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Red-blood-cell alloimmunization and number of red-blood-cell transfusions

Vox sanguinis, 2012-02, Vol.102 (2), p.144-149

2012

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Does plasma fibrinogen increase thrombotic tendency?

European journal of clinical investigation, 2002-10, Vol.32 (10), p.721-722

Bom, J. G. van der

2002

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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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Can long‐term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands

British journal of haematology, 2005-07, Vol.130 (1), p.107-112

2005

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Mitochondrial oxygen tension in critically ill patients receiving red blood cell transfusions: a multicenter observational cohort study

Intensive care medicine experimental, 2024-07, Vol.12 (1), p.61-11, Article 61

2024

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Clinically relevant differences between assays for von Willebrand factor activity

Journal of thrombosis and haemostasis, 2018-12, Vol.16 (12), p.2413-2424

2018

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Management of postpartum hemorrhage: how to improve maternal outcomes?

Journal of thrombosis and haemostasis, 2018-08, Vol.16 (8), p.1523-1534

2018

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Impact of restrictive platelet transfusion strategies on transfusion rates: A cohort study in very preterm infants

Transfusion (Philadelphia, Pa.), 2024-08, Vol.64 (8), p.1421-1427

2024

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Factor VIII products and inhibitor development in previously treated patients with severe or moderately severe hemophilia A: a systematic review

Journal of thrombosis and haemostasis, 2018-06, Vol.16 (6), p.1055-1068

2018

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Mortality after transfusions, relation to donor sex

Vox sanguinis, 2011-10, Vol.101 (3), p.221-229

2011

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Risk factors and time delay associated with cardiac device infections: Leiden device registry

Heart (British Cardiac Society), 2009-05, Vol.95 (9), p.715-720

2009

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Analysis of low frequency bleeding data: the association of joint bleeds according to baseline FVIII activity levels

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-01, Vol.17 (1), p.41-44

2011

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Membrane sweeping and prevention of post‐term pregnancy in low‐risk pregnancies: a randomised controlled trial

BJOG : an international journal of obstetrics and gynaecology, 2006-04, Vol.113 (4), p.402-408

2006

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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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Mortality caused by intracranial bleeding in non‐severe hemophilia A patients

Journal of thrombosis and haemostasis, 2017-06, Vol.15 (6), p.1115-1122

2017

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Treatment characteristics and the risk of inhibitor development: a multicenter cohort study among previously untreated patients with severe hemophilia A

Journal of thrombosis and haemostasis, 2007-07, Vol.5 (7), p.1383-1390

2007

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Long‐term outcome of individualized prophylactic treatment of children with severe haemophilia

British journal of haematology, 2001-03, Vol.112 (3), p.561-565

2001

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Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.e185-e192

2015

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Mortality and causes of death in patients with hemophilia, 1992-2001: a prospective cohort study

Journal of thrombosis and haemostasis, 2006-03, Vol.4 (3), p.510-516

2006

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Surgery and inhibitor development in hemophilia A: a systematic review

Journal of thrombosis and haemostasis, 2011-10, Vol.9 (10), p.1948-1958

2011

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Variation in red cell transfusion practice in the intensive care unit – An international survey

Journal of critical care, 2020-02, Vol.55, p.140-144

2020

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Variation in red cell transfusion decisions in the intensive care unit – a nationwide survey in the Netherlands

Vox sanguinis, 2018-05, Vol.113 (4), p.378-385

2018

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Prospective validation of the EuroSCORE II risk model in a single Dutch cardiac surgery centre

Netherlands heart journal, 2018-11, Vol.26 (11), p.540-551

2018

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Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice

Journal of thrombosis and haemostasis, 2008-12, Vol.6 (12), p.2048-2054

2008

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Defining patient value in haemophilia care

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.516-518

2018

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Red-blood-cell alloimmunization and number of red-blood-cell transfusions

Does plasma fibrinogen increase thrombotic tendency?

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

Can long‐term prophylaxis for severe haemophilia be stopped in adulthood? Results from Denmark and the Netherlands

Mitochondrial oxygen tension in critically ill patients receiving red blood cell transfusions: a multicenter observational cohort study

Clinically relevant differences between assays for von Willebrand factor activity

Management of postpartum hemorrhage: how to improve maternal outcomes?

Impact of restrictive platelet transfusion strategies on transfusion rates: A cohort study in very preterm infants

Factor VIII products and inhibitor development in previously treated patients with severe or moderately severe hemophilia A: a systematic review

Mortality after transfusions, relation to donor sex

Risk factors and time delay associated with cardiac device infections: Leiden device registry

Analysis of low frequency bleeding data: the association of joint bleeds according to baseline FVIII activity levels

Membrane sweeping and prevention of post‐term pregnancy in low‐risk pregnancies: a randomised controlled trial

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

Mortality caused by intracranial bleeding in non‐severe hemophilia A patients

Treatment characteristics and the risk of inhibitor development: a multicenter cohort study among previously untreated patients with severe hemophilia A

Long‐term outcome of individualized prophylactic treatment of children with severe haemophilia

Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study

Mortality and causes of death in patients with hemophilia, 1992-2001: a prospective cohort study

Surgery and inhibitor development in hemophilia A: a systematic review

Variation in red cell transfusion practice in the intensive care unit – An international survey

Variation in red cell transfusion decisions in the intensive care unit – a nationwide survey in the Netherlands

Prospective validation of the EuroSCORE II risk model in a single Dutch cardiac surgery centre

Risk stratification for inhibitor development at first treatment for severe hemophilia A: a tool for clinical practice

Defining patient value in haemophilia care

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