red cell alloantibodies in beta-thalassaemia major patients' blood referring to the regional blood transfusion center of Tehran, Iran.

Authors:  Parisa Ebrahimisadr; Zahra Bakhshandeh; Hamidreza Majidiani
Journal:  Bioimpacts       Date:  2020-04-20

3.  A safety, pharmacokinetic and pharmacodynamic investigation of deferasirox (Exjade, ICL670) in patients with transfusion-dependent anemias and iron-overload: a Phase I study in Japan.

Authors:  Keisuke Miyazawa; Kazuma Ohyashiki; Akio Urabe; Tomoko Hata; Shinji Nakao; Keiya Ozawa; Takayuki Ishikawa; Junji Kato; Yoichi Tatsumi; Hiraku Mori; Midori Kondo; Junsuke Taniguchi; Hiromi Tanii; Lisa Rojkjaer; Mitsuhiro Omine
Journal:  Int J Hematol       Date:  2008-07-04       Impact factor: 2.319

  3 in total

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