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Results: 1 to 20 of 248

Similar articles for PubMed (Select 10706858)

1.

Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S.

Makris M, Leach M, Beauchamp NJ, Daly ME, Cooper PC, Hampton KK, Bayliss P, Peake IR, Miller GJ, Preston FE.

Blood. 2000 Mar 15;95(6):1935-41.

2.

The A20210 allele in the prothrombin gene enhances the risk of venous thrombosis in carriers of inherited protein S deficiency.

Castaman G, Tosetto A, Cappellari A, Ruggeri M, Rodeghiero F.

Blood Coagul Fibrinolysis. 2000 Jun;11(4):321-6.

PMID:
10847418
3.

Protein S type III deficiency is no risk factor for venous and arterial thromboembolism in 168 thrombophilic families: a retrospective study.

Libourel EJ, Bank I, Veeger NJ, Hamulyàk K, Middeldorp S, Prins MH, Büller HR, van der Meer J.

Blood Coagul Fibrinolysis. 2005 Mar;16(2):135-40.

PMID:
15741801
4.

The molecular mechanisms of inherited thrombophilia.

März W, Nauck M, Wieland H.

Z Kardiol. 2000 Jul;89(7):575-86. Review.

PMID:
10957782
5.
6.

A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.

Yin T, Takeshita S, Sato Y, Sakata T, Shin Y, Honda S, Kawasaki T, Tsuji H, Kojima T, Madoiwa S, Sakata Y, Murata M, Ikeda Y, Miyata T.

Thromb Haemost. 2007 Oct;98(4):783-9.

PMID:
17938802
7.

PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations.

Ten Kate MK, Platteel M, Mulder R, Terpstra P, Nicolaes GA, Reitsma PH, van der Steege G, van der Meer J.

Hum Mutat. 2008 Jul;29(7):939-47. doi: 10.1002/humu.20687.

PMID:
18435454
8.

Risk of venous thromboembolism in carriers of factor V Leiden with a concomitant inherited thrombophilic defect: a retrospective analysis.

Meinardi JR, Middeldorp S, de Kam PJ, Koopman MM, van Pampus EC, Hamulyák K, Prins MH, Büller HR, van der Meer J.

Blood Coagul Fibrinolysis. 2001 Dec;12(8):713-20.

PMID:
11734673
9.

Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S.

Zöller B, Berntsdotter A, García de Frutos P, Dahlbäck B.

Blood. 1995 Jun 15;85(12):3518-23.

10.

Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.

Tirado I, Mateo J, Soria JM, Oliver A, Borrell M, Coll I, Vallvé C, Souto JC, Martínez-Sánchez E, Fontcuberta J.

Haematologica. 2001 Nov;86(11):1200-8.

11.

High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin.

Brouwer JL, Lijfering WM, Ten Kate MK, Kluin-Nelemans HC, Veeger NJ, van der Meer J.

Thromb Haemost. 2009 Jan;101(1):93-9.

PMID:
19132194
12.

Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.

Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F.

Haematologica. 2000 Dec;85(12):1271-6.

13.

Co-segregation of the PROS1 locus and protein S deficiency in families having no detectable mutations in PROS1.

Lanke E, Johansson AM, Hillarp A, Lethagen S, Zöller B, Dahlbäck B, Halldén C.

J Thromb Haemost. 2004 Nov;2(11):1918-23.

PMID:
15550022
14.

One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.

Mizukami K, Nakabayashi T, Naitoh S, Takeda M, Tarumi T, Mizoguchi I, Ieko M, Koike T.

Am J Hematol. 2006 Oct;81(10):787-97.

PMID:
16868938
15.

Genetic risk factors for superficial vein thrombosis.

Martinelli I, Cattaneo M, Taioli E, De Stefano V, Chiusolo P, Mannucci PM.

Thromb Haemost. 1999 Oct;82(4):1215-7.

PMID:
10544900
16.

Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis.

Miyata T, Sato Y, Ishikawa J, Okada H, Takeshita S, Sakata T, Kokame K, Kimura R, Honda S, Kawasaki T, Suehisa E, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Ikeda Y.

Thromb Res. 2009 May;124(1):14-8. doi: 10.1016/j.thromres.2008.08.020. Epub 2008 Oct 26.

PMID:
18954896
17.

Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium.

Martinelli I, De Stefano V, Taioli E, Paciaroni K, Rossi E, Mannucci PM.

Thromb Haemost. 2002 May;87(5):791-5.

PMID:
12038778
18.

The pathogenesis of venous thromboembolism: evidence for multiple interrelated causes.

Brouwer JL, Veeger NJ, Kluin-Nelemans HC, van der Meer J.

Ann Intern Med. 2006 Dec 5;145(11):807-15.

PMID:
17146065
19.

Risk of recurrent venous thrombosis in children with combined prothrombotic risk factors.

Nowak-Göttl U, Junker R, Kreuz W, von Eckardstein A, Kosch A, Nohe N, Schobess R, Ehrenforth S; Childhood Thrombophilia Study Group.

Blood. 2001 Feb 15;97(4):858-62.

20.

[Genetic risk factors of venous thromboembolism].

Oner F, Kaya A, Doğan R, Numanoğlu N.

Tuberk Toraks. 2003;51(1):60-9. Review. Turkish.

PMID:
15100907
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