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Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.

作者信息

Alatri A, Franchi F, Moia M

出版信息

Thromb Haemost. 1998 Dec;80(6):1028-9.

PMID:9869180
Abstract
摘要

相似文献

1
Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.无血栓栓塞事件的纯合子G20210A凝血酶原基因突变：病例报告
Thromb Haemost. 1998 Dec;80(6):1028-9.
2
Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.凝血酶原基因中与严重静脉血栓形成疾病相关的纯合子G20210A转变：一个法国家庭中的两例病例。
Thromb Haemost. 1998 Dec;80(6):1027-8.
3
Coagulation factor II activity determination is not useful as a screening tool for the G20210A prothrombin gene allele.
Thromb Haemost. 2000 Jul;84(1):141-2.
4
The VITA project: prothrombin G20210A mutation and venous thromboembolism in the general population.VITA项目：普通人群中的凝血酶原G20210A突变与静脉血栓栓塞
Thromb Haemost. 1999 Nov;82(5):1395-8.
5
Mutation screening for thrombophilia: two cases with factor V Cambridge without activated protein C resistance.血栓形成倾向的突变筛查：两例无活化蛋白C抵抗的因子V剑桥突变病例
Thromb Haemost. 2002 May;87(5):919-20.
6
What clinical significance has the presence of the homozygous G20210A prothrombin gene mutation in a healthy woman?
Thromb Haemost. 2000 Aug;84(2):355-6.
7
Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.
Haematologica. 2005 Nov;90 Suppl:ECR30.
8
Prevalence of the prothrombin gene 20210A mutation in thrombophilic and healthy Algerian subjects.阿尔及利亚血栓形成倾向患者及健康人群中凝血酶原基因20210A突变的患病率
Thromb Haemost. 1999 Nov;82(5):1554-5.
9
G20210A prothrombin gene variant and clinical outcome in patients with a first acute coronary syndrome.G20210A凝血酶原基因变异与首次急性冠脉综合征患者的临床结局
Haematologica. 2004 Sep;89(9):1134-8.
10
The prothrombin G20210A mutation is a risk factor for sudden hearing loss in young patients.
Thromb Haemost. 2001 Oct;86(4):1118-9.

引用本文的文献

1
Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.凝血酶原G20210A基因突变所致复发性深静脉血栓形成和肺栓塞：病例报告及文献复习
J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096211058486. doi: 10.1177/23247096211058486.
2
Bilateral Superficial Femoral Artery Thrombosis in a 15-Year-Old Caucasian Male with Homozygous Prothrombin G20210A Genotype and Associated Antiphospholipid Syndrome.一名15岁白种男性，患有纯合子凝血酶原G20210A基因型及相关抗磷脂综合征，出现双侧股浅动脉血栓形成
Int J Angiol. 2016 Dec;25(5):e100-e105. doi: 10.1055/s-0035-1548557. Epub 2015 Mar 23.
3
Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype. A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology.
纯合子凝血酶原20210AA基因型患者的表型异质性。一篇来自2005年威廉·博蒙特医院分子病理学研讨会的论文。
J Mol Diagn. 2006 Sep;8(4):420-5. doi: 10.2353/jmoldx.2006.060014.