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    Results: 1 to 20 of 301

    1.

    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 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Oral contraceptives and the absolute risk of venous thromboembolism in women with single or multiple thrombophilic defects: results from a retrospective family cohort study.

    van Vlijmen EF, Brouwer JL, Veeger NJ, Eskes TK, de Graeff PA, van der Meer J.

    Arch Intern Med. 2007 Feb 12;167(3):282-9.PMID: 17296885 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    High risk of pregnancy-related venous thromboembolism in women with multiple thrombophilic defects.

    Folkeringa N, Brouwer JL, Korteweg FJ, Veeger NJ, Erwich JJ, van der Meer J.

    Br J Haematol. 2007 Jul;138(1):110-6.PMID: 17555454 [PubMed - indexed for MEDLINE]Related articles

    4.

    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 [PubMed - indexed for MEDLINE]Related articles

    5.

    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 [PubMed - indexed for MEDLINE]Related articles

    6.

    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 [PubMed - indexed for MEDLINE]Related articles

    7.

    Risk of venous thromboembolism and clinical manifestations in carriers of antithrombin, protein C, protein S deficiency, or activated protein C resistance: a multicenter collaborative family study.

    Bucciarelli P, Rosendaal FR, Tripodi A, Mannucci PM, De Stefano V, Palareti G, Finazzi G, Baudo F, Quintavalla R.

    Arterioscler Thromb Vasc Biol. 1999 Apr;19(4):1026-33.PMID: 10195932 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    The incidence of venous thromboembolism in carriers of antithrombin, protein C or protein S deficiency associated with the HR2 haplotype of factor V: a family cohort study.

    Tormene D, Fortuna S, Tognin G, Gavasso S, Pagnan A, Prandoni P, Simioni P.

    J Thromb Haemost. 2005 Jul;3(7):1414-20.PMID: 15978097 [PubMed - indexed for MEDLINE]Related articles

    9.

    Incidence of venous thromboembolism in families with inherited thrombophilia.

    Simioni P, Sanson BJ, Prandoni P, Tormene D, Friederich PW, Girolami B, Gavasso S, Huisman MV, Büller HR, Wouter ten Cate J, Girolami A, Prins MH.

    Thromb Haemost. 1999 Feb;81(2):198-202.PMID: 10063991 [PubMed - indexed for MEDLINE]Related articles

    10.

    Risk of venous thromboembolism in relatives of symptomatic probands with thrombophilia: a systematic review.

    Langlois NJ, Wells PS.

    Thromb Haemost. 2003 Jul;90(1):17-26. Review.PMID: 12876621 [PubMed - indexed for MEDLINE]Related articles

    11.

    Hereditary deficiency of protein C or protein S confers increased risk of arterial thromboembolic events at a young age: results from a large family cohort study.

    Mahmoodi BK, Brouwer JL, Veeger NJ, van der Meer J.

    Circulation. 2008 Oct 14;118(16):1659-67. Epub 2008 Sep 29.PMID: 18824642 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives.

    Lijfering WM, Brouwer JL, Veeger NJ, Bank I, Coppens M, Middeldorp S, Hamulyák K, Prins MH, Büller HR, van der Meer J.

    Blood. 2009 May 21;113(21):5314-22. Epub 2009 Jan 12.PMID: 19139080 [PubMed - indexed for MEDLINE]Related articles

    13.

    Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test-based classification.

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

    Br J Haematol. 2005 Mar;128(5):703-10.PMID: 15725093 [PubMed - indexed for MEDLINE]Related articles

    14.

    The incidence of venous thromboembolism in asymptomatic carriers of a deficiency of antithrombin, protein C, or protein S: a prospective cohort study.

    Sanson BJ, Simioni P, Tormene D, Moia M, Friederich PW, Huisman MV, Prandoni P, Bura A, Rejto L, Wells P, Mannucci PM, Girolami A, Büller HR, Prins MH.

    Blood. 1999 Dec 1;94(11):3702-6.PMID: 10572082 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    The contribution of inherited and acquired thrombophilic defects, alone or combined with antiphospholipid antibodies, to venous and arterial thromboembolism in patients with systemic lupus erythematosus.

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

    Blood. 2004 Jul 1;104(1):143-8. Epub 2004 Mar 16.PMID: 15026314 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    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.PMID: 11159508 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Screening for inherited thrombophilia: indications and therapeutic implications.

    De Stefano V, Rossi E, Paciaroni K, Leone G.

    Haematologica. 2002 Oct;87(10):1095-108. Review.PMID: 12368166 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Gene-gene and gene-environment interactions determine risk of thrombosis in families with inherited antithrombin deficiency.

    van Boven HH, Vandenbroucke JP, Briët E, Rosendaal FR.

    Blood. 1999 Oct 15;94(8):2590-4.PMID: 10515862 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Elevated levels of FVIII:C within families are associated with an increased risk for venous and arterial thrombosis.

    Bank I, Libourel EJ, Middeldorp S, Hamulyák K, van Pampus EC, Koopman MM, Prins MH, van der Meer J, Büller HR.

    J Thromb Haemost. 2005 Jan;3(1):79-84.PMID: 15634269 [PubMed - indexed for MEDLINE]Related articles

    20.

    Prothrombin 20210A mutation: a mild risk factor for venous thromboembolism but not for arterial thrombotic disease and pregnancy-related complications in a family study.

    Bank I, Libourel EJ, Middeldorp S, Van Pampus EC, Koopman MM, Hamulyák K, Prins MH, Van Der Meer J, Büller HR.

    Arch Intern Med. 2004 Sep 27;164(17):1932-7.PMID: 15451770 [PubMed - indexed for MEDLINE]Related articlesFree article

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