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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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Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa

Journal of thrombosis and haemostasis, 2004-01, Vol.2 (1), p.102-110

2004

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A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.766-773

2006

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Fibrinogen concentrate substitution therapy in patients with massive haemorrhage and low plasma fibrinogen concentrations

British journal of anaesthesia : BJA, 2008-12, Vol.101 (6), p.769-773

2008

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Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

Haematologica (Roma), 2013-04, Vol.98 (4), p.538-544

2013

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Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.752-759

2016

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Congenital factor VII deficiency: therapy with recombinant activated factor VII - a critical appraisal

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-01, Vol.12 (1), p.19-27

2006

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Progression of haemophilic arthropathy in children: a Lithuanian - Danish comparative study

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-03, Vol.19 (2), p.212-218

2013

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Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-11, Vol.21 (6), p.e513-e517

2015

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Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven®] in elective orthopaedic surgery in haemophilic patients with inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-03, Vol.15 (2), p.501-508

2009

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Utility of the Haemophilia Joint Health Score in study of episodically treated boys with severe haemophilia A and B in Lithuania

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-05, Vol.16 (3), p.479-486

2010

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Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.774-782

2006

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Invasive procedures and minor surgery in factor VII deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.e63-e65

2012

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Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1VWD)

Journal of thrombosis and haemostasis, 2007-04, Vol.5 (4), p.715-721

2007

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Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

Thrombosis research, 2010-09, Vol.126 (3), p.227-231

2010

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Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment

Haemophilia : the official journal of the World Federation of Hemophilia, 2007-05, Vol.13 (3), p.334-336

2007

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Break‐through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia A

Journal of thrombosis and haemostasis, 2009-03, Vol.7 (3), p.413-420

2009

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Comparative pharmacokinetics of plasma‐ and albumin‐free recombinant factor VIII in children and adults: the influence of blood sampling schedule on observed age‐related differences and implications for dose tailoring

Journal of thrombosis and haemostasis, 2010-04, Vol.8 (4), p.730-736

2010

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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Thrombosis and haemostasis, 2005-03, Vol.93 (3), p.481-487

2005

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Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients

Blood coagulation & fibrinolysis, 1999-07, Vol.10 (5), p.251

1999

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Treatment of Acute Bleeding Episodes with rFVIIa

Vox sanguinis, 1999-01, Vol.77 (Suppl 1), p.42-46

1999

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The 20210 A allele of the prothrombin gene is not a risk factor for juvenile stroke in the Danish population

Blood coagulation & fibrinolysis, 1998-10, Vol.9 (7), p.663-664

1998

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Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Blood, 2000-03, Vol.95 (6), p.2000-2007

2000

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Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation

Journal of internal medicine, 1994-05, Vol.235 (5), p.443-450

1994

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Antibodies to heterologous proteins in hemophilia A patients receiving recombinant factor VIII (Recombinate)

Thrombosis and haemostasis, 2002-04, Vol.87 (4), p.626-634

2002

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

Whole blood clot formation phenotypes in hemophilia A and rare coagulation disorders. Patterns of response to recombinant factor VIIa

A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Fibrinogen concentrate substitution therapy in patients with massive haemorrhage and low plasma fibrinogen concentrations

Prophylaxis in congenital factor VII deficiency: indications, efficacy and safety. Results from the Seven Treatment Evaluation Registry (STER)

Women with congenital factor VII deficiency: clinical phenotype and treatment options from two international studies

Congenital factor VII deficiency: therapy with recombinant activated factor VII - a critical appraisal

Progression of haemophilic arthropathy in children: a Lithuanian - Danish comparative study

Replacement therapy in inherited factor VII deficiency: occurrence of adverse events and relation with surgery

Consensus protocol for the use of recombinant activated factor VII [eptacog alfa (activated); NovoSeven®] in elective orthopaedic surgery in haemophilic patients with inhibitors

Utility of the Haemophilia Joint Health Score in study of episodically treated boys with severe haemophilia A and B in Lithuania

Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD

Invasive procedures and minor surgery in factor VII deficiency

Impact of plasma von Willebrand factor levels in the diagnosis of type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1VWD)

Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

Severe factor X deficiency in a pair of siblings: clinical presentation, phenotypic and genotypic features, prenatal diagnosis and treatment

Break‐through bleeding in relation to predicted factor VIII levels in patients receiving prophylactic treatment for severe hemophilia A

Comparative pharmacokinetics of plasma‐ and albumin‐free recombinant factor VIII in children and adults: the influence of blood sampling schedule on observed age‐related differences and implications for dose tailoring

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients

Treatment of Acute Bleeding Episodes with rFVIIa

The 20210 A allele of the prothrombin gene is not a risk factor for juvenile stroke in the Danish population

Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor

Mild haemophilia A in Iceland: clinical genetic studies of three families with the same mutation

Antibodies to heterologous proteins in hemophilia A patients receiving recombinant factor VIII (Recombinate)

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