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Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

Journal of thrombosis and haemostasis, 2021-08, Vol.19 (8), p.1959-1972

2021

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Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7

Medicina (Kaunas, Lithuania), 2020-09, Vol.56 (9), p.485

2020

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Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Human mutation, 2006-06, Vol.27 (6), p.600-600

2006

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Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement

Thrombosis and haemostasis, 2007-04, Vol.97 (4), p.678

2007

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Role of protein S deficiency in children with venous thromboembolism. An observational international cohort study

Thrombosis and haemostasis, 2015-02, Vol.113 (2), p.426

2015

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Clinical and laboratory characteristics of children with venous thromboembolism and protein C‐deficiency: an observational Israeli‐German cohort study

British journal of haematology, 2014-11, Vol.167 (3), p.385-393

2014

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Heparin-induced Thrombocytopenia Diagnosis: A Retrospective Study Comparing Heparin-induced Platelet Activation Test to 14C-serotonin Release Assay

TH open : companion journal to thrombosis and haemostasis, 2021-10, Vol.5 (4), p.e507-e512

2021

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Functional Flow Cytometric Assay for Reliable and Convenient Heparin-Induced Thrombocytopenia Diagnosis in Daily Practice

Biomedicines, 2021-03, Vol.9 (4), p.332

2021

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Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

Polskie archiwum medycyny wewne̦trznej, 2014-01, Vol.124 (1-2), p.75-76

2014

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Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes

Thrombosis and haemostasis, 1999-04, Vol.81 (4), p.506

1999

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The factor V gene A4070G mutation and the risk of venous thrombosis

Thrombosis and haemostasis, 1999-02, Vol.81 (2), p.193

1999

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Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

British journal of haematology, 2000-09, Vol.110 (3), p.731-734

2000

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Fetal Intracerebral Hemorrhage in Familial Thrombophilia

Pediatric neurology, 2009-10, Vol.41 (4), p.291-293

2009

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Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

British journal of haematology, 2002-04, Vol.117 (1), p.168-171

2002

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The -33T-->C polymorphism in intron 7 of the TFPI gene influences the risk of venous thromboembolism, independently of the factor V Leiden and prothrombin mutations

Thrombosis and haemostasis, 2002-08, Vol.88 (2), p.195

2002

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Mutations in promoter region of thrombomodulin and venous thromboembolic disease

Arteriosclerosis, thrombosis, and vascular biology, 1999-04, Vol.19 (4), p.1098

1999

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Venous thromboembolism associated with protein S deficiency due to [Formula omitted] mutation in PROS1 gene: a case report and a literature review

Journal of genetics, 2017-12, Vol.96 (6), p.1047

2017

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Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2718-2726

2010

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Prothrombotic mutations, hormone therapy, and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration

Circulation (New York, N.Y.), 2005-11, Vol.112 (22), p.3495-3500

2005

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Bilan de thrombophilie

Revue francophone des laboratoires, 2020-03, Vol.2020 (520), p.26-33

2020

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Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow)

Thrombosis and haemostasis, 2011-08, Vol.106 (2), p.379

2011

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Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Human mutation, 2006-11, Vol.27 (11), p.1160-1160

2006

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Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes

Thrombosis and haemostasis, 2005-01, Vol.93 (1), p.57

2005

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Differential effects of oral and transdermal estrogen/progesterone regimens on sensitivity to activated protein C among postmenopausal women: a randomized trial

Arteriosclerosis, thrombosis, and vascular biology, 2003-09, Vol.23 (9), p.1671

2003

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Effects of oral and transdermal estrogen/progesterone regimens on blood coagulation and fibrinolysis in postmenopausal women. A randomized controlled trial

Arteriosclerosis, thrombosis, and vascular biology, 1997-11, Vol.17 (11), p.3071

1997

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Heparin‐induced thrombocytopenia: Construction of a pretest diagnostic score derived from the analysis of a prospective multinational database, with internal validation

Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism: c.602-2delA, Splice Acceptor Site of Exon 7

Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement

Role of protein S deficiency in children with venous thromboembolism. An observational international cohort study

Clinical and laboratory characteristics of children with venous thromboembolism and protein C‐deficiency: an observational Israeli‐German cohort study

Heparin-induced Thrombocytopenia Diagnosis: A Retrospective Study Comparing Heparin-induced Platelet Activation Test to 14C-serotonin Release Assay

Functional Flow Cytometric Assay for Reliable and Convenient Heparin-Induced Thrombocytopenia Diagnosis in Daily Practice

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes

The factor V gene A4070G mutation and the risk of venous thrombosis

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

Fetal Intracerebral Hemorrhage in Familial Thrombophilia

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

The -33T-->C polymorphism in intron 7 of the TFPI gene influences the risk of venous thromboembolism, independently of the factor V Leiden and prothrombin mutations

Mutations in promoter region of thrombomodulin and venous thromboembolic disease

Venous thromboembolism associated with protein S deficiency due to [Formula omitted] mutation in PROS1 gene: a case report and a literature review

Protein S inherited qualitative deficiency: novel mutations and phenotypic influence

Prothrombotic mutations, hormone therapy, and venous thromboembolism among postmenopausal women : Impact of the route of estrogen administration

Bilan de thrombophilie

Arterial and venous thrombosis and prothrombotic fibrin clot phenotype in a Polish family with type 1 antithrombin deficiency (antithrombin Krakow)

Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene

Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes

Differential effects of oral and transdermal estrogen/progesterone regimens on sensitivity to activated protein C among postmenopausal women: a randomized trial

Effects of oral and transdermal estrogen/progesterone regimens on blood coagulation and fibrinolysis in postmenopausal women. A randomized controlled trial

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