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Results: 1 to 20 of 135

Related Citations for PubMed (Select 21080081)

1.

Association of deep venous thrombosis with prothrombotic gene polymorphism identified in lung cancer cases.

Arslan S, Manduz S, Epöztürk K, Karahan O, Akkurt I.

Mol Biol Rep. 2011 Apr;38(4):2395-400. doi: 10.1007/s11033-010-0373-y. Epub 2010 Nov 16.

PMID:
21080081
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.

J Thromb Thrombolysis. 2005 Jun;19(3):189-96.

PMID:
16082606
3.

Analysis of thrombophilic genetic mutations in patients with Sheehan's syndrome: is thrombophilia responsible for the pathogenesis of Sheehan's syndrome?

Gokalp D, Tuzcu A, Bahceci M, Ayyildiz O, Yurt M, Celik Y, Alpagat G.

Pituitary. 2011 Jun;14(2):168-73. doi: 10.1007/s11102-010-0276-x.

PMID:
21107737
4.

A comprehensive analysis of 12 thrombophilic mutations and related parameters in patients with inflammatory bowel disease: data from Turkey.

Yilmaz S, Bayan K, Tüzün Y, Batun S, Altintaş A.

J Thromb Thrombolysis. 2006 Dec;22(3):205-12.

PMID:
17111197
5.

Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.

Xenophontos SL, Hadjivassiliou M, Ayrton N, Karagrigoriou A, Pantzaris M, Nicolaides AN, Cariolou MA.

Int Angiol. 2002 Dec;21(4):322-9.

PMID:
12518110
6.

Genetic and acquired prothrombotic risk factors and sudden hearing loss.

Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.

Laryngoscope. 2007 Mar;117(3):547-51.

PMID:
17334320
7.

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.

J Rheumatol. 2000 Dec;27(12):2849-54.

PMID:
11128675
8.

[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.

Vojnosanit Pregl. 2005 Mar;62(3):201-5. Serbian.

PMID:
15790048
10.

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.

Clin Appl Thromb Hemost. 2007 Oct;13(4):435-8.

PMID:
17911197
11.

Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.

González-Porras JR, García-Sanz R, Alberca I, López ML, Balanzategui A, Gutierrez O, Lozano F, San Miguel J.

Blood Coagul Fibrinolysis. 2006 Jan;17(1):23-8.

PMID:
16607075
12.

Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.

Lenicek Krleza J, Jakovljevic G, Bronic A, Coen Herak D, Bonevski A, Stepan-Giljevic J, Roic G.

Pathophysiol Haemost Thromb. 2010;37(1):24-9. doi: 10.1159/000319051. Epub 2010 Jul 20. Review.

PMID:
20664190
13.

Analysis of prothrombotic mutations and polymorphisms in children who developed thrombosis in the perioperative period of congenital cardiac surgery.

Ozbek N, Ataç FB, Yildirim SV, Verdi H, Yazici C, Yilmaz BT, Tokel NK.

Cardiol Young. 2005 Feb;15(1):19-25.

PMID:
15831156
14.

Detection of genomic polymorphisms associated with venous thrombosis using the invader biplex assay.

Patnaik M, Dlott JS, Fontaine RN, Subbiah MT, Hessner MJ, Joyner KA, Ledford MR, Lau EC, Moehlenkamp C, Amos J, Zhang B, Williams TM.

J Mol Diagn. 2004 May;6(2):137-44.

15.

A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.

Yenicesu GI, Cetin M, Ozdemir O, Cetin A, Ozen F, Yenicesu C, Yildiz C, Kocak N.

Am J Reprod Immunol. 2010 Feb;63(2):126-36. doi: 10.1111/j.1600-0897.2009.00770.x. Epub 2009 Nov 10.

PMID:
19906129
16.

Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: a family study.

Kosch A, Junker R, Kurnik K, Schobess R, Günther G, Koch H, Nowak-Göttl U.

Thromb Res. 2000 Sep 15;99(6):531-7.

PMID:
10974337
17.

Factor V Leiden and G20210A prothrombin mutation and the risk of subclavian vein thrombosis in patients with breast cancer and a central venous catheter.

Mandalà M, Curigliano G, Bucciarelli P, Ferretti G, Mannucci PM, Colleoni M, Ventura A, Peruzzotti G, Severi G, Pelicci PG, Biffi R, Orsi F, Cinieri S, Goldhirsch A.

Ann Oncol. 2004 Apr;15(4):590-3.

18.

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.

Gene. 2014 Feb 15;536(1):171-6. doi: 10.1016/j.gene.2013.11.019. Epub 2013 Dec 12.

PMID:
24334115
19.

Analysis of inherited thrombophilic mutations and natural anticoagulant deficiency in patients with idiopathic portal hypertension.

Bayan K, Tüzün Y, Yilmaz S, Canoruc N, Dursun M.

J Thromb Thrombolysis. 2009 Jul;28(1):57-62. doi: 10.1007/s11239-008-0244-8. Epub 2008 Aug 7.

PMID:
18685811
20.

Prevalence of factor V Leiden, FII G20210A, FXIII Val34Leu and MTHFR C677T polymorphisms in cancer patients with and without venous thrombosis.

Ramacciotti E, Wolosker N, Puech-Leao P, Zeratti EA, Gusson PR, del Giglio A, Franco RF.

Thromb Res. 2003 Feb 15;109(4):171-4.

PMID:
12757770
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