415 related articles for article (PubMed ID: 26187788)
1. Clinical Relevance of MTHFR, eNOS, ACE, and ApoE Gene Polymorphisms and Serum Vitamin Profile among Malay Patients with Ischemic Stroke.
Wei LK; Au A; Menon S; Gan SH; Griffiths LR
J Stroke Cerebrovasc Dis; 2015 Sep; 24(9):2017-25. PubMed ID: 26187788
[TBL] [Abstract][Full Text] [Related]
2. Polymorphisms of MTHFR, eNOS, ACE, AGT, ApoE, PON1, PDE4D, and Ischemic Stroke: Meta-Analysis.
Wei LK; Au A; Menon S; Griffiths LR; Kooi CW; Irene L; Zhao J; Lee C; Alekseevna AM; Hassan MRA; Aziz ZA
J Stroke Cerebrovasc Dis; 2017 Nov; 26(11):2482-2493. PubMed ID: 28760411
[TBL] [Abstract][Full Text] [Related]
3. Influence of combined methionine synthase (MTR 2756A > G) and methylenetetrahydrofolate reductase (MTHFR 677C > T) polymorphisms to plasma homocysteine levels in Korean patients with ischemic stroke.
Kim OJ; Hong SP; Ahn JY; Hong SH; Hwang TS; Kim SO; Yoo W; Oh D; Kim NK
Yonsei Med J; 2007 Apr; 48(2):201-9. PubMed ID: 17461517
[TBL] [Abstract][Full Text] [Related]
4. Prospective study of first stroke in relation to plasma homocysteine and MTHFR 677C>T and 1298A>C genotypes and haplotypes - evidence for an association with hemorrhagic stroke.
Hultdin J; Van Guelpen B; Winkvist A; Hallmans G; Weinehall L; Stegmayr B; Nilsson TK
Clin Chem Lab Med; 2011 Sep; 49(9):1555-62. PubMed ID: 21631392
[TBL] [Abstract][Full Text] [Related]
5. Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?
Djordjevic V; Stankovic M; Brankovic-Sreckovic V; Rakicevic L; Radojkovic D
J Child Neurol; 2009 Jul; 24(7):823-7. PubMed ID: 19372095
[TBL] [Abstract][Full Text] [Related]
6. Endothelial nitric oxide synthase -786T>C, but not 894G>T and 4a4b, polymorphism influences plasma homocysteine concentrations in persons with normal vitamin status.
Fatini C; Sofi F; Gori AM; Sticchi E; Marcucci R; Lenti M; Casini A; Surrenti C; Abbate R; Gensini GF
Clin Chem; 2005 Jul; 51(7):1159-64. PubMed ID: 15905312
[TBL] [Abstract][Full Text] [Related]
7. Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke.
Szolnoki Z; Havasi V; Bene J; Komlósi K; Szöke D; Somogyvári F; Kondacs A; Szabó M; Fodor L; Bodor A; Gáti I; Wittman I; Melegh B
Acta Neurol Scand; 2005 Jan; 111(1):29-33. PubMed ID: 15595935
[TBL] [Abstract][Full Text] [Related]
8. Endothelial nitric oxide synthase Glu298Asp, 4b/a, and -786T>C gene polymorphisms and the risk of ischemic stroke.
Saidi S; Mallat SG; Almawi WY; Mahjoub T
Acta Neurol Scand; 2010 Feb; 121(2):114-9. PubMed ID: 19804474
[TBL] [Abstract][Full Text] [Related]
9. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
Białecka M; Kurzawski M; Roszmann A; Robowski P; Sitek EJ; Honczarenko K; Gorzkowska A; Budrewicz S; Mak M; Jarosz M; Gołąb-Janowska M; Koziorowska-Gawron E; Droździk M; Sławek J
Pharmacogenet Genomics; 2012 Oct; 22(10):716-24. PubMed ID: 22890010
[TBL] [Abstract][Full Text] [Related]
10. Association between genetic polymorphisms and sites of cervicocerebral artery atherosclerosis.
Chutinet A; Suwanwela NC; Snabboon T; Chaisinanunkul N; Furie KL; Phanthumchinda K
J Stroke Cerebrovasc Dis; 2012 Jul; 21(5):379-85. PubMed ID: 21296594
[TBL] [Abstract][Full Text] [Related]
11. The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms in moyamoya disease patients.
Park YS; Jeon YJ; Kim HS; Han IB; Choi JU; Kim DS; Kim NK
Childs Nerv Syst; 2014 Oct; 30(10):1687-95. PubMed ID: 25098357
[TBL] [Abstract][Full Text] [Related]
12. Identification of genetic contribution to ischemic stroke by screening of single nucleotide polymorphisms in stroke patients by using a case control study design.
Kumar A; Sagar R; Kumar P; Sahu JK; Grover A; Srivastava AK; Vivekanandhan S; Prasad K
BMC Neurol; 2013 Oct; 13():136. PubMed ID: 24090469
[TBL] [Abstract][Full Text] [Related]
13. Signaling pathway genes for blood pressure, folate and cholesterol levels among hypertensives: an epistasis analysis.
Wei LK; Menon S; Griffiths LR; Gan SH
J Hum Hypertens; 2015 Feb; 29(2):99-104. PubMed ID: 25055800
[TBL] [Abstract][Full Text] [Related]
14. A potential epigenetic marker mediating serum folate and vitamin B12 levels contributes to the risk of ischemic stroke.
Wei LK; Sutherland H; Au A; Camilleri E; Haupt LM; Gan SH; Griffiths LR
Biomed Res Int; 2015; 2015():167976. PubMed ID: 25705649
[TBL] [Abstract][Full Text] [Related]
15. Methylenetetrahydrofolate reductase C677T polymorphism in Iraqi patients with ischemic stroke.
Al-Allawi NA; Avo AS; Jubrael JM
Neurol India; 2009; 57(5):631-5. PubMed ID: 19934565
[TBL] [Abstract][Full Text] [Related]
16. MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.
Jara-Prado A; Alonso ME; Martínez Ruano L; Guerrero Camacho J; Leyva A; López M; Gutierrez-Castrellon P; Arauz A
Int J Stroke; 2010 Apr; 5(2):80-5. PubMed ID: 20446941
[TBL] [Abstract][Full Text] [Related]
17. Dietary folate intake, MTHFR genetic polymorphisms, and the risk of endometrial cancer among Chinese women.
Xu WH; Shrubsole MJ; Xiang YB; Cai Q; Zhao GM; Ruan ZX; Cheng JR; Zheng W; Shu XO
Cancer Epidemiol Biomarkers Prev; 2007 Feb; 16(2):281-7. PubMed ID: 17301261
[TBL] [Abstract][Full Text] [Related]
18. The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring.
Vujkovic M; Steegers EA; van Meurs J; Yazdanpanah N; van Rooij IA; Uitterlinden AG; Steegers-Theunissen RP
Eur J Clin Nutr; 2010 Mar; 64(3):266-73. PubMed ID: 19935819
[TBL] [Abstract][Full Text] [Related]
19. 677C>T and 1298A>C polymorphisms of methylenetetrahydropholate reductase gene and biochemical parameters in Turkish population with spina bifida occulta.
Eser B; Cosar M; Eser O; Erdogan MO; Aslan A; Yildiz H; Boyaci G; Buyukbas S; Solak M
Turk Neurosurg; 2010 Jan; 20(1):9-15. PubMed ID: 20066615
[TBL] [Abstract][Full Text] [Related]
20. Rate of T alleles and TT genotype at MTHFR 677C->T locus or C alleles and CC genotype at MTHFR 1298A->C locus among healthy subjects in Turkey: impact on homocysteine and folic acid status and reference intervals.
Ozarda Y; Sucu DK; Hizli B; Aslan D
Cell Biochem Funct; 2009 Dec; 27(8):568-77. PubMed ID: 19764044
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]