Methylene tetrahydrofolate reductase gene and coronary artery disease
Iqbal, M.P.; Frossard, P.M.
Jpma. Journal of the Pakistan Medical Association 53(1): 33-36
2003
ISSN/ISBN: 0030-9982 PMID: 12666851 Document Number: 555087
Document emailed within 1 workday
Related Documents
Eikelboom, J.W.; Saharay, I.; Baker, R.I.; Hankey, G.J. 1998: Methylene tetrahydrofolate reductase mutation and stroke in a monozygotic twin Australian and New Zealand Journal of Medicine 28(6): 849-850Trimarchi, H.án.; Genoud, V.; Schiel, A.; Castañon, M.; Freixas, E.; Diaz, M.L.; Schropp, J.; Martino, D.; Pereyra, H.; Kordich, L. 2002: The C677T thermolabile variant of methylene tetrahydrofolate reductase on homocysteine, folate and vitamin B12 in a hemodialysis center Medicina 62(2): 149-153
Dalal, A.B.; Tewari, D.; Tewari, S.; Sharma, M.K.; Pradhan, M.; Gupta, U.Rani.; Sinha, N.; Agarwal, S. 2006: Association of coronary artery disease with polymorphisms of angiotensin-converting enzyme and methylenetetrahydrofolate reductase gene Indian Heart Journal 58(4): 330-335
Valantine, H.A.; Schroeder, J.S. 1997: HMG-CoA reductase inhibitors reduce transplant coronary artery disease and mortality: evidence for antigen-independent mechanisms? Circulation 96(5): 1370-1373
Wu, N-qiong.; Song, L.; Hua, Y-hong.; Lu, X-feng.; Ye, J.; Li, J-xin.; Gu, D-feng.; Yang, Y-jin. 2008: Association between single nucleotide polymorphisms of matrix metalloproteinase-3 gene and the severity of coronary atherosclerosis in patients with coronary artery disease Zhonghua Xin Xue Guan Bing Za Zhi 36(6): 501-505
Letonja, M.; Peterlin, B.; Bregar, D.; Petrovic, D. 2005: Are the T/C polymorphism of the CYP17 gene and the tetranucleotide repeat (TTTA) polymorphism of the CYP19 gene genetic markers for premature coronary artery disease in Caucasians? Folia Biologica 51(3): 76-81
Halim, S.A.; Wang, A.; Harrison, J.K. 2011: Anomalous right coronary artery origin from the pulmonary artery (ARCAPA) coexisting with obstructive atherosclerotic disease of the left coronary artery Journal of Invasive Cardiology 23(1): E260-E261
Mendonça, M.I.; Dos Reis, R.P.; Freitas, A.I.; Sousa, A.C.; Pereira, A.; Faria, P.; Gomes, S.; Silva, B.; Santos, N.; Serrão, M.; Ornelas, I.íd.; Freitas, S.ón.; Araújo, J.é J.; Brehm, A.ón.; Cardoso, A.A. 2008: Human paraoxonase gene polymorphisms and coronary artery disease risk Revista Portuguesa de Cardiologia: Orgao Oficial da Sociedade Portuguesa de Cardiologia 27(12): 1539-1555
Yu, J.; Han, J.; Mao, J.; Guo, L.; Gao, W. 2014: Association between serum uric acid level and the severity of coronary artery disease in patients with obstructive coronary artery disease Chinese Medical Journal 127(6): 1039-1045
Savchenko, A.P.; Akchurin, R.S.; Rudenko, B.A.; Shiriaev, A.A.; Cherkavskaia, O.V.; Kozlov, G.V. 2010: Long-term follow-up use of "cypher" sirolimus-eluting stents in patients with coronary heart disease after coronary artery bypass grafting with occlusive lesions of the coronary artery Vestnik Rentgenologii i Radiologii 4: 4-12
Jim, M.-H.; Siu, C.-W.; Ho, H.-H.; Miu, R.; Lee, S.W.-L. 2004: Anomalous origin of the right coronary artery from the left coronary sinus is associated with early development of coronary artery disease Journal of Invasive Cardiology 16(9): 466-468
Seyyed Mohammad Reza Kazemi-Bajestani; Ghayour, M.-Mobarhan; Ebrahimi, M.; Moohebati, M.; Habib-Esmaeili, A.; Gordon A. A. Ferns 2007: C-reactive Protein Associated with Coronary Artery Disease in Iranian Patients with Angiographically Defined Coronary Artery Disease Clinical Laboratory 53(1-2): 49-56
Ferrières, J.; Lambert, J.; Lussier-Cacan, S.; Davignon, J. 1995: Coronary artery disease in heterozygous familial hypercholesterolemia patients with the same LDL receptor gene mutation Circulation 92(3): 290-295
Liu, R.; Zhang, Y. 2011: G1359A Polymorphism in the Cannabinoid Receptor-1 Gene is Associated with Coronary Artery Disease in the Chinese Han Population Clinical Laboratory 57(9-10): 689-693
Anvari, A.; Janisiw, M.; Türel, Z.; Huber, K.; Fischer, G.; Panzer, S. 2000: Platelet glycoprotein Ia gene dimorphism alpha2-807 in malignant arrhythmia in coronary artery disease Thrombosis Research 98(4): 281-286
Girisha, K.M.; Gilmour, A.; Mastana, S.; Singh, V.P.; Sinha, N.; Tewari, S.; Ramesh, V.; Sankar, V.H.; Agrawal, S. 2004: T1 and M1 polymorphism in glutathione S-transferase gene and coronary artery disease in North Indian population Indian Journal of Medical Sciences 58(12): 520-526
Kowalski, M. 2001: Helicobacter pylori (H. pylori) infection in coronary artery disease: influence of H. pylori eradication on coronary artery lumen after percutaneous transluminal coronary angioplasty. the detection of H. pylori specific DNA in human coronary atherosclerotic plaque Journal of Physiology and Pharmacology An Official Journal of the Polish Physiological Society 52(1 Suppl 1): 3-31
Halim, E.F.A.E.; Reda, A.A.; Hendi, A.A.K.; Zaki, S.A.; Essa, E.S.; Khalifa, A.S. 2012: Apolipoprotein e gene variants as a risk factor for coronary artery disease in type 2 diabetic Egyptian patients Egyptian Journal of Immunology 19(1): 1-10
Varma, M.K.; Puri, G.D.; Chari, P.; Verma, J.S.; Kohli, K.K. 1996: Perioperative myocardial infarction in coronary artery disease patients and 'at-risk' for coronary artery disease patients undergoing non-cardiac surgery National Medical Journal of India 9(5): 214-217
Kovacs, I.B.; Jahangiri, M.; Ridler, C.D.; Görög, P.; Rees, G.M. 1998: Thrombogenic and atherogenic lipid modifications in plasma and patients with coronary artery disease and after coronary artery bypass surgery Rinsho Byori. Japanese Journal of Clinical Pathology 46(7): 656-662