Similar articles for PMID: 12570104

Year	Number of Results
1996	1
1998	10
1999	25
2000	27
2001	19
2002	18
2003	21
2004	10
2005	9
2006	15
2007	10
2008	12
2009	15
2010	12
2011	10
2012	9
2013	7
2014	9
2015	11
2016	8
2017	8
2018	8
2019	8
2020	11
2021	11
2022	10
2023	5
2024	1

1

Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis.

Nizankowska-Mogilnicka E, Adamek L, Grzanka P, Domagala TB, Sanak M, Krzanowski M, Szczeklik A. Nizankowska-Mogilnicka E, et al. Eur Respir J. 2003 Jan;21(1):25-30. doi: 10.1183/09031936.03.00034302. Eur Respir J. 2003. PMID: 12570104 Free article.

2

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.

Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, Nabulsi M, Finan RR, Irani-Hakime N. Almawi WY, et al. J Thromb Thrombolysis. 2005 Jun;19(3):189-96. doi: 10.1007/s11239-005-1313-x. J Thromb Thrombolysis. 2005. PMID: 16082606

3

Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.

Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I. Toydemir PB, et al. J Rheumatol. 2000 Dec;27(12):2849-54. J Rheumatol. 2000. PMID: 11128675

4

[Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium].

Dordević V, Rakićević L, Spasić M, Miković D, Kovać M, Radojković D. Dordević V, et al. Vojnosanit Pregl. 2005 Mar;62(3):201-5. doi: 10.2298/vsp0503201d. Vojnosanit Pregl. 2005. PMID: 15790048 Serbian.

5

Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations.

Grandone E, Margaglione M, Colaizzo D, D'Andrea G, Cappucci G, Brancaccio V, Di Minno G. Grandone E, et al. Am J Obstet Gynecol. 1998 Nov;179(5):1324-8. doi: 10.1016/s0002-9378(98)70155-3. Am J Obstet Gynecol. 1998. PMID: 9822524

6

Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.

Dölek B, Eraslan S, Eroğlu S, Kesim BE, Ulutin T, Yalçiner A, Laleli YR, Gözükirmizi N. Dölek B, et al. Clin Appl Thromb Hemost. 2007 Oct;13(4):435-8. doi: 10.1177/1076029607303341. Clin Appl Thromb Hemost. 2007. PMID: 17911197 Free article.

7

Genetic mutations in Turkish population with pulmonary embolism and deep venous thrombosis.

Kupeli E, Verdi H, Simsek A, Atac FB, Eyuboglu FO. Kupeli E, et al. Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):E87-94. doi: 10.1177/1076029610385224. Epub 2010 Nov 15. Clin Appl Thromb Hemost. 2011. PMID: 21078611 Free article.

8

The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels.

Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L. Cattaneo M, et al. Thromb Res. 1999 Jan 1;93(1):1-8. doi: 10.1016/s0049-3848(98)00136-4. Thromb Res. 1999. PMID: 10065893

9

Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence.

Simsek E, Yesilyurt A, Pinarli F, Eyerci N, Ulus AT. Simsek E, et al. Gene. 2014 Feb 15;536(1):171-6. doi: 10.1016/j.gene.2013.11.019. Epub 2013 Dec 12. Gene. 2014. PMID: 24334115

10

Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population.

Lu Y, Zhao Y, Liu G, Wang X, Liu Z, Chen B, Hui R. Lu Y, et al. Thromb Res. 2002 Apr 1;106(1):7-12. doi: 10.1016/s0049-3848(02)00064-6. Thromb Res. 2002. PMID: 12165282

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