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Diagnosis and management of thalassaemia.

作者信息

Peters M, Heijboer H, Smiers F, Giordano P C

机构信息

Department of Paediatric Haematology, Emma Children's Hospital, Academic Medical Centre, Amsterdam, Netherlands.

出版信息

BMJ. 2012 Jan 25;344:e228. doi: 10.1136/bmj.e228.

DOI:10.1136/bmj.e228
PMID:22277544
Abstract
摘要

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Diagnosis and management of thalassaemia.地中海贫血的诊断与管理
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Transfusion-associated iron overload as an adverse risk factor for transplantation outcome in patients undergoing reduced-intensity stem cell transplantation for myeloid malignancies.输血相关铁过载作为接受低强度干细胞移植治疗髓系恶性肿瘤患者移植结局的不良风险因素。
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Iron overload is associated with low anti-müllerian hormone in women with transfusion-dependent β-thalassaemia.铁过载与依赖输血的β-地中海贫血女性的抗缪勒管激素水平降低有关。
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Magnetic resonance evaluation of hepatic and myocardial iron deposition in transfusion-independent thalassemia intermedia compared to regularly transfused thalassemia major patients.与定期输血的重型地中海贫血患者相比,中间型非输血依赖型地中海贫血患者肝脏和心肌铁沉积的磁共振评估
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No evidence of cardiac iron in 20 never- or minimally-transfused patients with thalassemia intermedia.20例中间型地中海贫血从未输血或极少输血患者未发现心脏铁沉积证据。
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The heart in transfusion dependent homozygous thalassaemia today--prediction, prevention and management.当今输血依赖型纯合子地中海贫血患者的心脏——预测、预防与管理
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[Thalassemia: therapeutic hopes carried by hepcidin].[地中海贫血:铁调素带来的治疗希望]
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