Genetics and pulmonary medicine. 4. Pulmonary embolism.
作者信息
Laffan M
机构信息
Department of Haematology, Imperial College School of Medicine, Hammersmith Hospital, London, UK.
出版信息
Thorax. 1998 Aug;53(8):698-702. doi: 10.1136/thx.53.8.698.
Abstract
摘要
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本文引用的文献
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Thrombomodulin gene mutations associated with myocardial infarction.与心肌梗死相关的血栓调节蛋白基因突变。
Circulation. 1997 Jul 1;96(1):15-8. doi: 10.1161/01.cir.96.1.15.
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The Leiden Thrombophilia Study (LETS).莱顿血栓形成倾向研究（LETS）。
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A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.一种常见的血栓调节蛋白氨基酸二态性与心肌梗死有关。
Thromb Haemost. 1997 Feb;77(2):248-51.
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Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism.高同型半胱氨酸血症、凝血因子V莱顿突变与未来静脉血栓栓塞风险的相互关系。
Circulation. 1997 Apr 1;95(7):1777-82. doi: 10.1161/01.cir.95.7.1777.
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Low prevalence of factor V:Q506 in 41 patients with isolated pulmonary embolism.41例孤立性肺栓塞患者中因子V：Q506的低患病率。
Thromb Haemost. 1997 Mar;77(3):440-3.
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A prospective study of risk factors for pulmonary embolism in women.一项关于女性肺栓塞危险因素的前瞻性研究。
JAMA. 1997 Feb 26;277(8):642-5.
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The risk of recurrent venous thromboembolism in patients with an Arg506-->Gln mutation in the gene for factor V (factor V Leiden).凝血因子V基因（凝血因子V莱顿）中存在Arg506→Gln突变的患者发生复发性静脉血栓栓塞的风险。
N Engl J Med. 1997 Feb 6;336(6):399-403. doi: 10.1056/NEJM199702063360602.
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Inherited thrombophilia: Part 2.遗传性血栓形成倾向：第2部分。
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