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An open conformation of ADAMTS‐13 is a hallmark of acute acquired thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2018-02, Vol.16 (2), p.378-388

2018

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Antibodies against recombinant alpha-galactosidase A in Fabry disease: Subclass analysis and impact on response to treatment

Molecular genetics and metabolism, 2019-02, Vol.126 (2), p.162-168

2019

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Prevalence and Incidence of Non-neutralizing Antibodies in Congenital Hemophilia A- A Systematic Review and Meta-Analysis

Frontiers in immunology, 2020-05, Vol.11, p.563-563

2020

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von Willebrand factor remodeling during exocytosis from vascular endothelial cells

Journal of thrombosis and haemostasis, 2013-11, Vol.11 (11), p.2009-2019

2013

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Identification of N‐linked glycosylation and putative O‐fucosylation, C‐mannosylation sites in plasma derived ADAMTS13

Journal of thrombosis and haemostasis, 2014-05, Vol.12 (5), p.670-679

2014

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Angiogenic characteristics of blood outgrowth endothelial cells from patients with von Willebrand disease

Journal of thrombosis and haemostasis, 2015-10, Vol.13 (10), p.1854-1866

2015

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Residues Arg568 and Phe592 contribute to an antigenic surface for anti-ADAMTS13 antibodies in the spacer domain

Haematologica (Roma), 2011-11, Vol.96 (11), p.1670-1677

2011

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Early cellular interactions and immune transcriptome profiles in human factor VIII‐exposed hemophilia A mice

Journal of thrombosis and haemostasis, 2018-03, Vol.16 (3), p.533-545

2018

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VH1‐69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2009-03, Vol.7 (3), p.421-428

2009

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Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations

Journal of thrombosis and haemostasis, 2017-02, Vol.15 (2), p.246-254

2017

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Dangerous liaisons: how the immune system deals with factor VIII

Journal of thrombosis and haemostasis, 2013-01, Vol.11 (1), p.47-55

2013

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Evaluation of the role of the GPIb-IX-V receptor complex in development of the platelet storage lesion

Vox sanguinis, 2016-10, Vol.111 (3), p.247-256

2016

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Enhanced uptake of blood coagulation factor VIII containing immune complexes by antigen presenting cells

Journal of thrombosis and haemostasis, 2017-02, Vol.15 (2), p.329-340

2017

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Formation of platelet‐binding von Willebrand factor strings on non‐endothelial cells

Journal of thrombosis and haemostasis, 2012-10, Vol.10 (10), p.2168-2178

2012

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Humoral immune response to ADAMTS13 in acquired thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2011-07, Vol.9 (7), p.1285-1291

2011

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Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditions

Journal of thrombosis and haemostasis, 2008-07, Vol.6 (7), p.1135-1143

2008

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T‐cell responses in two unrelated hemophilia A inhibitor subjects include an epitope at the factor VIII R593C missense site

Journal of thrombosis and haemostasis, 2011-04, Vol.9 (4), p.689-699

2011

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Multiple B‐cell clones producing antibodies directed to the spacer and disintegrin/thrombospondin type‐1 repeat 1 (TSP1) of ADAMTS13 in a patient with acquired thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2006-11, Vol.4 (11), p.2355-2364

2006

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Phosphatidylinositol‐3,4,5‐triphosphate‐dependent Rac exchange factor 1 regulates epinephrine‐induced exocytosis of Weibel–Palade bodies

Journal of thrombosis and haemostasis, 2014-02, Vol.12 (2), p.273-281

2014

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Proteolytic cleavage of factor VIII heavy chain is required to expose the binding‐site for low‐density lipoprotein receptor‐related protein within the A2 domain

Journal of thrombosis and haemostasis, 2006-07, Vol.4 (7), p.1487-1493

2006

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Patient‐derived monoclonal antibodies directed towards beta2 glycoprotein‐1 display lupus anticoagulant activity

Journal of thrombosis and haemostasis, 2011-04, Vol.9 (4), p.738-747

2011

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Acquired thrombotic thrombocytopenic purpura. Development of an autoimmune response

Hämostaseologie, 2013-05, Vol.33 (2), p.121-130

2013

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Requirements for cellular co‐trafficking of factor VIII and von Willebrand factor to Weibel–Palade bodies

Journal of thrombosis and haemostasis, 2007-11, Vol.5 (11), p.2235-2243

2007

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Association of idiopathic venous thromboembolism with single point-mutation at Arg(506) of factor V

The Lancet (British edition), 1994-06, Vol.343 (8912), p.1535

1994

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Domain specificity of factor VIII inhibitors during immune tolerance induction in patients with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-11, Vol.16 (6), p.892-901

2010

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An open conformation of ADAMTS‐13 is a hallmark of acute acquired thrombotic thrombocytopenic purpura

Antibodies against recombinant alpha-galactosidase A in Fabry disease: Subclass analysis and impact on response to treatment

Prevalence and Incidence of Non-neutralizing Antibodies in Congenital Hemophilia A- A Systematic Review and Meta-Analysis

von Willebrand factor remodeling during exocytosis from vascular endothelial cells

Identification of N‐linked glycosylation and putative O‐fucosylation, C‐mannosylation sites in plasma derived ADAMTS13

Angiogenic characteristics of blood outgrowth endothelial cells from patients with von Willebrand disease

Residues Arg568 and Phe592 contribute to an antigenic surface for anti-ADAMTS13 antibodies in the spacer domain

Early cellular interactions and immune transcriptome profiles in human factor VIII‐exposed hemophilia A mice

VH1‐69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura

Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations

Dangerous liaisons: how the immune system deals with factor VIII

Evaluation of the role of the GPIb-IX-V receptor complex in development of the platelet storage lesion

Enhanced uptake of blood coagulation factor VIII containing immune complexes by antigen presenting cells

Formation of platelet‐binding von Willebrand factor strings on non‐endothelial cells

Humoral immune response to ADAMTS13 in acquired thrombotic thrombocytopenic purpura

Covalent regulation of ULVWF string formation and elongation on endothelial cells under flow conditions

T‐cell responses in two unrelated hemophilia A inhibitor subjects include an epitope at the factor VIII R593C missense site

Multiple B‐cell clones producing antibodies directed to the spacer and disintegrin/thrombospondin type‐1 repeat 1 (TSP1) of ADAMTS13 in a patient with acquired thrombotic thrombocytopenic purpura

Phosphatidylinositol‐3,4,5‐triphosphate‐dependent Rac exchange factor 1 regulates epinephrine‐induced exocytosis of Weibel–Palade bodies

Proteolytic cleavage of factor VIII heavy chain is required to expose the binding‐site for low‐density lipoprotein receptor‐related protein within the A2 domain

Patient‐derived monoclonal antibodies directed towards beta2 glycoprotein‐1 display lupus anticoagulant activity

Acquired thrombotic thrombocytopenic purpura. Development of an autoimmune response

Requirements for cellular co‐trafficking of factor VIII and von Willebrand factor to Weibel–Palade bodies

Association of idiopathic venous thromboembolism with single point-mutation at Arg(506) of factor V

Domain specificity of factor VIII inhibitors during immune tolerance induction in patients with haemophilia A

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