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Von Willebrand factor and angiogenesis: basic and applied issues

Journal of thrombosis and haemostasis, 2017-01, Vol.15 (1), p.13-20

2017

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Can you grow out of von Willebrand disease?

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-11, Vol.23 (6), p.807-809

Laffan, M.

2017

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Sleep-disordered breathing, hypoxia, and risk of mild cognitive impairment and dementia in older women

JAMA : the journal of the American Medical Association, 2011-08, Vol.306 (6), p.613

2011

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Guidelines on the laboratory aspects of assays used in haemostasis and thrombosis

International journal of laboratory hematology, 2013-02, Vol.35 (1), p.1-13

2013

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Safety and pharmacokinetics of anti‐TFPI antibody (concizumab) in healthy volunteers and patients with hemophilia: a randomized first human dose trial

Journal of thrombosis and haemostasis, 2015-05, Vol.13 (5), p.743-754

2015

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Measurement of the in situ ply fracture toughness associated with mode I fibre tensile failure in FRP. Part I: Data reduction

Composites science and technology, 2010-04, Vol.70 (4), p.606-613

2010

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A Systematic Review of Operative Team Familiarity on Metrics of Efficiency, Patient Outcomes, Cost, and Team Satisfaction

Annals of surgery, 2022-12, Vol.276 (6), p.e674

2022

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Modelling the R-curve effect and its specimen-dependence

International journal of solids and structures, 2011-06, Vol.48 (11), p.1767-1777

2011

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Measurement of the in situ ply fracture toughness associated with mode I fibre tensile failure in FRP. Part II: Size and lay-up effects

Composites science and technology, 2010-04, Vol.70 (4), p.614-621

2010

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Site‐specific analysis of von Willebrand factor O‐glycosylation

Journal of thrombosis and haemostasis, 2016-04, Vol.14 (4), p.733-746

2016

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Should we abandon the APTT for monitoring unfractionated heparin?

Thrombosis research, 2017-09, Vol.157, p.157-161

2017

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Light Exposure Patterns in Healthy Older and Young Adults

Journal of biological rhythms, 2010-04, Vol.25 (2), p.113-122

2010

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Translaminar fracture toughness testing of composites: A review

Polymer testing, 2012-05, Vol.31 (3), p.481-489

2012

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ADAMTS‐13 glycans and conformation‐dependent activity

Journal of thrombosis and haemostasis, 2017-06, Vol.15 (6), p.1155-1166

2017

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International Society on Thrombosis and Haemostasis core curriculum project: core competencies in clinical thrombosis and hemostasis

Journal of thrombosis and haemostasis, 2016-01, Vol.14 (1), p.3-27

2016

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The relationship between ABO histo-blood group, factor VIII and von Willebrand factor

Transfusion medicine (Oxford, England), 2001-08, Vol.11 (4), p.343-351

2001

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Survey evaluating clinical equipoise around platelet transfusion after head injury and traumatic intracranial haemorrhage (ICH) in patients on antiplatelet medications

Emergency medicine journal : EMJ, 2022-03, Vol.39 (3), p.220

2022

Volltextzugriff (PDF)

The plasma von Willebrand factor O‐glycome comprises a surprising variety of structures including ABH antigens and disialosyl motifs

Journal of thrombosis and haemostasis, 2010-01, Vol.8 (1), p.137-145

2010

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Real-world outcomes with recombinant factor VIIa treatment of acute bleeds in haemophilia patients with inhibitors: results from the international ONE registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.571-577

2013

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A low balance between microparticles expressing tissue factor pathway inhibitor and tissue factor is associated with thrombosis in Behçet's Syndrome

Scientific reports, 2016-12, Vol.6 (1), p.38104-38104, Article 38104

2016

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Thrombosis and Behçet’s syndrome in non-endemic regions

Rheumatology (Oxford, England), 2010-11, Vol.49 (11), p.2003-2004

2010

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Health Care Utilization and Cost Outcomes of a Comprehensive Dementia Care Program for Medicare Beneficiaries

JAMA internal medicine, 2019-02, Vol.179 (2), p.161

2019

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Making contact with microparticles

Journal of thrombosis and haemostasis, 2012-07, Vol.10 (7), p.1352-1354

2012

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Thrombin generation and phenotypic correlation in haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-07, Vol.11 (4), p.326-334

2005

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The von Willebrand factor predicted unpaired cysteines are essential for secretion

Journal of thrombosis and haemostasis, 2014-02, Vol.12 (2), p.246-254

2014

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Von Willebrand factor and angiogenesis: basic and applied issues

Can you grow out of von Willebrand disease?

Sleep-disordered breathing, hypoxia, and risk of mild cognitive impairment and dementia in older women

Guidelines on the laboratory aspects of assays used in haemostasis and thrombosis

Safety and pharmacokinetics of anti‐TFPI antibody (concizumab) in healthy volunteers and patients with hemophilia: a randomized first human dose trial

Measurement of the in situ ply fracture toughness associated with mode I fibre tensile failure in FRP. Part I: Data reduction

A Systematic Review of Operative Team Familiarity on Metrics of Efficiency, Patient Outcomes, Cost, and Team Satisfaction

Modelling the R-curve effect and its specimen-dependence

Measurement of the in situ ply fracture toughness associated with mode I fibre tensile failure in FRP. Part II: Size and lay-up effects

Site‐specific analysis of von Willebrand factor O‐glycosylation

Should we abandon the APTT for monitoring unfractionated heparin?

Light Exposure Patterns in Healthy Older and Young Adults

Translaminar fracture toughness testing of composites: A review

ADAMTS‐13 glycans and conformation‐dependent activity

International Society on Thrombosis and Haemostasis core curriculum project: core competencies in clinical thrombosis and hemostasis

The relationship between ABO histo-blood group, factor VIII and von Willebrand factor

Survey evaluating clinical equipoise around platelet transfusion after head injury and traumatic intracranial haemorrhage (ICH) in patients on antiplatelet medications

The plasma von Willebrand factor O‐glycome comprises a surprising variety of structures including ABH antigens and disialosyl motifs

Real-world outcomes with recombinant factor VIIa treatment of acute bleeds in haemophilia patients with inhibitors: results from the international ONE registry

A low balance between microparticles expressing tissue factor pathway inhibitor and tissue factor is associated with thrombosis in Behçet's Syndrome

Thrombosis and Behçet’s syndrome in non-endemic regions

Health Care Utilization and Cost Outcomes of a Comprehensive Dementia Care Program for Medicare Beneficiaries

Making contact with microparticles

Thrombin generation and phenotypic correlation in haemophilia A

The von Willebrand factor predicted unpaired cysteines are essential for secretion

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