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Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease

Thrombosis research, 2020-05, Vol.189, p.140-146

2020

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Activated factor VII–antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study

Journal of thrombosis and haemostasis, 2016-04, Vol.14 (4), p.655-666

2016

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Different lung responses to cigarette smoke in two strains of mice sensitive to oxidants

The European respiratory journal, 2005-01, Vol.25 (1), p.15-22

2005

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A Factor V Genetic Component Differing From Factor V R506Q Contributes to the Activated Protein C Resistance Phenotype

Blood, 1997-08, Vol.90 (4), p.1552-1557

1997

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C0398: Activated Factor VII-Antithrombin Complex Plasma Concentration is a Predictor of Total and Cardiovascular Mortality in Patients with Coronary Artery Disease and its Prognostic Significance is Improved by Using Factor VII Genotype-Specific Threshold Levels

Thrombosis research, 2014-05, Vol.133, p.S16-S16

2014

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Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-09, Vol.17 (5), p.822-824

2011

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Venous thromboembolism in young women. Role of thrombophilic mutations and oral contraceptive use

European heart journal, 2002-06, Vol.23 (12), p.984-990

2002

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Vitamin K‐induced modification of coagulation phenotype in VKORC1 homozygous deficiency

Journal of thrombosis and haemostasis, 2008-05, Vol.6 (5), p.797-803

2008

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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

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Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of congenital thrombophilia

Circulation (New York, N.Y.), 2003-07, Vol.108 (3), p.313-318

2003

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Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family

Blood, 2000-08, Vol.96 (4), p.1443-1448

2000

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Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma

Thrombosis and haemostasis, 1996-01, Vol.75 (1), p.45

1996

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C107 IMMUNITY, EXACERBATION AND IMMUNE CELL FUNCTION IN COPD: Severe Reduction Of Peripheral T Cells Does Not Afford Protection Toward Emphysema And Bronchial Remodelling Induced In Mice By Cigarette Smoke

American journal of respiratory and critical care medicine, 2016-01, Vol.193, p.1

2016

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Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?

Journal of thrombosis and haemostasis, 2005-02, Vol.3 (2), p.415-416

2005

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Different lung responses to cigarette smoke in two strains of mice sensitive to oxidants

The European respiratory journal, 2005-01, Vol.25 (1), p.15

2005

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OC 07.3 In vitro and ex vivo Rescue of a Nonsense Mutation (F5 p.Arg1161Ter) Responsible for Severe Coagulation Factor V Deficiency

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.100473, Article 100473

2023

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The factor V Glu1608Lys mutation is recurrent in familial thrombophilia

Journal of thrombosis and haemostasis, 2005-09, Vol.3 (9), p.2032-2038

2005

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Risks factors for highly unstable response to oral anticoagulation: a case‐control study

British journal of haematology, 2005-04, Vol.129 (1), p.72-78

2005

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A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population

Haematologica (Roma), 2001-06, Vol.86 (6), p.629

2001

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Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutation

Thrombosis and haemostasis, 2013-07, Vol.110 (1), p.31

2013

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A Novel Factor V Null Mutation Detected in a Thrombophilic Patient With Pseudo-Homozygous APC Resistance and in an Asymptomatic Unrelated Subject

Blood, 1998-08, Vol.92 (4), p.1463-1464

1998

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An underestimated combination of opposites resulting in enhanced thrombotic tendency

Blood, 2005-10, Vol.106 (7), p.2363-2365

2005

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A New Factor V Gene Polymorphism (His 1254 Arg) Present in Subjects of African Origin Mimics the R2 Polymorphism (His 1299 Arg)

Blood, 1998-01, Vol.91 (1), p.364-365

1998

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New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians

Thrombosis and haemostasis, 1997-09, Vol.78 (3), p.1037

1997

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A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V‐related disorders

British journal of haematology, 2001-09, Vol.114 (4), p.868-870

2001

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Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease

Activated factor VII–antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study

Different lung responses to cigarette smoke in two strains of mice sensitive to oxidants

A Factor V Genetic Component Differing From Factor V R506Q Contributes to the Activated Protein C Resistance Phenotype

C0398: Activated Factor VII-Antithrombin Complex Plasma Concentration is a Predictor of Total and Cardiovascular Mortality in Patients with Coronary Artery Disease and its Prognostic Significance is Improved by Using Factor VII Genotype-Specific Threshold Levels

Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors

Venous thromboembolism in young women. Role of thrombophilic mutations and oral contraceptive use

Vitamin K‐induced modification of coagulation phenotype in VKORC1 homozygous deficiency

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

Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of congenital thrombophilia

Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family

Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma

C107 IMMUNITY, EXACERBATION AND IMMUNE CELL FUNCTION IN COPD: Severe Reduction Of Peripheral T Cells Does Not Afford Protection Toward Emphysema And Bronchial Remodelling Induced In Mice By Cigarette Smoke

Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels?

Different lung responses to cigarette smoke in two strains of mice sensitive to oxidants

OC 07.3 In vitro and ex vivo Rescue of a Nonsense Mutation (F5 p.Arg1161Ter) Responsible for Severe Coagulation Factor V Deficiency

The factor V Glu1608Lys mutation is recurrent in familial thrombophilia

Risks factors for highly unstable response to oral anticoagulation: a case‐control study

A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population

Molecular basis of coagulation factor V deficiency caused by the R1698W inter-domain mutation

A Novel Factor V Null Mutation Detected in a Thrombophilic Patient With Pseudo-Homozygous APC Resistance and in an Asymptomatic Unrelated Subject

An underestimated combination of opposites resulting in enhanced thrombotic tendency

A New Factor V Gene Polymorphism (His 1254 Arg) Present in Subjects of African Origin Mimics the R2 Polymorphism (His 1299 Arg)

New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians

A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V‐related disorders

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