Coagulation factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T gene mutations do not play a major role in symptomatic neonatal arterial ischaemic stroke

Arnaez Juan; Arca Gemma; Martin-Ancel Ana; Garcia-Alix Alfredo

首页> 外文期刊>British Journal of Haematology >Coagulation factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T gene mutations do not play a major role in symptomatic neonatal arterial ischaemic stroke

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Coagulation factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T gene mutations do not play a major role in symptomatic neonatal arterial ischaemic stroke

机译：凝血因子V G1691A，因子II G20210A和甲基四乙烯醇还原酶C677T基因突变在症状新生儿动脉缺血性中风中不起作用主要作用

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来源
《British Journal of Haematology》 |2018年第2期|共3页
作者
Arnaez Juan; Arca Gemma; Martin-Ancel Ana; Garcia-Alix Alfredo;
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作者单位

Burgos Univ Hosp Dept Neonatol Burgos Spain;

Clin Maternitat Univ Hosp Dept Neonatol Barcelona Spain;

Barcelona Univ St Joan Deu Hosp Paediat Res Inst Barcelona Spain;

Barcelona Univ St Joan Deu Hosp Paediat Res Inst Barcelona Spain;

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原文格式 PDF
正文语种 eng
中图分类血液及淋巴系疾病;
关键词
stroke; arterial infarct; thrombophilia; neonatal haematology; neonate;

机译：中风;动脉梗塞;血栓性;新生儿血液学;新生儿;

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1. Coagulation factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T gene mutations do not play a major role in symptomatic neonatal arterial ischaemic stroke [J] . Arnaez Juan, Arca Gemma, Martin-Ancel Ana, British Journal of Haematology . 2018,第2期

机译：凝血因子V G1691A，因子II G20210A和甲基四乙烯醇还原酶C677T基因突变在症状新生儿动脉缺血性中风中不起作用主要作用
2. The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with p-thalassemia major [J] . Suleimman A. Al Sweedan, Said Jaradat, Muna lraqi, Blood coagulation & fibrinolysis: an international journal in haemostasis and thrombosis . 2009,第8期

机译：约旦重度地中海贫血患者中V因子Leiden（G1691A），凝血酶原G20210A和亚甲基四氢叶酸还原酶C677T突变的患病率
3. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behcet's disease. [J] . Toydem-r PB, Elhan AH, Tukun A, The Journal of rheumatology . 2000,第12期

机译：V因子基因G1691A，亚甲基四氢叶酸还原酶基因C677T和凝血酶原基因G20210A突变对贝塞特病深静脉血栓形成的影响。
4. First thromboemboiic Onset In Children carrying either the heterozygeous Factor V G16911 Mutation or the Prethrembin G20210A Variant [C] . A. Kosch, S. Becker, K:~Kurnik, Hemophilie-Symposion . 2003

机译：携带杂合因子V G16911突变或妊娠期G20210A变体的第一次血栓发病
5. The expression of the constitutively active epidermal growth factor receptor variant III in ovarian cancer cells plays a role in cell dissociation. [D] . Zeineldin, Reema Ramadan. 2003

机译：组成型活性表皮生长因子受体变体III在卵巢癌细胞中的表达在细胞解离中起作用。
6. PlA2 Polymorphism of Platelet Glycoprotein IIb/IIIa and C677T Polymorphism of Methylenetetrahydrofolate Reductase (MTHFR) but Not Factor V Leiden and Prothrombin G20210A Polymorphisms Are Associated with More Severe Forms of Legg–Calvé–Perthes Disease [O] . María Dolores García-Alfaro, María Isabel Pérez-Nuñez, María Teresa Amigo, 2021

机译：血小板糖蛋白IIB / IIIa和C677T多态性的PLA2多态性亚甲基丙酸盐还原酶（MTHFR）但不是因子V赖恩和凝血酶原G20210A多态性与更严重的乳糜腿 - 腐败疾病相关
7. Association of Factor II G20210A, Factor V G1691A and methylenetetrahydrofolate reductase C677T gene polymorphism with different forms of myocardial infarction: ST segment elevation and non-ST segment elevation [O] . Milica Cucuz-Jokic, Vesna Ilic, Bojana Cikota-Aleksic, 2020

机译：因子II G20210A，因子v G1691A和亚甲基四氢呋喃还原酶C677T基因多态性，不同形式的心肌梗死：ST分段升高和非ST段仰角

Coagulation factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T gene mutations do not play a major role in symptomatic neonatal arterial ischaemic stroke

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