113 related articles for article (PubMed ID: 20586826)
21. The risk for thromboembolic disease in lupus anticoagulant patients due to pathways involving P-selectin and CD154.
Bugert P; Pabinger I; Stamer K; Vormittag R; Skeate RC; Wahi MM; Panzer S
Thromb Haemost; 2007 Apr; 97(4):573-80. PubMed ID: 17393020
[TBL] [Abstract][Full Text] [Related]
22. Possible gender-dependent association of vascular endothelial growth factor (VEGF) gene and ALS.
Fernández-Santiago R; Sharma M; Mueller JC; Gohlke H; Illig T; Anneser J; Münch C; Ludolph A; Kamm C; Gasser T
Neurology; 2006 Jun; 66(12):1929-31. PubMed ID: 16801663
[TBL] [Abstract][Full Text] [Related]
23. [Study on linkage between polymorphism of interleukin 6 gene -572C/G and susceptibility to myocardial infarction].
Fu HX; Zhang JY; Li GS; Li Y; Xu JL; Zhao ZN
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):245-9. PubMed ID: 16767656
[TBL] [Abstract][Full Text] [Related]
24. Assessment of genetic risk for myocardial infarction.
Yamada Y; Matsuo H; Segawa T; Watanabe S; Kato K; Hibino T; Yokoi K; Ichihara S; Metoki N; Yoshida H; Satoh K; Nozawa Y
Thromb Haemost; 2006 Aug; 96(2):220-7. PubMed ID: 16894468
[TBL] [Abstract][Full Text] [Related]
25. The myeloperoxidase gene and its influence on myocardial infarction in a Swedish population: protective role of the -129A allele in women.
Zotova E; Lyrenäs L; de Faire U; Morgenstern R; Gigante B; Bennet AM
Coron Artery Dis; 2009 Aug; 20(5):322-6. PubMed ID: 19543083
[TBL] [Abstract][Full Text] [Related]
26. No association of common VCP variants with sporadic frontotemporal dementia.
Schumacher A; Friedrich P; Diehl J; Ibach B; Schoepfer-Wendels A; Mueller JC; Konta L; Laws SM; Kurz A; Foerstl H; Riemenschneider M
Neurobiol Aging; 2009 Feb; 30(2):333-5. PubMed ID: 17618707
[TBL] [Abstract][Full Text] [Related]
27. Polymorphisms in the paraoxonase and endothelial nitric oxide synthase genes and the risk of early-onset myocardial infarction.
Morray B; Goldenberg I; Moss AJ; Zareba W; Ryan D; McNitt S; Eberly SW; Glazko G; Mathew J
Am J Cardiol; 2007 Apr; 99(8):1100-5. PubMed ID: 17437735
[TBL] [Abstract][Full Text] [Related]
28. Re: Beta1 and beta2-adrenergic receptor polymorphisms and idiopathic ventricular arrhythmias.
Sauer M
J Cardiovasc Electrophysiol; 2008 Dec; 19(12):E55; author reply E56. PubMed ID: 19120684
[No Abstract] [Full Text] [Related]
29. A promoter polymorphism of the alpha 8 integrin gene and the progression of autosomal-dominant polycystic kidney disease.
Zeltner R; Hilgers KF; Schmieder RE; Porst M; Schulze BD; Hartner A
Nephron Clin Pract; 2008; 108(3):c169-75. PubMed ID: 18277079
[TBL] [Abstract][Full Text] [Related]
30. Progesterone receptor +331G/A polymorphism in endometriosis and deep-infiltrating endometriosis.
Gentilini D; Vigano P; Carmignani L; Spinelli M; Busacca M; Di Blasio AM
Fertil Steril; 2008 Oct; 90(4):1243-5. PubMed ID: 18281038
[TBL] [Abstract][Full Text] [Related]
31. The G1246A polymorphism in the hypocretin receptor 2 gene is not associated with treatment response in cluster headache.
Schürks M; Kurth T; Geissler I; Tessmann G; Diener HC; Rosskopf D
Cephalalgia; 2007 Apr; 27(4):363-7. PubMed ID: 17376114
[TBL] [Abstract][Full Text] [Related]
32. Association study of the paraoxonase 1 gene with the risk of developing Alzheimer's disease.
Chapuis J; Boscher M; Bensemain F; Cottel D; Amouyel P; Lambert JC
Neurobiol Aging; 2009 Jan; 30(1):152-6. PubMed ID: 17624629
[TBL] [Abstract][Full Text] [Related]
33. Association of rs2781666 G/T polymorphism of arginase I gene with myocardial infarction in Tunisian male population.
Sediri Y; Kallel A; Ben Ali S; Omar S; Mourali MS; Elasmi M; Taieb SH; Sanhaji H; Feki M; Mechmeche R; Jemaa R; Kaabachi N
Clin Biochem; 2010 Jan; 43(1-2):106-9. PubMed ID: 19896478
[TBL] [Abstract][Full Text] [Related]
34. Association between PPARalpha gene polymorphisms and myocardial infarction.
Reinhard W; Stark K; Sedlacek K; Fischer M; Baessler A; Neureuther K; Weber S; Kaess B; Wiedmann S; Mitsching S; Lieb W; Erdmann J; Meisinger C; Doering A; Tolle R; Jeron A; Riegger G; Hengstenberg C
Clin Sci (Lond); 2008 Nov; 115(10):301-8. PubMed ID: 18336366
[TBL] [Abstract][Full Text] [Related]
35. Genetic polymorphisms contribute to acute kidney injury after coronary artery bypass grafting.
Isbir SC; Tekeli A; Ergen A; Yilmaz H; Ak K; Civelek A; Zeybek U; Arsan S
Heart Surg Forum; 2007; 10(6):E439-44. PubMed ID: 17921131
[TBL] [Abstract][Full Text] [Related]
36. Could sustained monomorphic ventricular tachycardia in the early phase of a prime acute myocardial infarction affect patient outcome?
Hatzinikolaou-Kotsakou E; Tziakas D; Hotidis A; Stakos D; Floros D; Mavridis A; Papanas N; Chalikias G; Maltezos E; Hatseras DI
J Electrocardiol; 2007 Jan; 40(1):72-7. PubMed ID: 17070829
[TBL] [Abstract][Full Text] [Related]
37. Genetic variation in the KCNMA1 potassium channel alpha subunit as risk factor for severe essential hypertension and myocardial infarction.
Tomás M; Vázquez E; Fernández-Fernández JM; Subirana I; Plata C; Heras M; Vila J; Marrugat J; Valverde MA; Sentí M
J Hypertens; 2008 Nov; 26(11):2147-53. PubMed ID: 18854754
[TBL] [Abstract][Full Text] [Related]
38. Current evidence for a modulation of nociception by human genetic polymorphisms.
Lötsch J; Geisslinger G
Pain; 2007 Nov; 132(1-2):18-22. PubMed ID: 17706868
[No Abstract] [Full Text] [Related]
39. L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms.
Yokoyama K; Urashima M; Ohkido I; Kono T; Yoshida T; Muramatsu M; Niu T; Hosoya T
Nephron Clin Pract; 2010; 115(4):c237-43. PubMed ID: 20424473
[TBL] [Abstract][Full Text] [Related]
40. A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.
Gemmati D; Serino ML; Ongaro A; Tognazzo S; Moratelli S; Resca R; Moretti M; Scapoli GL
Am J Hematol; 2001 Jul; 67(3):183-8. PubMed ID: 11391716
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]