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Comparative pharmacokinetics of rVIII-SingleChain and octocog alfa (Advate®) in patients with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.730-738

2016

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Novel, human cell line-derived recombinant factor VIII (human-cl rhFVIII; Nuwiq®) in adults with severe haemophilia A: efficacy and safety

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-03, Vol.22 (2), p.225-231

2016

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Diagnostische Möglichkeiten und Grenzen der Thrombelastometrie/-graphie

Hämostaseologie, 2006, Vol.26 (S 01), p.S20-S29

2006

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Efficacy and safety of Nuwiq® (human‐cl rhFVIII) in patients with severe haemophilia A undergoing surgical procedures

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-01, Vol.24 (1), p.70-76

2018

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Fifth Åland Island conference on von Willebrand disease

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (S4), p.5-19

2018

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Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-09, Vol.16 (5), p.747-766

2010

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von Willebrand's disease: a report from a meeting in the Åland islands

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-09, Vol.18 (s6), p.1-13

2012

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Experiences with recombinant FVIIa in the emergency treatment of patients with autoimmune thrombocytopenia: a review of the literature

Annals of hematology, 2009-01, Vol.88 (1), p.11-15

2009

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Recombinant activated factor VII in treatment of bleeding complications following hematopoietic stem cell transplantation

Journal of thrombosis and haemostasis, 2005-09, Vol.3 (9), p.1935-1944

2005

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Canine haemophilia A caused by a mutation leading to a stop codon

Veterinary record, 2011-11, Vol.169 (19), p.496-496

2011

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Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgery

British journal of anaesthesia : BJA, 2011-04, Vol.106 (4), p.494-500

2011

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Managing acute bleeds in the patient with haemophilia and inhibitors: options, efficacy and safety

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-11, Vol.11 (s1), p.18-23

VON DEPKA, M.

2005

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Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

Journal of thrombosis and haemostasis, 2004-07, Vol.2 (7), p.1096-1103

2004

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Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (4), p.363-371

2006

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Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism

Blood, 2000-11, Vol.96 (10), p.3364-3368

2000

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Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate®) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery

Thrombosis and haemostasis, 2011-06, Vol.105 (6), p.1072-1079

2011

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Inhibitor Development in Patients with Hemophilia A after Continuous Infusion of FVIII Concentrates

Annals of the New York Academy of Sciences, 2005-06, Vol.1051 (1), p.498-505

2005

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Recombinant factor VIII expression in hematopoietic cells following lentiviral transduction

Gene therapy, 2003-10, Vol.10 (22), p.1917-1925

2003

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Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2007-01, Vol.13 (1), p.38-45

2007

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Possibilities and limitations of thromboelastometry/thromboelastography

Hämostaseologie, 2006, Vol.26 (S 02), p.S21-S29

2006

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Clinical relevance of genetic risk factors for thrombosis in paediatric oncology patients with central venous catheters

European journal of pediatrics, 1999-12, Vol.158 Suppl 3 (S3), p.S143-S146

1999

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Treatment patterns and cost-of-illness of severe haemophilia in patients with inhibitors in Germany

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-09, Vol.10 (5), p.499-508

2004

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European curriculum for thrombosis and haemostasis

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-01, Vol.15 (1), p.337-344

2009

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Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia

Thrombosis and haemostasis, 2001-12, Vol.86 (6), p.1360-1362

2001

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Hepatitis C plasma viral load is associated with HCV genotype but not with HIV coinfection

Journal of medical virology, 1996-04, Vol.48 (4), p.339-343

1996

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Comparative pharmacokinetics of rVIII-SingleChain and octocog alfa (Advate®) in patients with severe haemophilia A

Novel, human cell line-derived recombinant factor VIII (human-cl rhFVIII; Nuwiq®) in adults with severe haemophilia A: efficacy and safety

Diagnostische Möglichkeiten und Grenzen der Thrombelastometrie/-graphie

Efficacy and safety of Nuwiq® (human‐cl rhFVIII) in patients with severe haemophilia A undergoing surgical procedures

Fifth Åland Island conference on von Willebrand disease

Non-genetic risk factors and the development of inhibitors in haemophilia: a comprehensive review and consensus report

von Willebrand's disease: a report from a meeting in the Åland islands

Experiences with recombinant FVIIa in the emergency treatment of patients with autoimmune thrombocytopenia: a review of the literature

Recombinant activated factor VII in treatment of bleeding complications following hematopoietic stem cell transplantation

Canine haemophilia A caused by a mutation leading to a stop codon

Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgery

Managing acute bleeds in the patient with haemophilia and inhibitors: options, efficacy and safety

Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

Current European practice in immune tolerance induction therapy in patients with haemophilia and inhibitors

Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism

Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate®) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery

Inhibitor Development in Patients with Hemophilia A after Continuous Infusion of FVIII Concentrates

Recombinant factor VIII expression in hematopoietic cells following lentiviral transduction

Current use of by-passing agents in Europe in the management of acute bleeds in patients with haemophilia and inhibitors

Possibilities and limitations of thromboelastometry/thromboelastography

Clinical relevance of genetic risk factors for thrombosis in paediatric oncology patients with central venous catheters

Treatment patterns and cost-of-illness of severe haemophilia in patients with inhibitors in Germany

European curriculum for thrombosis and haemostasis

Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia

Hepatitis C plasma viral load is associated with HCV genotype but not with HIV coinfection

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