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Concomitant infusion of low doses of rFVIIa and FEIBA in haemophilia patients with inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-07, Vol.15 (4), p.904-910

2009

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Geographic distribution of the 20210 G to A prothrombin variant

Thrombosis and haemostasis, 1998-04, Vol.79 (4), p.706-708

1998

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Point mutations regarded as missense mutations cause splicing defects in the factor XI gene

Journal of thrombosis and haemostasis, 2011-10, Vol.9 (10), p.1977-1984

2011

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Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors - a thrombin generation-guided pilot study

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-09, Vol.19 (5), p.782-789

2013

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Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews

Journal of thrombosis and haemostasis, 2013-04, Vol.11 (4), p.724-730

2013

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Effects of factor VIII inhibitor bypassing activity (FEIBA), recombinant factor VIIa or both on thrombin generation in normal and haemophilia A plasma

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-07, Vol.14 (4), p.782-786

2008

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Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI

Journal of thrombosis and haemostasis, 2009-06, Vol.7 (6), p.970-975

2009

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Prerequisites for recombinant factor VIIa‐induced thrombin generation in plasmas deficient in factors VIII, IX or XI

Journal of thrombosis and haemostasis, 2006-01, Vol.4 (1), p.192-200

2006

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Inherited factor XI deficiency confers no protection against acute myocardial infarction

Journal of thrombosis and haemostasis, 2003-04, Vol.1 (4), p.658-661

2003

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Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Journal of thrombosis and haemostasis, 2004-10, Vol.2 (10), p.1774-1781

2004

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Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-05, Vol.15 (3), p.774-778

2009

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A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency

Journal of thrombosis and haemostasis, 2004-06, Vol.2 (6), p.918-924

2004

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The role of factor XI in thrombin generation induced by low concentrations of tissue factor

Thrombosis and haemostasis, 2001-06, Vol.85 (6), p.1060-1065

2001

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Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis

Thrombosis and haemostasis, 2011-02, Vol.105 (2), p.269-273

2011

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Seven novel mutations in the factor XIII A‐subunit gene causing hereditary factor XIII deficiency in 10 unrelated families

Journal of thrombosis and haemostasis, 2004-10, Vol.2 (10), p.1790-1797

2004

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Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphism

Stroke (1970), 2001-12, Vol.32 (12), p.2753-2758

2001

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Do platelets synthesize factor XI?

Journal of thrombosis and haemostasis, 2004-10, Vol.2 (10), p.1709-1712

2004

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Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI–Glu555): a cross‐reactive material positive variant defective in factor IX activation

Journal of thrombosis and haemostasis, 2004-10, Vol.2 (10), p.1782-1789

2004

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The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques

Journal of thrombosis and haemostasis, 2004-02, Vol.2 (2), p.361-362

2004

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A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor

Thrombosis and haemostasis, 2011-04, Vol.105 (4), p.688-695

2011

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The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans

American journal of human genetics, 2002-03, Vol.70 (3), p.758-762

2002

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Thrombophilia as a multigenic disorder

Thrombosis and haemostasis, 1997-07, Vol.78 (1), p.297-301

1997

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The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel

Thrombosis and haemostasis, 1989-02, Vol.61 (1), p.50-54

1989

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Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

The Journal of biological chemistry, 2001-10, Vol.276 (40), p.36923-36930

2001

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Clinical significance of antibodies to bovine and human thrombin and factor V after surgical use of bovine thrombin

American journal of clinical pathology, 1992, Vol.97 (1), p.84-91

1992

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Concomitant infusion of low doses of rFVIIa and FEIBA in haemophilia patients with inhibitors

Geographic distribution of the 20210 G to A prothrombin variant

Point mutations regarded as missense mutations cause splicing defects in the factor XI gene

Combined administration of FVIII and rFVIIa improves haemostasis in haemophilia A patients with high-responding inhibitors - a thrombin generation-guided pilot study

Type I mutation in the F11 gene is a third ancestral mutation which causes factor XI deficiency in Ashkenazi Jews

Effects of factor VIII inhibitor bypassing activity (FEIBA), recombinant factor VIIa or both on thrombin generation in normal and haemophilia A plasma

Three residues at the interface of factor XI (FXI) monomers augment covalent dimerization of FXI

Prerequisites for recombinant factor VIIa‐induced thrombin generation in plasmas deficient in factors VIII, IX or XI

Inherited factor XI deficiency confers no protection against acute myocardial infarction

Characterization of mutations causing factor VII deficiency in 61 unrelated Israeli patients

Familial factor VII deficiency with foetal and neonatal fatal cerebral haemorrhage associated with homozygosis to Gly180Arg mutation

A common ancestral mutation (C128X) occurring in 11 non‐Jewish families from the UK with factor XI deficiency

The role of factor XI in thrombin generation induced by low concentrations of tissue factor

Patients with severe factor XI deficiency have a reduced incidence of deep-vein thrombosis

Seven novel mutations in the factor XIII A‐subunit gene causing hereditary factor XIII deficiency in 10 unrelated families

Cerebrovascular events in patients with significant stenosis of the carotid artery are associated with hyperhomocysteinemia and platelet antigen-1 (Leu33Pro) polymorphism

Do platelets synthesize factor XI?

Severe factor XI deficiency caused by a Gly555 to Glu mutation (factor XI–Glu555): a cross‐reactive material positive variant defective in factor IX activation

The prevalence of factor V G1691A but not of prothrombin G20210A and methylenetetrahydrofolate reductase C677T is remarkably low in French Basques

A highly sensitive thrombin generation assay for assessment of recombinant activated factor VII therapy in haemophilia patients with an inhibitor

The Frequent 5,10-Methylenetetrahydrofolate Reductase C677T Polymorphism Is Associated with a Common Haplotype in Whites, Japanese, and Africans

Thrombophilia as a multigenic disorder

The relative frequency of hereditary thrombotic disorders among 107 patients with thrombophilia in Israel

Identification and Functional Analysis of Two Novel Mutations in the Multidrug Resistance Protein 2 Gene in Israeli Patients with Dubin-Johnson Syndrome

Clinical significance of antibodies to bovine and human thrombin and factor V after surgical use of bovine thrombin

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