Similar articles for PMID: 18524690

Year	Number of Results
2003	1
2005	2
2006	2
2007	9
2008	23
2009	25
2010	1
2011	3
2015	1
2016	1
2017	1
2018	1
2019	1
2024	0

1

Genetic risk factors in young patients with ischemic colitis.

Theodoropoulou A, Sfiridaki A, Oustamanolakis P, Vardas E, Livadiotaki A, Boumpaki A, Paspatis G, Koutroubakis IE. Theodoropoulou A, et al. Clin Gastroenterol Hepatol. 2008 Aug;6(8):907-11. doi: 10.1016/j.cgh.2008.03.010. Epub 2008 Jun 4. Clin Gastroenterol Hepatol. 2008. PMID: 18524690

2

The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolism.

Oguzulgen IK, Yilmaz E, Demirtas S, Erkekol FO, Ekim N, Demir N, Numanoglu N, Ozel D, Ulu A, Akar N. Oguzulgen IK, et al. Clin Appl Thromb Hemost. 2009 Feb;15(1):73-7. doi: 10.1177/1076029607305110. Epub 2007 Dec 26. Clin Appl Thromb Hemost. 2009. PMID: 18160588 Free article.

3

A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease.

Adamski MG, Turaj W, Slowik A, Wloch-Kopec D, Wolkow P, Szczudlik A. Adamski MG, et al. Acta Neurol Scand. 2009 Aug;120(2):94-100. doi: 10.1111/j.1600-0404.2008.01127.x. Epub 2008 Dec 22. Acta Neurol Scand. 2009. PMID: 19154538

4

The influence of established genetic variation in the haemostatic system on clinical restenosis after percutaneous coronary interventions.

Pons D, Monraats PS, de Maat MP, Pires NM, Quax PH, van Vlijmen BJ, Rosendaal FR, Zwinderman AH, Doevendans PA, Waltenberger J, de Winter RJ, Tio RA, Frants RR, van der Laarse A, van der Wall EE, Jukema JW. Pons D, et al. Thromb Haemost. 2007 Dec;98(6):1323-8. Thromb Haemost. 2007. PMID: 18064331

5

Genetic risk factors in patients with inflammatory bowel disease and vascular complications: case-control study.

Koutroubakis IE, Sfiridaki A, Tsiolakidou G, Theodoropoulou A, Livadiotaki A, Paspatis G, Kouroumalis EA. Koutroubakis IE, et al. Inflamm Bowel Dis. 2007 Apr;13(4):410-5. doi: 10.1002/ibd.20076. Inflamm Bowel Dis. 2007. PMID: 17206678

6

Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia.

Bedencic M, Bozic M, Peternel P, Stegnar M. Bedencic M, et al. Pathophysiol Haemost Thromb. 2008;36(2):58-63. doi: 10.1159/000173722. Epub 2009 Jan 5. Pathophysiol Haemost Thromb. 2008. PMID: 19127083

7

Inherited prothrombotic risk factors in children with stroke, transient ischemic attack, or migraine.

Herak DC, Antolic MR, Krleza JL, Pavic M, Dodig S, Duranovic V, Brkic AB, Zadro R. Herak DC, et al. Pediatrics. 2009 Apr;123(4):e653-60. doi: 10.1542/peds.2007-3737. Pediatrics. 2009. PMID: 19336355

8

The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis.

Ozmen F, Ozmen MM, Ozalp N, Akar N. Ozmen F, et al. Ulus Travma Acil Cerrahi Derg. 2009 Mar;15(2):113-9. Ulus Travma Acil Cerrahi Derg. 2009. PMID: 19353312 Free article.

9

Factor V HR2 haplotype: a risk factor for venous thromboembolism in individuals with absence of Factor V Leiden.

Otrock ZK, Taher AT, Shamseddeen WA, Zaatari G, Bazarbachi A, Mahfouz RA. Otrock ZK, et al. Ann Hematol. 2008 Dec;87(12):1013-6. doi: 10.1007/s00277-008-0543-3. Epub 2008 Jul 25. Ann Hematol. 2008. PMID: 18654780

10

Connection between genetically determined blood coagulation factors and haemorheology.

Pongrácz E, Andrikovics H, Bernát IS, Nagy Z. Pongrácz E, et al. Clin Hemorheol Microcirc. 2008;39(1-4):333-41. Clin Hemorheol Microcirc. 2008. PMID: 18503143

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