[1]Ashild O, Eva G, Ulrike W, et al. Prevalence and covariates of uncontrolled hypertension in ischemic stroke survivors: the Norwegian stroke in the young study[J]. Blood Press, 2018, 27(3):1-8.
[2]马芳芳,谢华斌. MTHFR基因C677T多态性与中国人群冠心病相关性的Meta分析[J]. 临床心血管病杂志, 2018, 34(10):32-36.
[3]Hoffman A, Taleski G, Qian H, et al. Methylenetetrahydrofolate reductase deficiency deregulates regional brain amyloid-β protein precursor expression and phosphorylation levels[J]. J Alzheimers Dis, 2018, 28(6):488-489.
[4]朱娟娟,唐吉斌.亚甲基四氢叶酸还原酶基因多态性分析的临床应用[J].分子诊断与治疗杂志,2018,10(6):361-366.
[5]刘丹琦,盛阳昊,王萍,等.5,10-亚甲基四氢叶酸还原酶基因多态性与不育不孕症相关性研究进展[J].中国临床药理学与治疗学,2015,20(2):235-240.
[6]李建平,卢新政,霍勇,等.H型高血压诊断与治疗专家共识[J].中国医学前沿杂志(电子版),2016,8(5):23-28.
[7]李建平,霍勇,刘平,等.马来酸依那普利叶酸片降压、降同型半胱氨酸的疗效和安全性[J].北京大学学报(医学版),2007(6):614-618.
[8]Wang XM, Fu JJ, Li QX, et al. Geographical and ethnic distributions of the MTHFR C677T, A1298C and MTRR A66G gene polymorphisms in Chinese populations: A meta-analysis[J]. PLOS ONE, 2016, 11(4):e0152414.
[9]范超,陈鸣,邓少丽,等.重庆地区脑卒中患者Hcy水平及MTHFRC677T基因多态性研究[J].重庆医学,2016,45(35):4932-4937.
[10]张海洋, 张金华, 张会敏. MTHFR基因多态性与脑卒中的相关性[J]. 中国老年学杂志, 2012, 32(4):690-691.
[11]王超, 于莲, 季方茹, 等. MTHFR基因多态性在黑龙江东部地区脑卒中患者的频率分析[J]. 黑龙江医药科学,2017,40(4):48-50.
[12]于小琪, 秦琴保, 王双艳, 等. MTHFR基因多态性与广州市老年人缺血性脑卒中的相关性[J]. 实用医学杂志, 2016,32(21):3540-3542.
[13]王陇德,刘建民,杨弋,等.《中国脑卒中防治报告2017》概要[J].中国脑血管病杂志,2018,15(11):611-617.
[14]Abhinand PA, Manikandan M, Mahalakshmi R, et al. Meta-analysis study to evaluate the association of MTHFR C677T polymorphism with risk of ischemic stroke[J]. Bioinformation, 2017, 13(6):214-219.
[15]栾迪,丁言运,王雅平,等.皖南地区脑卒中人群亚甲基四氢叶酸还原酶基因多态性特点分析[J].皖南医学院学报,2019,38(3):227-230.
[16]黄武,邱晓敏,万小亮,等.佛山汉族高血压患者亚甲基四氢叶酸还原酶基因的分布[J].广东医学,2016,37(23):3524-3526.
[17]Rai, Vandana. Methylenetetrahydrofolate reductase C677T polymorphism and recurrent pregnancy loss risk in Asian population: A meta-analysis[J]. Indian J Clin Biochem, 2016, 31(4):402-413.
[18]Mao R, Fan Y, Chen F, et al. Methylenetetrahydrofolate reductase gene polymorphisms in 13 Chinese ethnic populations[J]. Cell Biochemistry Funct, 2008, 26(3):352-358.
[19]Wenxing L,Fei C,Ajie Z, et al. Folate deficiency and gene polymorphisms of MTHFR, MTR and MTRR elevate the hyperhomocysteinemia risk[J]. Clin Lab, 2017, 63(3):523-533.
[20]叶小春,韩勇,朱峰,等.H型高血压伴MTHFR基因突变的药学监护[J].医药导报,2017,36(4):403-405. |