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The management of patients with Cooley's anemia: transfusions and splenectomy.

作者信息

Piomelli S

机构信息

Pediatric Hematology/Oncology Division, Babies and Children's Hospital of New York, NY 10032, USA.

出版信息

Semin Hematol. 1995 Oct;32(4):262-8.

PMID:8560283
Abstract
摘要

相似文献

1
The management of patients with Cooley's anemia: transfusions and splenectomy.库利贫血患者的管理:输血与脾切除术
Semin Hematol. 1995 Oct;32(4):262-8.
2
Desferrioxamine therapy induces clearance of iron deposits after bone marrow transplantation for thalassemia: case report.
Bone Marrow Transplant. 1993;12 Suppl 1:108-10.
3
Iron removal in ex-thalassemics after BMT: preliminary results from the phlebotomy program. Italian Cooperative Group for Phlebotomy in Ex-thalassemic.异基因造血干细胞移植后地中海贫血患者的铁去除:放血疗法项目的初步结果。意大利地中海贫血放血疗法合作组
Bone Marrow Transplant. 1993;12 Suppl 1:105.
4
Management of cardiac complications in patients with thalassemia major.重型地中海贫血患者心脏并发症的管理
Semin Hematol. 1995 Oct;32(4):288-96.
5
The treatment of Cooley's anemia.
Haematologica. 1990 Sep-Oct;75 Suppl 5:57-65.
6
Management of thalassemia major (Cooley's anemia).重型地中海贫血(库利贫血)的管理
Hematol Oncol Clin North Am. 1991 Jun;5(3):557-69.
7
Outcome of thalassemia treated with conventional therapy.采用传统疗法治疗地中海贫血的结果。
Bone Marrow Transplant. 1993;12 Suppl 1:2-4.
8
Methods for noninvasive measurement of tissue iron in Cooley's anemia.库利贫血中组织铁的非侵入性测量方法。
Ann N Y Acad Sci. 2005;1054:358-72. doi: 10.1196/annals.1345.044.
9
Echocardiographic study in ex-thalassemic patients with iron overload, preliminary observations during phlebotomy therapy.
Bone Marrow Transplant. 1993;12 Suppl 1:106-7.
10
[Splenectomy and blood transfusion in Cooley's disease].
Riv Emoter Immunoematol. 1962;9:43-6.

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Early detection of myocardial dysfunction in poorly treated pediatric thalassemia children and adolescents: Two Saudi centers experience.
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Atypical femoral fracture in a beta-thalassemia major patient with previous bisphosphonate use: case report and a review of the literature.一名曾使用双膦酸盐的重型β地中海贫血患者发生非典型股骨骨折:病例报告及文献综述
J Musculoskelet Neuronal Interact. 2016 Mar;16(1):75-8.
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Iron overload in Beta thalassaemia major and intermedia patients.重型和中间型β地中海贫血患者的铁过载
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Anemia, ineffective erythropoiesis, and hepcidin: interacting factors in abnormal iron metabolism leading to iron overload in β-thalassemia.贫血、无效红细胞生成和铁调素:导致β-地中海贫血中铁过载的异常铁代谢中的相互作用因素。
Hematol Oncol Clin North Am. 2010 Dec;24(6):1089-107. doi: 10.1016/j.hoc.2010.08.003. Epub 2010 Oct 15.
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Bone disease in thalassemia: a frequent and still unresolved problem.地中海贫血中的骨病:一个常见且仍未解决的问题。
J Bone Miner Res. 2009 Mar;24(3):543-57. doi: 10.1359/jbmr.080505.