镰状细胞-β地中海贫血合并甲型血友病：一种罕见的表现。 - Suppr

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超能文献

Sickle cell-β thalassemia with concomitant hemophilia A: a rare presentation.

作者信息

Dhiman Pratibha, Chaudhary Rahul, Sudha Krishna

机构信息

Department of Hematology, Institute of Liver and Biliary Sciences, New Delhi, India.

Department of Pathology, ESI Hospital, New Delhi, India.

出版信息

Blood Res. 2015 Dec;50(4):264-7. doi: 10.5045/br.2015.50.4.264. Epub 2015 Dec 21.

DOI:10.5045/br.2015.50.4.264

PMID:26770958

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4705056/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b68/4705056/c9bb78544742/br-50-264-g001.jpg

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本文引用的文献

Prevalence of β-thalassemia and other haemoglobinopathies in six cities in India: a multicentre study.印度六个城市β地中海贫血及其他血红蛋白病的患病率：一项多中心研究

J Community Genet. 2013 Jan;4(1):33-42. doi: 10.1007/s12687-012-0114-0. Epub 2012 Oct 21.

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India.印度西部镰状细胞-β地中海贫血的临床、血液学及分子变异性

Indian J Hum Genet. 2010 Sep;16(3):154-8. doi: 10.4103/0971-6866.73410.

Hypercoagulability and thrombotic complications in hemolytic anemias.溶血性贫血中的高凝状态和血栓并发症。

Haematologica. 2009 Nov;94(11):1481-4. doi: 10.3324/haematol.2009.013672.

Prenatal diagnosis in a family at risk for beta-thalassemia and hemophilia A: an uncommon association.一个有β地中海贫血和甲型血友病风险的家庭中的产前诊断：一种罕见的关联。

Hemoglobin. 2004;28(4):343-6. doi: 10.1081/hem-200037719.

The hypercoagulable state in thalassemia.地中海贫血中的高凝状态。

Blood. 2002 Jan 1;99(1):36-43. doi: 10.1182/blood.v99.1.36.

Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors.儿童期严重甲型血友病的症状性发作取决于血栓形成前危险因素的存在。

Thromb Haemost. 2001 Feb;85(2):218-20.

Wilson's disease with concomitant beta thalassaemia and factor V deficiency.威尔逊氏病合并β地中海贫血和凝血因子V缺乏症。

Ital J Gastroenterol Hepatol. 1998 Dec;30(6):633-5.

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