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Factor XI deficiency in humans

Journal of thrombosis and haemostasis, 2009-07, Vol.7, p.84-87

SELIGSOHN, U.

2009

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Treatment of inherited platelet disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-07, Vol.18 (s4), p.161-165

SELIGSOHN, U.

2012

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Inherited platelet disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-07, Vol.18 (s4), p.154-160

2012

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Genetic Susceptibility to Venous Thrombosis

The New England journal of medicine, 2001-04, Vol.344 (16), p.1222-1231

2001

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Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency

Journal of thrombosis and haemostasis, 2014-07, Vol.12 (7), p.1121-1130

2014

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Platelet factor XI: intracellular localization and mRNA splicing following platelet activation

Blood cells, molecules, & diseases, 2018-03, Vol.69, p.30-37

2018

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An allosteric disulfide bond is involved in enhanced activation of factor XI by protein disulfide isomerase

Journal of thrombosis and haemostasis, 2016-11, Vol.14 (11), p.2202-2211

2016

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False‐positive tests for heparin‐induced thrombocytopenia in patients with antiphospholipid syndrome and systemic lupus erythematosus

Journal of thrombosis and haemostasis, 2009-07, Vol.7 (7), p.1070-1074

2009

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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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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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An αIIb mutation in patients with Glanzmann thrombasthenia located in the N‐terminus of blade 1 of the β‐propeller (Asn2Asp) disrupts a calcium binding site in blade 6

Journal of thrombosis and haemostasis, 2011-01, Vol.9 (1), p.192-200

2011

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A mutation in the beta 3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of alpha IIb beta 3 to an active state

Journal of thrombosis and haemostasis, 2012-02, Vol.10 (2), p.289-297

2012

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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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Thrombophilic factors are not the leading cause of thrombosis in Behçet’s disease

Annals of the rheumatic diseases, 2004-11, Vol.63 (11), p.1445-1449

2004

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New observations on factor XI deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-10, Vol.10 (s4), p.184-187

2004

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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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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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A mutation in the β3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of αIIbβ3 to an active state

Journal of thrombosis and haemostasis, 2012-02, Vol.10 (2), p.289-297

2012

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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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Deciphering the mystery of combined factor V and factor VIII deficiency

Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.927-931

2006

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Factor XI deficiency

Thrombosis and haemostasis, 1993-07, Vol.70 (1), p.68

Seligsohn, U

1993

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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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Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis

The New England journal of medicine, 1996-03, Vol.334 (12), p.763-768

1996

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Rare bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (s3), p.137-142

2006

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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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Factor XI deficiency in humans

Treatment of inherited platelet disorders

Inherited platelet disorders

Genetic Susceptibility to Venous Thrombosis

Abnormal plasma clot structure and stability distinguish bleeding risk in patients with severe factor XI deficiency

Platelet factor XI: intracellular localization and mRNA splicing following platelet activation

An allosteric disulfide bond is involved in enhanced activation of factor XI by protein disulfide isomerase

False‐positive tests for heparin‐induced thrombocytopenia in patients with antiphospholipid syndrome and systemic lupus erythematosus

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

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

An αIIb mutation in patients with Glanzmann thrombasthenia located in the N‐terminus of blade 1 of the β‐propeller (Asn2Asp) disrupts a calcium binding site in blade 6

A mutation in the beta 3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of alpha IIb beta 3 to an active state

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

Thrombophilic factors are not the leading cause of thrombosis in Behçet’s disease

New observations on factor XI deficiency

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

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

A mutation in the β3 cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of αIIbβ3 to an active state

Inherited factor XI deficiency confers no protection against acute myocardial infarction

Deciphering the mystery of combined factor V and factor VIII deficiency

Factor XI deficiency

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

Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis

Rare bleeding disorders

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

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