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
相似文献
1
Genetics and pulmonary medicine. 4. Pulmonary embolism.
Thorax. 1998 Aug;53(8):698-702. doi: 10.1136/thx.53.8.698.
2
Inherited thrombophilias.
QJM. 1997 Jun;90(6):375-8. doi: 10.1093/qjmed/90.6.375.
3
Hunting for the mutation in inherited thrombophilia.
Blood Coagul Fibrinolysis. 2004 Mar;15(2):125-7. doi: 10.1097/00001721-200403000-00002.
4
Genetic risk factors for thrombophilia in Japanese.
Rinsho Ketsueki. 2009 May;50(5):381-8.
5
Factor V Leiden mutation in women with idiopathic pulmonary embolism.
Thromb Haemost. 1997 Oct;78(4):1298.
6
[Study of thrombophilia in Japan achieved by the Department of Clinical Chemistry and Laboratory Medicine, Kyushu University].
Fukuoka Igaku Zasshi. 2006 Jan;97(1):1-7.
7
[Familial protein S deficiency].
Tidsskr Nor Laegeforen. 1993 Nov 20;113(28):3464-5.
8
[Congenital thrombophilia].
Rinsho Ketsueki. 2016 Mar;57(3):315-21. doi: 10.11406/rinketsu.57.315.
9
[20210G/A mutation of prothrombin gene in a patient with deep venous thrombosis ad pulmonary embolism without other risk factors of thrombosis].
Arch Bronconeumol. 1999 Dec;35(11):567-70.
10
The molecular genetics of familial venous thrombosis.
Baillieres Clin Haematol. 1994 Sep;7(3):637-74. doi: 10.1016/s0950-3536(05)80102-7.
本文引用的文献
1
Thrombomodulin gene mutations associated with myocardial infarction.
Circulation. 1997 Jul 1;96(1):15-8. doi: 10.1161/01.cir.96.1.15.
2
The Leiden Thrombophilia Study (LETS).
Thromb Haemost. 1997 Jul;78(1):631-5.
3
4
5
A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.
Thromb Haemost. 1997 Feb;77(2):248-51.
6
Interrelation of hyperhomocyst(e)inemia, factor V Leiden, and risk of future venous thromboembolism.
Circulation. 1997 Apr 1;95(7):1777-82. doi: 10.1161/01.cir.95.7.1777.
7
Low prevalence of factor V:Q506 in 41 patients with isolated pulmonary embolism.
Thromb Haemost. 1997 Mar;77(3):440-3.
8
A prospective study of risk factors for pulmonary embolism in women.
JAMA. 1997 Feb 26;277(8):642-5.
9
The risk of recurrent venous thromboembolism in patients with an Arg506-->Gln mutation in the gene for factor V (factor V Leiden).
N Engl J Med. 1997 Feb 6;336(6):399-403. doi: 10.1056/NEJM199702063360602.
10
Inherited thrombophilia: Part 2.
Thromb Haemost. 1996 Dec;76(6):824-34.
Zotero 插件