Iron-chelating therapy and the treatment of thalassemia

NF Olivieri, GM Brittenham - … Journal of the American Society of …, 1997 - ashpublications.org
(BM) expansion, permit normal development throughout childhood, and extend survival. 1 In
parallel, transfusions re- Early studies of the use of neocytes, or young RBCs, sult in a …

Intramuscular desferrioxamine in patients with Alzheimer's disease

DRC McLachlan, TPA Kruck, W Kalow, DF Andrews… - The Lancet, 1991 - Elsevier
Although epidemiological and biochemical evidence suggests that aluminium may be
associated with Alzheimer's disease (AD), there is no convincing proof of a causal link for …

Cardiovascular function and treatment in β-thalassemia major: a consensus statement from the American Heart Association

DJ Pennell, JE Udelson, AE Arai, B Bozkurt… - Circulation, 2013 - Am Heart Assoc
This aim of this statement is to report an expert consensus on the diagnosis and treatment of
cardiac dysfunction in β-thalassemia major (TM). This consensus statement does not cover …

[HTML][HTML] Survival in medically treated patients with homozygous β-thalassemia

NF Olivieri, DG Nathan, JH MacMillan… - … England Journal of …, 1994 - Mass Medical Soc
Background The prognosis of patients with homozygous β-thalassemia (thalassemia major)
has been improved by transfusion and iron-chelation therapy. We analyzed outcome and …

Iron-chelating therapy for transfusional iron overload

GM Brittenham - New England Journal of Medicine, 2011 - Mass Medical Soc
Iron-Chelating Therapy for Transfusional Iron Overload | New England Journal of Medicine Skip
to main content The New England Journal of Medicine homepage Advanced Search SEARCH …

Comparison of effects of oral deferiprone and subcutaneous desferrioxamine on myocardial iron concentrations and ventricular function in beta-thalassaemia

LJ Anderson, B Wonke, E Prescott, S Holden… - The Lancet, 2002 - thelancet.com
Background Despite the introduction of the parenteral iron chelator desferrioxamine more
than 30 years ago, 50% of patients with thalassaemia major die before the age of 35 years …

Secondary iron overload

JP Kushner, JP Porter, NF Olivieri - ASH Education Program …, 2001 - ashpublications.org
Transfusion therapy for inherited anemias and acquired refractory anemias both improves
the quality of life and prolongs survival. A consequence of chronic transfusion therapy is …

Design of iron chelators with therapeutic application

ZD Liu, RC Hider - Coordination Chemistry Reviews, 2002 - Elsevier
Iron overload is a serious clinical condition which can be largely prevented by the use of iron-
specific chelating agents. Desferrioxamine-B, the most widely used iron chelator in …

Design of clinically useful iron (III)‐selective chelators

ZD Liu, RC Hider - Medicinal research reviews, 2002 - Wiley Online Library
Iron overload is a serious clinical condition which can be largely prevented by the use of iron‐
specific chelating agents. Desferrioxamine‐B, the most widely used iron chelator in …

Iron-chelation therapy with oral deferiprone in patients with thalassemia major

NF Olivieri, GM Brittenham, D Matsui… - … England Journal of …, 1995 - Mass Medical Soc
Background To determine whether the orally active iron chelator deferiprone (1, 2-dimethyl-
3-hydroxypyridin-4-one) is efficacious in the treatment of iron overload in patients with …