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Items: 1 to 20 of 87

1.
2.

Prevalence of 1691G>A FV mutation in Poland compared with that in other Central, Eastern and South-Eastern European countries.

Adler G, Clark JS, Loniewska B, Czerska E, Salkic NN, Ciechanowicz A.

Bosn J Basic Med Sci. 2012 May;12(2):82-7.

3.

The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individuals.

Ko YL, Hsu TS, Wu SM, Ko YS, Chang CJ, Wang SM, Chen WJ, Cheng NJ, Kuo CT, Chiang CW, Lee YS.

Hum Genet. 1996 Aug;98(2):176-7.

PMID:
8698336
4.

Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations.

Gregg JP, Yamane AJ, Grody WW.

Am J Med Genet. 1997 Dec 19;73(3):334-6.

PMID:
9415695
5.

Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria.

Renner W, Köppel H, Hoffmann C, Schallmoser K, Stanger O, Toplak H, Wascher TC, Pilger E.

Thromb Res. 2000 Jul 1;99(1):35-9.

PMID:
10904101
6.

Factor V Leiden is not common in patients diagnosed with primary pulmonary hypertension.

Elliott CG, Leppert MF, Alexander GJ, Ward K, Nelson L, Pietra GG.

Eur Respir J. 1998 Nov;12(5):1177-80.

7.

Coinheritance of factor V Leiden (F5 1691A) and prothrombin 20210 A (F2 20210A) in an Austrian family as cause for early onset of venous thromboembolism.

Brodmann M, Renner W, Stark G, Ramschak H, Seinost G, Pilger E.

Thromb Res. 2001 Mar 1;101(5):421-2. No abstract available.

PMID:
11421205
8.

Large-scale screening for factor V Leiden mutation in a north-eastern German population.

Schröder W, Koesling M, Wulff K, Wehnert M, Herrmann FH.

Haemostasis. 1996 Sep-Oct;26(5):233-6.

PMID:
8894653
9.

Population genetics of factor V Leiden in Europe.

Lucotte G, Mercier G.

Blood Cells Mol Dis. 2001 Mar-Apr;27(2):362-7.

PMID:
11259157
10.

World distribution of factor V Leiden.

Rees DC, Cox M, Clegg JB.

Lancet. 1995 Oct 28;346(8983):1133-4.

PMID:
7475606
11.

High incidence of factor V Leiden and prothrombin G20210A in healthy southern Italians.

Sottilotta G, Mammì C, Furlò G, Oriana V, Latella C, Trapani Lombardo V.

Clin Appl Thromb Hemost. 2009 May-Jun;15(3):356-9. doi: 10.1177/1076029607310218.

PMID:
19211580
12.

Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy.

Galanaud JP, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny JL, Mares P, Dauzat M, Quere I, Gris JC.

J Thromb Haemost. 2010 Apr;8(4):707-13. doi: 10.1111/j.1538-7836.2010.03770.x.

13.

Allelic polymorphism of F2, F5 and MTHFR genes in population of Ukraine.

Tatarskyy P, Kucherenko A, Livshits L.

Tsitol Genet. 2010 May-Jun;44(3):3-8.

PMID:
20608153
14.

Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.

Renner W, Köppel H, Brodmann M, Pabst E, Schallmoser K, Toplak H, Wascher TC, Pilger E.

Thromb Haemost. 2000 Jan;83(1):20-2.

PMID:
10669148
15.

A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.

Heit JA, Armasu SM, Asmann YW, Cunningham JM, Matsumoto ME, Petterson TM, De Andrade M.

J Thromb Haemost. 2012 Aug;10(8):1521-31. doi: 10.1111/j.1538-7836.2012.04810.x.

16.

Epidemiology of factor V Leiden: clinical implications.

De Stefano V, Chiusolo P, Paciaroni K, Leone G.

Semin Thromb Hemost. 1998;24(4):367-79. Review.

PMID:
9763354
17.

The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia.

Bôžiková A, Gabriková D, Sovičová A, Behulová R, Mačeková S, Boroňová I, Petrejčíková E, Soták M, Bernasovská J, Bernasovský I.

J Thromb Thrombolysis. 2012 Oct;34(3):406-9.

PMID:
22562116
18.
19.

The deltaccr5 mutation conferring protection against HIV-1 in Caucasian populations has a single and recent origin in Northeastern Europe.

Libert F, Cochaux P, Beckman G, Samson M, Aksenova M, Cao A, Czeizel A, Claustres M, de la Rúa C, Ferrari M, Ferrec C, Glover G, Grinde B, Güran S, Kucinskas V, Lavinha J, Mercier B, Ogur G, Peltonen L, Rosatelli C, Schwartz M, Spitsyn V, Timar L, Beckman L, Parmentier M, Vassart G.

Hum Mol Genet. 1998 Mar;7(3):399-406.

20.

A case control study of deep venous thrombosis in relation to factor V G1691A (Leiden) and A4070G (HR2 Haplotype) polymorphisms.

Bouaziz-Borgi L, Nguyen P, Hezard N, Musharrafieh U, Almawi WY, Mahjoub T.

Exp Mol Pathol. 2007 Dec;83(3):480-3.

PMID:
17555744
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