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Human liver sinusoidal endothelial cells but not hepatocytes contain factor VIII

Journal of thrombosis and haemostasis, 2014-01, Vol.12 (1), p.36-42

2014

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Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

Journal of thrombosis and haemostasis, 2012-04, Vol.10 (4), p.615-621

2012

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The definition, diagnosis and management of mild hemophilia A: communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2018-12, Vol.16 (12), p.2530-2533

2018

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New challenges and best practices for the laboratory monitoring of factor VIII and factor IX replacement

International journal of laboratory hematology, 2018-05, Vol.40 (S1), p.21-29

2018

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Review article: blood platelet number and function in chronic liver disease and cirrhosis

Alimentary pharmacology & therapeutics, 2008-06, Vol.27 (11), p.1017-1029

2008

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Intensity of factor VIII treatment and the development of inhibitors in non‐severe hemophilia A patients: results of the INSIGHT case–control study

Journal of thrombosis and haemostasis, 2017-07, Vol.15 (7), p.1422-1429

2017

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Medical co-morbidities of patients with haemophilia: pain, obesity and hepatitis C

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-07, Vol.22 (S5), p.47-53

2016

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Postural control during a transition task in haemophilic children, adolescents and young adults with haemophilic ankle arthropathy

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.667-674

2018

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Mild haemophilia: a disease with many faces and many unexpected pitfalls

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-07, Vol.16 (s5), p.100-106

2010

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Comparing normal saline versus diluted heparin to lock non-valved totally implantable venous access devices in cancer patients: a randomised, non-inferiority, open trial

Annals of oncology, 2013-07, Vol.24 (7), p.1892-1899

2013

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Falling and fall risk factors in adults with haemophilia: an exploratory study

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-11, Vol.20 (6), p.836-845

2014

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Assessment of passive musculoarticular ankle stiffness in children, adolescents and young adults with haemophilic ankle arthropathy

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (3), p.e103-e112

2018

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The addition of idarucizumab to plasma samples containing dabigatran allows the use of routine coagulation assays for the diagnosis of hemostasis disorders

Journal of thrombosis and haemostasis, 2015-11, Vol.13 (11), p.2087-2092

2015

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Reliability and clinical features associated with the IPSG MRI tibiotalar and subtalar joint scores in children, adolescents and young adults with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.141-148

2018

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The adsorption of dabigatran is as efficient as addition of idarucizumab to neutralize the drug in routine coagulation assays

International journal of laboratory hematology, 2018-08, Vol.40 (4), p.442-447

2018

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Measurement of B‐domain‐deleted ReFacto AF activity with a product‐specific standard is affected by choice of reagent and patient‐specific factors

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.675-682

2018

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Biomechanical markers and theoretical concepts related to haemophilic ankle and subtalar joint arthropathy: introducing the term ‘haemophilic tarsal pan‐arthropathy’

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-07, Vol.23 (4), p.e250-e258

2017

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Practical and cost-effective measurement of B-domain deleted and full-length recombinant FVIII in the routine haemostasis laboratory

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-05, Vol.19 (3), p.e133-e138

2013

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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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Epidemiology of inhibitor formation with recombinant factor VIII replacement therapy

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-11, Vol.12 (6), p.579-590

2006

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Factor VIII deficiency does not protect against atherosclerosis

Journal of thrombosis and haemostasis, 2012-01, Vol.10 (1), p.30-37

2012

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The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG‐Arg301 to be distinguished from hypofibrinogenemia

International journal of laboratory hematology, 2017-06, Vol.39 (3), p.301-307

2017

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Acute myocardial infarction following administration of recombinant activated factor VII (Novo Seven) in a patient with haemophilia A and inhibitor

Thrombosis and haemostasis, 1999-12, Vol.82 (6), p.1775-1776

1999

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Deficits of ankle muscle strength not found in children, adolescents and young adults with haemophilic ankle arthropathy

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-09, Vol.23 (5), p.e409-e418

2017

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Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.255-263

2017

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Human liver sinusoidal endothelial cells but not hepatocytes contain factor VIII

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

The definition, diagnosis and management of mild hemophilia A: communication from the SSC of the ISTH

New challenges and best practices for the laboratory monitoring of factor VIII and factor IX replacement

Review article: blood platelet number and function in chronic liver disease and cirrhosis

Intensity of factor VIII treatment and the development of inhibitors in non‐severe hemophilia A patients: results of the INSIGHT case–control study

Medical co-morbidities of patients with haemophilia: pain, obesity and hepatitis C

Postural control during a transition task in haemophilic children, adolescents and young adults with haemophilic ankle arthropathy

Mild haemophilia: a disease with many faces and many unexpected pitfalls

Comparing normal saline versus diluted heparin to lock non-valved totally implantable venous access devices in cancer patients: a randomised, non-inferiority, open trial

Falling and fall risk factors in adults with haemophilia: an exploratory study

Assessment of passive musculoarticular ankle stiffness in children, adolescents and young adults with haemophilic ankle arthropathy

The addition of idarucizumab to plasma samples containing dabigatran allows the use of routine coagulation assays for the diagnosis of hemostasis disorders

Reliability and clinical features associated with the IPSG MRI tibiotalar and subtalar joint scores in children, adolescents and young adults with haemophilia

The adsorption of dabigatran is as efficient as addition of idarucizumab to neutralize the drug in routine coagulation assays

Measurement of B‐domain‐deleted ReFacto AF activity with a product‐specific standard is affected by choice of reagent and patient‐specific factors

Biomechanical markers and theoretical concepts related to haemophilic ankle and subtalar joint arthropathy: introducing the term ‘haemophilic tarsal pan‐arthropathy’

Practical and cost-effective measurement of B-domain deleted and full-length recombinant FVIII in the routine haemostasis laboratory

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

Epidemiology of inhibitor formation with recombinant factor VIII replacement therapy

Factor VIII deficiency does not protect against atherosclerosis

The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG‐Arg301 to be distinguished from hypofibrinogenemia

Acute myocardial infarction following administration of recombinant activated factor VII (Novo Seven) in a patient with haemophilia A and inhibitor

Deficits of ankle muscle strength not found in children, adolescents and young adults with haemophilic ankle arthropathy

Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series

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