Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases.
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A. Wu | G. Tsongalis | A. Wu
[1] J. Stokes. Book Review A War of Nerves: Soldiers and Psychiatrists in the Twentieth Century By Ben Shephard. 487 pp., illustrated. Cambridge, Mass., Harvard University Press, 2001. $27.95. 0-674-00592-9 , 2001 .
[2] M. Hirata,et al. Seven DNA polymorphisms at the candidate genes of atherosclerosis in Brazilian women with angiographically documented coronary artery disease. , 2000, Clinica chimica acta; international journal of clinical chemistry.
[3] D. Girelli,et al. Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease. , 2000, The New England journal of medicine.
[4] C. Mirkin,et al. Scanometric DNA array detection with nanoparticle probes. , 2000, Science.
[5] A. Catapano,et al. Low density lipoprotein oxidation, antioxidants, and atherosclerosis , 2000, Current opinion in cardiology.
[6] A. Reiner,et al. Genetic variants of platelet glycoprotein receptors and risk of stroke in young women. , 2000, Stroke.
[7] Jin Q. Kim,et al. Plasminogen activator inhibitor-1 4G/5G promoter polymorphism and coagulation factor VII Arg353-->Gln polymorphism in Korean patients with coronary artery disease. , 2000, Journal of Korean medical science.
[8] B. Damasceno,et al. Inherited Thrombophilia as a Risk Factor for the Development of Ischemic Stroke in Young Adults , 2000, Thrombosis and Haemostasis.
[9] K. Kawazoe,et al. Genetic polymorphism of 5,10‐methylenetetrahydrofolate increases risk of myocardial infarction and is correlated to elevated levels of homocysteine in the Japanese general population , 2000, Coronary artery disease.
[10] G J Tsongalis,et al. Polymorphisms in the genes for coagulation factors II, V, and VII in patients with ischemic heart disease. , 1999, Archives of pathology & laboratory medicine.
[11] A. Carter,et al. Association of the platelet glycoprotein IIb HPA-3 polymorphism with survival after acute ischemic stroke. , 1999, Stroke.
[12] N. Bornstein,et al. The A677V methylenetetrahydrofolate reductase gene polymorphism and carotid atherosclerosis. , 1999, Stroke.
[13] J. Gorący,et al. [C677T gene polymorphism of methylenetetrahydrofolate reductase (MTHFR) in patients with myocardial infarction]. , 1999, Polskie Archiwum Medycyny Wewnetrznej.
[14] M. Margaglione,et al. Inherited prothrombotic conditions and premature ischemic stroke: sex difference in the association with factor V Leiden. , 1999, Arteriosclerosis, thrombosis, and vascular biology.
[15] M. Margaglione,et al. Prothrombotic genetic risk factors in young survivors of myocardial infarction. , 1999, Blood.
[16] I. Bata,et al. Relation of genetic polymorphisms of apolipoprotein E, angiotensin converting enzyme, apolipoprotein B-100, and glycoprotein IIIa and early-onset coronary heart disease. , 1999, Clinical biochemistry.
[17] B. Modan,et al. Synergistic effects of prothrombotic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males. , 1999, Blood.
[18] P. Ridker,et al. G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men. , 1999, Circulation.
[19] A. Kastrati,et al. PlA polymorphism of platelet glycoprotein IIIa and risk of restenosis after coronary stent placement. , 1999, Circulation.
[20] J. Carlquist,et al. Associations between a polymorphism in the gene encoding glycoprotein IIIa and myocardial infarction or coronary artery disease. , 1999, Journal of the American College of Cardiology.
[21] R. Press,et al. Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke. , 1999, Diagnostic molecular pathology : the American journal of surgical pathology, part B.
[22] M. Laule,et al. A1/A2 polymorphism of glycoprotein IIIa and association with excess procedural risk for coronary catheter interventions: a case-controlled study , 1999, The Lancet.
[23] P. Ridker,et al. Factor V Leiden is not a risk factor for myocardial infarction among young women. , 1999, Blood.
[24] D. Coakley,et al. Genetic analysis of the thermolabile variant of 5, 10-methylenetetrahydrofolate reductase as a risk factor for ischemic stroke. , 1999, Arteriosclerosis, thrombosis, and vascular biology.
[25] M. Kaste,et al. Genetic Polymorphism of Platelet Glycoprotein IIIa in Patients with Acute Myocardial Infarction and Acute Ischaemic Stroke , 1999, Journal of cardiovascular risk.
[26] L. Deecke,et al. C677T MTHFR mutation and factor V Leiden mutation in patients with TIA/minor stroke: a case-control study. , 1999, Thrombosis research.
[27] P. Reitsma,et al. The 20210 G → A mutation in the 3′‐untranslated region of the prothrombin gene and the risk for arterial thrombotic disease , 1999, British journal of haematology.
[28] F. Burzotta,et al. The 4G/5G Polymorphism of PAI-1 Promoter Gene and the Risk of Myocardial Infarction: A Meta-analysis , 1998, Thrombosis and Haemostasis.
[29] Y. Yazaki,et al. Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke in Japanese. , 1998, Arteriosclerosis, thrombosis, and vascular biology.
[30] J. Stricker,et al. Association of the Platelet Glycoprotein IIIa PIA1/A2 Gene Polymorphism to Coronary Artery Disease but not to Nonfatal Myocardial Infarction in Low Risk Patients , 1998, Thrombosis and Haemostasis.
[31] M. Delgado-Rodríguez,et al. Polymorphism of the Platelet Glycoprotein IIIa Gene in Patients with Coronary Stenosis , 1998, Thrombosis and Haemostasis.
[32] P. Chiusolo,et al. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. , 1998, Blood.
[33] M. Roden,et al. Inherited platelet glycoprotein polymorphisms and a risk for coronary heart disease in young central Europeans. , 1998, Thrombosis research.
[34] T. Arinami,et al. Methylenetetrahydrofolate reductase and apolipoprotein E polymorphisms are independent risk factors for coronary heart disease in Japanese: a case-control study. , 1998, Atherosclerosis.
[35] T. Raghunathan,et al. Risk of stroke in young women and two prothrombotic mutations: factor V Leiden and prothrombin gene variant (G20210A) , 1998, Stroke.
[36] P. de Knijff,et al. Polymorphisms in the coagulation factor VII gene and the risk of myocardial infarction. , 1998, The New England journal of medicine.
[37] D. Ardissino,et al. The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[38] J. Carlquist,et al. A mutation in the methylenetetrahydrofolate reductase gene is not associated with increased risk for coronary artery disease or myocardial infarction. , 1997, Journal of the American College of Cardiology.
[39] A. Carter,et al. Association of the Platelet PlA Polymorphism of Glycoprotein IIb/IIIa and the Fibrinogen Bβ 448 Polymorphism With Myocardial Infarction and Extent of Coronary Artery Disease , 1997 .
[40] F R Rosendaal,et al. A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. , 1997, Blood.
[41] H. Markus,et al. A common polymorphism in the methylenetetrahydrofolate reductase gene, homocysteine, and ischemic cerebrovascular disease. , 1997, Stroke.
[42] T. Raghunathan,et al. Myocardial infarction in young women in relation to plasma total homocysteine, folate, and a common variant in the methylenetetrahydrofolate reductase gene. , 1997, Circulation.
[43] T. Raghunathan,et al. Factor V Leiden (resistance to activated protein C) increases the risk of myocardial infarction in young women. , 1997, Blood.
[44] Y. Yazaki,et al. Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease. , 1997, Circulation.
[45] P. Ridker,et al. Inflammation, aspirin, and the risk of cardiovascular disease in apparently healthy men. , 1997, The New England journal of medicine.
[46] P. Frosst,et al. Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease. , 1997, Arteriosclerosis, thrombosis, and vascular biology.
[47] P. Ridker,et al. PIA1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke, and venous thrombosis , 1997, The Lancet.
[48] B. Giusti,et al. Prevalence of Factor V Leiden Mutation in Non-European Populations , 1997, Thrombosis and Haemostasis.
[49] W. Willett,et al. Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians. , 1996, Circulation.
[50] A. Carter,et al. Platelet glycoprotein IIIa PIA polymorphism in young men with myocardial infarction , 1996, The Lancet.
[51] J. Weiss,et al. A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis. , 1996, The New England journal of medicine.
[52] S. Devaraj,et al. Low-density lipoprotein oxidation, antioxidants, and atherosclerosis: a clinical biochemistry perspective. , 1996, Clinical chemistry.
[53] D. Arveiler,et al. Factor VII Arg/Gln353 polymorphism determines factor VII coagulant activity in patients with myocardial infarction (MI) and control subjects in Belfast and in France but is not a strong indicator of MI risk in the ECTIM study. , 1996, Atherosclerosis.
[54] P. Ridker,et al. Factor V Leiden and risks of recurrent idiopathic venous thromboembolism. , 1995, Circulation.
[55] P. Ridker,et al. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. , 1995, The New England journal of medicine.
[56] B. Winkelmann,et al. Mutation in coagulation factor V associated with resistance to activated protein C in patients with coronary artery disease , 1995, The Lancet.
[57] A. Evans,et al. Myocardial infarction, Arg 506 to Gin factor V mutation, and activated protein C resistance , 1995, The Lancet.
[58] J. Mckenney,et al. Summary of the second report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II) , 1993, JAMA.
[59] M. Malinow,et al. Homocyst(e)ine and coronary artery disease , 1992 .
[60] R. Lawn,et al. Lipoprotein(a) and atherosclerosis. , 1991, Annals of internal medicine.
[61] Young Women. , 1875, Hall's journal of health.
[62] P. Renshaw,et al. [Detection, evaluation, and treatment of high blood cholesterol in adults]. , 2001, Revista panamericana de salud publica = Pan American journal of public health.
[63] S. Ishibashi,et al. Lipoprotein(a) and atherosclerosis. , 2001, Arteriosclerosis, thrombosis, and vascular biology.
[64] F R Rosendaal,et al. Risk of Myocardial Infarction Associated With Factor V Leiden or Prothrombin Interaction of Coagulation Defects and Cardiovascular Risk Factors : Increased , 1998 .
[65] T. Matsuo,et al. [Activated protein C resistance]. , 1998, Ryoikibetsu shokogun shirizu.
[66] M. Pinotti,et al. Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma. , 1996, Arteriosclerosis, thrombosis, and vascular biology.
[67] R. Press,et al. Ischemic stroke in the elderly. Role of the common factor V mutation causing resistance to activated protein C. , 1996, Stroke.
[68] R. Matthews,et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase , 1995, Nature Genetics.