摘要
卒中的基因研究进展很快,新方法和新技术的应用以及致病基因的确定有助于卒中的预防、早期诊断和积极治疗。文章主要介绍了卒中基因研究方面的新进展。
出处
《国外医学（脑血管疾病分册）》
2003年第5期382-383,共2页
Foreign Medical Sciences Cerebrovascular Diseases
参考文献18
-
1Brass LM, Isaacsohn JL, Merikangas KR, et al. A study of twins and stroke. Stroke, 1992, 23:221 -223.
-
2Bak S, Gaist D, Sindrup SH, et al. Genetic liability in stroke: a long-term follow-up study of Danish twins. Stroke. 2002.33:769 - 774.
-
3Liao D, Myers R, Hunt S, et al. Familial history of stroke and stroke risk. The Family Heart Study. Stroke, 1997, 28:1908 - 1912.
-
4Kiely DK, Wolf PA, Cupples LA, et al. Familial aggregation of stroke. The Framingham Study. Stroke, 1993, 24: 1366 - 1371.
-
5Chabriat H, Vahedi IL Iba-Zizen MT, et al. Clinical spectrun of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Lancet,1995, 346:934 -939.
-
6Pulkes T, Sweeney MG, Hanna MG. Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. Lancet,2000, 356:2068 - 2069.
-
7Crutchfield KE, Patronas NJ, Dambrosia JM, et al. Quantitative analysis of cerebral vasculopathy m patients with Fabry disease. Neurology, 1998,50:1746 - 1749.
-
8Zee RY, Ridker PM, Stampfer MJ, et al. Prospective evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of stroke. Circulation, 1999, 99:340 -343.
-
9Elbaz A, Pokier O, Moulm T,et al. Association between the Glu298Asp polymorphism in the endothelial constitutive nitric oxide synthase gene and brain infarction. The GENIC Investigators.Stroke, 2000, 31:1634 - 1639.
-
10Kessler C, Spitzer C, Stauske D, et al. The apolipoprotein E and β-fibrinogen G/A-455 gene polymorphisms are associated with ischemic stroke involving large-vessel disease. Arterioscler Thromb Vase Biol, 1997, 17:2880 - 2884.
同被引文献5
-
1李正仪,石少亭,陈崴,何英利,张玉蓉.FXIIIA3种基因多态性与脑血管疾病的关系[J].中风与神经疾病杂志,2005,22(2):100-103. 被引量：5
-
2Gallivan L, Markham Af, Anwar R, et al. The leu564 factor XIIIA variant results in significantly lower plasma factor XIII levels than the pro564 variant [ J ]. Thromb haelnost, 1999,82 ( 4 ) : 1368-1370.
-
3Reiner AP, Schwartz SM, Frank MB, et al. Polymorphisms of coagulation factor XIII subunit A and risk of nonfatal hemorrhagic stroke in young white women[ J]. Stroke,2001,32( 11 ) :2580-2586,
-
4Lorand L. Factor XIII : structure, activation, and interactions with fibrinogen and fibrin [ J ]. Ann N Y Acad Sci,2001,936:291-311.
-
5Suzuki K, Henke J, Iwata M, et al. Novel polymorphisms and haplotypes in the human coagulation factor III A-subunit gene [ J ]. Hum Genet, 1996,98:393-395.
二级引证文献3
-
1秦培英,唐玉兰,黄芩.脑出血及可干预危险因素与FⅩⅢA Pro564Leu多态性关系[J].中风与神经疾病杂志,2010,27(4):341-344. 被引量：1
-
2唐玉兰,秦培英,黄芩,梁军利.广西地区壮、汉族原发性脑出血患者凝血因子 A亚单位Pro564Leu基因多态性的研究[J].临床神经病学杂志,2011,24(2):102-104. 被引量：3
-
3秦培英,唐玉兰,黄芩.不同性别脑出血与凝血因子ⅩⅢAPro564Leu基因多态性的关系[J].中风与神经疾病杂志,2011,28(9):790-792. 被引量：2
-
1曾益新.与老年性痴呆有关的淀粉样蛋白基因研究进展[J].国外医学（老年医学分册）,1992,13(3):100-102. 被引量：2
-
2竹岛多贺夫,项振家,陈谅.头痛的基因研究进展[J].日本医学介绍,2000,21(12):537-537. 被引量：2
-
3董成龙,程宇琪.ANK3基因与情感障碍的研究进展[J].精神医学杂志,2016,29(3):234-237. 被引量：1
-
4陈唯唯,舒红格,戴慧,张菁.第一部分 中枢神经系统影像学[J].放射学实践,2010,25(G00):1-4.
-
5梁秀龄,陈嵘.遗传性运动障碍疾病的基因研究进展[J].中华神经科杂志,1997,30(1):42-46. 被引量：1
-
6姜树军,匡培根.缺血性脑血管病的基因研究进展[J].国外医学（脑血管疾病分册）,1996,4(2):67-70. 被引量：5
-
7彭继英,孙异临.与帕金森病相关的致病基因研究进展[J].首都医科大学学报,2006,27(2):271-274. 被引量：4
-
8马秋兰,陈彪.阿尔茨海默病早老素-1基因研究进展[J].引进国外医药技术与设备,1999,5(12):44-47. 被引量：1
-
9蔡亚梅,王晓明,冯凯.阿尔茨海默病主要相关基因研究进展[J].医学与哲学（B）,2007,28(11):14-16. 被引量：1
-
10刘东涛,李淑娟,胡文立.缺血性脑血管病的基因研究进展[J].北京医学,2008,30(12):732-734.
