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118 related items for PubMed ID: 38526965
21. Polymorphism in methylenetetrahydrofolate reductase gene: its impact on plasma homocysteine levels and carotid atherosclerosis in ESRD patients receiving hemodialysis. Lim PS, Hung WR, Wei YH. Nephron; 2001 Mar; 87(3):249-56. PubMed ID: 11287760 [Abstract] [Full Text] [Related]
22. Impact of plasma homocysteine and prothrombin G20210 A on primary antiphospholipid syndrome. Ames PR, Margaglione M, Tommasino C, Bossone A, Iannaccone L, Brancaccio V. Blood Coagul Fibrinolysis; 2001 Dec; 12(8):699-704. PubMed ID: 11734671 [Abstract] [Full Text] [Related]
23. Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis. Amitrano L, Brancaccio V, Guardascione MA, Margaglione M, Iannaccone L, D'Andrea G, Marmo R, Ames PR, Balzano A. Hepatology; 2000 Feb; 31(2):345-8. PubMed ID: 10655256 [Abstract] [Full Text] [Related]
24. Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease. Domagala TB, Adamek L, Nizankowska E, Sanak M, Szczeklik A. Blood Coagul Fibrinolysis; 2002 Jul; 13(5):423-31. PubMed ID: 12138370 [Abstract] [Full Text] [Related]
25. Gene--nutrition interactions in coronary artery disease: correlation between the MTHFR C677T polymorphism and folate and homocysteine status in a Korean population. Huh HJ, Chi HS, Shim EH, Jang S, Park CJ. Thromb Res; 2006 Jul; 117(5):501-6. PubMed ID: 15935452 [Abstract] [Full Text] [Related]
26. Methylenetetrahydrofolate reductase gene C677T mutation and plasma homocysteine level in Behçet's disease. Canataroglu A, Tanriverdi K, Inal T, Seydaoglu G, Arslan D, Ozbek S, Baslamisli F. Rheumatol Int; 2003 Sep; 23(5):236-40. PubMed ID: 14504916 [Abstract] [Full Text] [Related]
27. Interactions between genetic variants involved in the folate metabolic pathway and serum lipid, homocysteine levels on the risk of recurrent spontaneous abortion. Lin Z, Li Q, Sun Y, Huang J, Wang W, Fu J, Xu J, Zeng D. Lipids Health Dis; 2019 Jun 15; 18(1):143. PubMed ID: 31200713 [Abstract] [Full Text] [Related]
28. Clinical significance of determining plasma homocysteine: case-control study on arterial and venous thrombotic patients. Vuckovic BA, Cabarkapa VS, Ilic TA, Salatic IR, Lozanov-Crvenkovic ZS, Mitic GP. Croat Med J; 2013 Oct 28; 54(5):480-8. PubMed ID: 24170727 [Abstract] [Full Text] [Related]
29. Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis. Khandanpour N, Willis G, Meyer FJ, Armon MP, Loke YK, Wright AJ, Finglas PM, Jennings BA. J Vasc Surg; 2009 Mar 28; 49(3):711-8. PubMed ID: 19157768 [Abstract] [Full Text] [Related]
30. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil. Siqueira ER, Oliveira CP, Muniz MT, Silva F, Pereira LM, Carrilho FJ. Nutr J; 2011 Aug 19; 10():86. PubMed ID: 21854603 [Abstract] [Full Text] [Related]
31. [Association between gene polymorphisms of methylenetetrahydrofolate reductase and plasma homocysteine in Uygur patients with venous thromboembolism]. Abudureheman K, Mahemuti A, Xia YN, Hu XM. Zhonghua Xin Xue Guan Bing Za Zhi; 2012 Dec 19; 40(12):1030-6. PubMed ID: 23363719 [Abstract] [Full Text] [Related]
32. The impact of MTHFR 677 C/T genotypes on folate status markers: a meta-analysis of folic acid intervention studies. Colson NJ, Naug HL, Nikbakht E, Zhang P, McCormack J. Eur J Nutr; 2017 Feb 19; 56(1):247-260. PubMed ID: 26497154 [Abstract] [Full Text] [Related]
34. Possible Association Between the Methylenetetrahydrofolate Reductase Gene C677T Polymorphism and Preexisting Portal Vein Thrombosis in Liver Transplant Recipients. Kamei H, Nakamura T, Nagai S, Ishigami M, Hamajima N. Exp Clin Transplant; 2016 Jun 19; 14(3):313-6. PubMed ID: 27221722 [Abstract] [Full Text] [Related]
35. Association of a common polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with bone phenotypes depends on plasma folate status. McLean RR, Karasik D, Selhub J, Tucker KL, Ordovas JM, Russo GT, Cupples LA, Jacques PF, Kiel DP. J Bone Miner Res; 2004 Mar 19; 19(3):410-8. PubMed ID: 15040829 [Abstract] [Full Text] [Related]
36. The relationship between riboflavin and plasma total homocysteine in the Framingham Offspring cohort is influenced by folate status and the C677T transition in the methylenetetrahydrofolate reductase gene. Jacques PF, Kalmbach R, Bagley PJ, Russo GT, Rogers G, Wilson PW, Rosenberg IH, Selhub J. J Nutr; 2002 Feb 19; 132(2):283-8. PubMed ID: 11823591 [Abstract] [Full Text] [Related]
37. 5,10-Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms: genotype frequency and association with homocysteine and folate levels in middle-southern Italian adults. Zappacosta B, Graziano M, Persichilli S, Di Castelnuovo A, Mastroiacovo P, Iacoviello L. Cell Biochem Funct; 2014 Jan 19; 32(1):1-4. PubMed ID: 24277487 [Abstract] [Full Text] [Related]
38. Heterozygous prothrombin 20210G/A mutation, associated with hyperhomocysteinemia, and homozygous methylenetetrahydrofolate reductase 677C/T mutation, in a patient with portal and mesenteric venous thrombosis. Elhajj II, Salem ZM, Birjawi GA, Taher AT, Soweid AM. Hematol J; 2004 Jan 19; 5(6):540-2. PubMed ID: 15570301 [Abstract] [Full Text] [Related]
39. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease. Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W. Kardiol Pol; 2003 Jul 19; 59(7):17-26; discussion 26. PubMed ID: 14560345 [Abstract] [Full Text] [Related]
40. Correlation between C677T MTHFR gene polymorphism, plasma homocysteine levels and the incidence of CAD. Nakai K, Itoh C, Nakai K, Habano W, Gurwitz D. Am J Cardiovasc Drugs; 2001 Jul 19; 1(5):353-61. PubMed ID: 14728017 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]