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059 The C677T mutation of the methylenetetrahydrofolate reductase gene is not associated with the risk of myocardial infarction among Tunisian male patients

机译：059在突尼斯男性患者中，亚甲基四氢叶酸还原酶基因的C677T突变与心肌梗死的风险无关

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Sami Mourali Mohamed; Kallel Amani; Sdiri Yossra; Abdessalem Salem; Zaroui Amira; Fakih Moncef; Mechmeche Rachid; Jemaa Riadh; Kaabachi Naziha;
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1. Association of methylenetetrahydrofolate reductase C677T and A1298C polymorphisms with myocardial infarction in Tunisian young patients [J] . Dhouha Berredjeb Ben Slama, Najiba Fekih Mrissa, Abdeddayem Haggui, Comparative clinical pathology . 2014,第5期

机译：突尼斯青年患者中亚甲基四氢叶酸还原酶C677T和A1298C多态性与心肌梗死的关系
2. Recurrent Myocardial Infarction Despite Normal C-reactive Protein in a Patient with Behcet’s Disease and Compound Heterozygous Methylenetetrahydrofolate Reductase (MTHFR) Mutations (C677T and A1298C) [J] . Muhammad Hamza Saad Shaukat, Aixa Toledo-Garcia, Mikhail Torosoff Cureus. . 2019,第8期

机译：Behcet病和复合杂合亚甲基四氢叶酸还原酶（MTHFR）突变（C677T和A1298C）患者，尽管C反应蛋白正常，但复发性心肌梗塞
3. Methylenetetrahydrofolate Reductase C677T and Platelet Glycoprotein IIb/IIIa Genes Polymorphism in Myocardial Infarction Egyptian Patients in Ismailia City [J] . Kefah H Ali, Nagwan A Sabek, Loaa A Tag Eldeen, American Journal of Biomedical Research . 2016,第3期

机译：亚甲基四氢叶酸还原酶C677T和血小板糖蛋白IIb / IIIa基因多态性在埃及伊斯梅利亚市心肌梗死患者中
4. C677T Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism and Treatment Response in Schizophrenia Patients [C] . Muthmainah Muthmainah, Nova Kurniasari, Mohammad Fanani, Health Science International Conference . 2017

机译：C677T甲基四乙烯酸还原酶（STHFR）基因多态性和精神分裂症患者的治疗反应
5. Selective cyclooxygenase-2 (COX-2) inhibition and risk of acute myocardial infarction or stroke in a population of rheumatoid arthritis and osteoarthritis patients from an administrative medical claims dataset. [D] . Spalding, William Michael. 2003

机译：来自行政医疗索赔数据集的类风湿关节炎和骨关节炎患者群体中的选择性环氧合酶2（COX-2）抑制和急性心肌梗塞或中风的风险。
6. Recurrent Myocardial Infarction Despite Normal C-reactive Protein in a Patient with Behcet’s Disease and Compound Heterozygous Methylenetetrahydrofolate Reductase (MTHFR) Mutations (C677T and A1298C) [O] . Muhammad Hamza Saad Shaukat, Aixa Toledo-Garcia, Mikhail Torosoff -1

机译：Behcet病和复合杂合亚甲基四氢叶酸还原酶（MTHFR）突变（C677T和A1298C）患者尽管C反应蛋白正常但复发性心肌梗塞
7. Recurrent Myocardial Infarction Despite Normal C-reactive Protein in a Patient with Behcet’s Disease and Compound Heterozygous Methylenetetrahydrofolate Reductase (MTHFR) Mutations (C677T and A1298C) [O] . Muhammad Hamza Saad Shaukat, Aixa Toledo-Garcia, Mikhail Torosoff 2019

机译：尽管Behcet疾病的患者常规C反应蛋白和化合物杂合甲基四氢脱乙酸盐酸还原酶（MTHFR）突变（C677T和A1298C），但常见的心肌梗死。

059 The C677T mutation of the methylenetetrahydrofolate reductase gene is not associated with the risk of myocardial infarction among Tunisian male patients

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