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Iron overload in transfusion-dependent survivors of hemoglobin Bart's hydrops fetalis.

作者信息

Amid Ali, Chen Shiyi, Athale Uma, Charpentier Karen, Merelles-Pulcini Manuela, Odame Isaac, Kirby-Allen Melanie

机构信息

Division of Hematology/Oncology, Children's Hospital of Eastern Ontario, Ottawa, ON

Department of Pediatrics, University of Ottawa, Ottawa, ON.

出版信息

Haematologica. 2018 May;103(5):e184-e187. doi: 10.3324/haematol.2017.178368. Epub 2018 Jan 25.

Abstract
摘要

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本文引用的文献

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An international registry of survivors with Hb Bart's hydrops fetalis syndrome.
Blood. 2017 Mar 9;129(10):1251-1259. doi: 10.1182/blood-2016-08-697110. Epub 2017 Jan 5.
3
Optimizing chronic transfusion therapy for survivors of hemoglobin Barts hydrops fetalis.
Blood. 2016 Mar 3;127(9):1208-11. doi: 10.1182/blood-2015-10-673889. Epub 2016 Jan 5.
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Hepcidin is suppressed by erythropoiesis in hemoglobin E β-thalassemia and β-thalassemia trait.
Blood. 2015 Jan 29;125(5):873-80. doi: 10.1182/blood-2014-10-606491. Epub 2014 Dec 17.
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Iron metabolism: interactions with normal and disordered erythropoiesis.
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Liver iron concentrations and urinary hepcidin in beta-thalassemia.
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