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A risk assessment model for the identification of hospitalized medical patients at risk for venous thromboembolism: the Padua Prediction Score

Journal of thrombosis and haemostasis, 2010-11, Vol.8 (11), p.2450-2457

2010

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Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma

Journal of thrombosis and haemostasis, 2010-02, Vol.8 (2), p.294-300

2010

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Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes

Thrombosis and haemostasis, 2014-03, Vol.111 (3), p.438

2014

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Sudden hearing loss followed by deep vein thrombosis and pulmonary embolism in a patient with factor V Leiden mutation

International journal of audiology, 2014-09, Vol.53 (9), p.625-628

2014

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Factor V Leiden pseudo-homozygotes have a more pronounced hypercoagulable state than factor V Leiden homozygotes

Journal of thrombosis and haemostasis, 2011-04, Vol.9 (4), p.864-867

2011

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Genetic modulation of the FVLeiden/normal FV ratio and risk of venous thrombosis in factor V Leiden heterozygotes

Journal of thrombosis and haemostasis, 2012-01, Vol.10 (1), p.73-80

2012

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Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia

Journal of thrombosis and haemostasis, 2007-05, Vol.5 (5), p.971-979

2007

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High vs. low doses of low‐molecular‐weight heparin for the treatment of superficial vein thrombosis of the legs: a double‐blind, randomized trial

Journal of thrombosis and haemostasis, 2005-06, Vol.3 (6), p.1152-1157

2005

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Risk for subsequent venous thromboembolic complications in carriers of the prothrombin or the factor V gene mutation with a first episode of deep-vein thrombosis

Blood, 2000-11, Vol.96 (10), p.3329-3333

2000

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The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A

Journal of thrombosis and haemostasis, 2008-03, Vol.6 (3), p.494-498

2008

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The risk of recurrent venous thromboembolism after discontinuing anticoagulation in patients with acute proximal deep vein thrombosis or pulmonary embolism. A prospective cohort study in 1,626 patients

Haematologica (Roma), 2007-02, Vol.92 (2), p.199-205

2007

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Duration of anticoagulation and risk of recurrent thromboembolism in carriers of factor V Leiden or prothrombin mutation

Journal of thrombosis and haemostasis, 2008-12, Vol.6 (12), p.2223-2224

2008

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Megakaryocytes endocytose and subsequently modify human factor V in vivo to form the entire pool of a unique platelet‐derived cofactor

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.450-456

2005

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D‐dimer as an adjunct to compression ultrasonography in patients with suspected recurrent deep vein thrombosis

Journal of thrombosis and haemostasis, 2007-05, Vol.5 (5), p.1076-1077

2007

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Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis

European journal of neurology, 2010-12, Vol.17 (12), p.1482-1485

2010

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Aspirin for Preventing the Recurrence of Venous Thromboembolism

The New England journal of medicine, 2012-05, Vol.366 (21), p.1959-1967

2012

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Immobilization resulting from chronic medical diseases: a new risk factor for recurrent venous thromboembolism in anticoagulated patients

Journal of thrombosis and haemostasis, 2007-08, Vol.5 (8), p.1786-1787

2007

Volltextzugriff (PDF)

The G20210A prothrombin variant and the risk of venous thromboembolism or fetal loss in pregnant women: a family study

Journal of thrombosis and haemostasis, 2007-11, Vol.5 (11), p.2193-2196

2007

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New anticoagulants for the treatment of venous thromboembolism

Minerva medica, 2013-04, Vol.104 (2), p.131

2013

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O007: Type of combined contraceptives and the risk of venous thromboembolism in antithrombin, protein C and protein S deficient women: a prospective cohort study

Thrombosis research, 2019-03, Vol.175, p.S3-S3

2019

Volltextzugriff (PDF)

PO-30 Inherited deficiency of antithrombin, protein C or protein S is associated with an increased risk of cancer at a younger age

Thrombosis research, 2021-04, Vol.200, p.S32-S33

2021

Volltextzugriff (PDF)

Factor V Leiden is associated with more distal location of deep vein thrombosis of the leg

Journal of thrombosis and haemostasis, 2008-03, Vol.6 (3), p.544-545

2008

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P.28 Factor V Leiden, PT-G20210A, MTHFR C677T mutations and the risk of implantation failure in women undergoing assisted reproductive procedures (IVF or ICSI)

Thrombosis research, 2011, Vol.127, p.S135-S136

2011

Volltextzugriff (PDF)

Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation

Journal of thrombosis and haemostasis, 2005-12, Vol.3 (12), p.2695-2702

2005

Volltextzugriff (PDF)

The G20210A prothrombin gene mutation: is there room for screening families?

Journal of thrombosis and haemostasis, 2004-08, Vol.2 (8), p.1487-1488

2004

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A risk assessment model for the identification of hospitalized medical patients at risk for venous thromboembolism: the Padua Prediction Score

Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma

Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes

Sudden hearing loss followed by deep vein thrombosis and pulmonary embolism in a patient with factor V Leiden mutation

Factor V Leiden pseudo-homozygotes have a more pronounced hypercoagulable state than factor V Leiden homozygotes

Genetic modulation of the FVLeiden/normal FV ratio and risk of venous thrombosis in factor V Leiden heterozygotes

Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia

High vs. low doses of low‐molecular‐weight heparin for the treatment of superficial vein thrombosis of the legs: a double‐blind, randomized trial

Risk for subsequent venous thromboembolic complications in carriers of the prothrombin or the factor V gene mutation with a first episode of deep-vein thrombosis

The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A

The risk of recurrent venous thromboembolism after discontinuing anticoagulation in patients with acute proximal deep vein thrombosis or pulmonary embolism. A prospective cohort study in 1,626 patients

Duration of anticoagulation and risk of recurrent thromboembolism in carriers of factor V Leiden or prothrombin mutation

Megakaryocytes endocytose and subsequently modify human factor V in vivo to form the entire pool of a unique platelet‐derived cofactor

D‐dimer as an adjunct to compression ultrasonography in patients with suspected recurrent deep vein thrombosis

Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis

Aspirin for Preventing the Recurrence of Venous Thromboembolism

Immobilization resulting from chronic medical diseases: a new risk factor for recurrent venous thromboembolism in anticoagulated patients

The G20210A prothrombin variant and the risk of venous thromboembolism or fetal loss in pregnant women: a family study

New anticoagulants for the treatment of venous thromboembolism

O007: Type of combined contraceptives and the risk of venous thromboembolism in antithrombin, protein C and protein S deficient women: a prospective cohort study

PO-30 Inherited deficiency of antithrombin, protein C or protein S is associated with an increased risk of cancer at a younger age

Factor V Leiden is associated with more distal location of deep vein thrombosis of the leg

P.28 Factor V Leiden, PT-G20210A, MTHFR C677T mutations and the risk of implantation failure in women undergoing assisted reproductive procedures (IVF or ICSI)

Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation

The G20210A prothrombin gene mutation: is there room for screening families?

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