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Riboflavin and amotosalen photochemical treatments of platelet concentrates reduce thrombus formation kinetics in vitro

Vox sanguinis, 2015-05, Vol.108 (4), p.328-339

2015

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Linker regions and flexibility around the metalloprotease domain account for conformational activation of ADAMTS‐13

Journal of thrombosis and haemostasis, 2015-11, Vol.13 (11), p.2063-2075

2015

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ADAMTS‐13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences

Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.955-962

2006

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ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission

Haematologica (Roma), 2008-02, Vol.93 (2), p.232-239

2008

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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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High platelet content can increase storage lesion rates following Intercept pathogen inactivation primarily in platelet concentrates prepared by apheresis

Vox sanguinis, 2017-11, Vol.112 (8), p.751-758

2017

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Comparison of three commercially available buffy coat pooling sets for the preparation of platelet concentrates

Vox sanguinis, 2018-08, Vol.113 (6), p.555-561

2018

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Multi‐step binding of ADAMTS‐13 to von Willebrand factor

Journal of thrombosis and haemostasis, 2009-12, Vol.7 (12), p.2088-2095

2009

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The contribution of von Willebrand factor-GPIbα interactions to persistent aggregate formation in apheresis platelet concentrates

Vox sanguinis, 2016-05, Vol.110 (4), p.344-351

2016

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The contribution of von Willebrand factor-GPIb[alpha] interactions to persistent aggregate formation in apheresis platelet concentrates

Vox sanguinis, 2016-05, Vol.110 (4), p.344

2016

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Persistent aggregates in apheresis platelet concentrates are commonly collected from donors with a history of aggregate donation

Vox sanguinis, 2016-11, Vol.111 (4), p.431-433

2016

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Oxygen removal during pathogen inactivation with riboflavin and UV light preserves protein function in plasma for transfusion

Vox sanguinis, 2014-05, Vol.106 (4), p.307-315

2014

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Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpura

Journal of thrombosis and haemostasis, 2010-09, Vol.8 (9), p.2053-2062

2010

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Persistent aggregates in apheresis platelet concentrates

Vox sanguinis, 2015-05, Vol.108 (4), p.368-377

2015

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The distal carboxyterminal domains of murine ADAMTS13 influence proteolysis of platelet‐decorated VWF strings in vivo

Journal of thrombosis and haemostasis, 2010-10, Vol.8 (10), p.2305-2312

2010

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Active platelet‐binding conformation of plasma von Willebrand factor in young women with acute myocardial infarction

Journal of thrombosis and haemostasis, 2010-07, Vol.8 (7), p.1653-1656

2010

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High platelet content can increase storage lesion rates following Intercept pathogen inactivation primarily in platelet concentrates prepared by apheresis

Vox sanguinis, 2018-10, Vol.113 (7), p.708-708

2018

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Development of monoclonal antibodies that inhibit platelet adhesion or aggregation as potential anti-thrombotic drugs

Cardiovascular & hematological disorders drug targets, 2006-09, Vol.6 (3), p.191-207

2006

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The contribution of von Willebrand factor– GPI bα interactions to persistent aggregate formation in apheresis platelet concentrates

Vox sanguinis, 2016-05, Vol.110 (4), p.344-351

2016

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ADAMTS‐13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences

Journal of thrombosis and haemostasis, 2006-05, Vol.4 (5), p.955-962

2006

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Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub)endothelial VWF from cleavage by ADAMTS13

Blood, 2006-02, Vol.107 (3), p.955-964

2006

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Alteration of ADAMTS13 antigen levels in patients with idiopathic thrombotic thrombocytopenic purpura, idiopathic thrombocytopenic purpura and systemic lupus erythematosus

Thrombosis and haemostasis, 2006-04, Vol.95 (4), p.749-750

2006

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Multi-step binding of ADAMTS13 to VWF

Journal of thrombosis and haemostasis, 2009-09, Vol.7 (12)

2009

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Time use of stroke patients in an intensive rehabilitation unit: a comparison between a Belgian and a Swiss setting

Disability and rehabilitation, 2000-03, Vol.22 (4), p.181-186

de Weerdt, B. Selz, G. Nuyens, F. Staes, D. Swinnen, A. van de Winckel, A. Nieuwboer, R. Lysens, H. Feys, W.

2000

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Riboflavin and amotosalen photochemical treatments of platelet concentrates reduce thrombus formation kinetics in vitro

Linker regions and flexibility around the metalloprotease domain account for conformational activation of ADAMTS‐13

ADAMTS‐13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences

ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission

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

High platelet content can increase storage lesion rates following Intercept pathogen inactivation primarily in platelet concentrates prepared by apheresis

Comparison of three commercially available buffy coat pooling sets for the preparation of platelet concentrates

Multi‐step binding of ADAMTS‐13 to von Willebrand factor

The contribution of von Willebrand factor-GPIbα interactions to persistent aggregate formation in apheresis platelet concentrates

The contribution of von Willebrand factor-GPIb[alpha] interactions to persistent aggregate formation in apheresis platelet concentrates

Persistent aggregates in apheresis platelet concentrates are commonly collected from donors with a history of aggregate donation

Oxygen removal during pathogen inactivation with riboflavin and UV light preserves protein function in plasma for transfusion

Inactivation of ADAMTS13 by plasmin as a potential cause of thrombotic thrombocytopenic purpura

Persistent aggregates in apheresis platelet concentrates

The distal carboxyterminal domains of murine ADAMTS13 influence proteolysis of platelet‐decorated VWF strings in vivo

Active platelet‐binding conformation of plasma von Willebrand factor in young women with acute myocardial infarction

Aggregates in platelet concentrates

High platelet content can increase storage lesion rates following Intercept pathogen inactivation primarily in platelet concentrates prepared by apheresis

Development of monoclonal antibodies that inhibit platelet adhesion or aggregation as potential anti-thrombotic drugs

The contribution of von Willebrand factor– GPI bα interactions to persistent aggregate formation in apheresis platelet concentrates

ADAMTS‐13 plasma level determination uncovers antigen absence in acquired thrombotic thrombocytopenic purpura and ethnic differences

Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub)endothelial VWF from cleavage by ADAMTS13

Alteration of ADAMTS13 antigen levels in patients with idiopathic thrombotic thrombocytopenic purpura, idiopathic thrombocytopenic purpura and systemic lupus erythematosus

Multi-step binding of ADAMTS13 to VWF

Time use of stroke patients in an intensive rehabilitation unit: a comparison between a Belgian and a Swiss setting

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