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Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies

Journal of thrombosis and haemostasis, 2017-02, Vol.15 (2), p.312-322

2017

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Recombinant factor VIIa for patients with inhibitors to factor VIII or IX or factor VII deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 1999-07, Vol.5 (4), p.253-259

Scharrer, I

1999

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The influence of preoperative anticoagulation on outcome and quality of life after surgical treatment of chronic subdural hematoma

Journal of clinical neuroscience, 2010-08, Vol.17 (8), p.975-979

2010

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Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)

Journal of thrombosis and haemostasis, 2005-03, Vol.3 (3), p.459-464

2005

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Correlation between endogenous VWF:Ag and PK parameters and bleeding frequency in severe haemophilia A subjects during three-times-weekly prophylaxis with rFVIII-FS

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-01, Vol.20 (1), p.e15-e22

2014

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Known players, new interplay in atherogenesis: Chronic shear stress and carbamylated-LDL induce and modulate expression of atherogenic LR11 in human coronary artery endothelium

Thrombosis and haemostasis, 2014-02, Vol.111 (2), p.323-332

2014

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Long term outcome and sequelae in patients after acute thrombotic thrombocytopenic purpura episodes

Hämostaseologie, 2013-05, Vol.33 (2), p.113-120

2013

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Treatment of severe von Willebrand disease with a high‐purity von Willebrand factor concentrate (Wilfactin®): a prospective study of 50 patients

Journal of thrombosis and haemostasis, 2007-06, Vol.5 (6), p.1115-1124

2007

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Cross-cultural development and psychometric evaluation of a patient-reported health-related quality of life questionnaire for adults with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-09, Vol.14 (5), p.1023-1034

2008

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Autoimmune disorders in patients with idiopathic thrombotic thrombocytopenic purpura

Hämostaseologie, 2012-01, Vol.32 Suppl 1 (S 01), p.S86-S89

2012

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Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura

Hämostaseologie, 2014, Vol.34 (3), p.244-248

2014

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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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Hereditary thrombophilia and fetal loss: a prospective follow‐up study

Journal of thrombosis and haemostasis, 2004-04, Vol.2 (4), p.592-596

2004

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Increased fetal loss in women with heritable thrombophilia

The Lancet (British edition), 1996-10, Vol.348 (9032), p.913-916

1996

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Pharmacokinetic studies on Wilfactin®, a von Willebrand factor concentrate with a low factor VIII content treated with three virus‐inactivation/removal methods

Journal of thrombosis and haemostasis, 2005-10, Vol.3 (10), p.2219-2227

2005

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HLA genotype in patients with acquired haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-05, Vol.16 (102), p.107-112

2010

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Evaluation and clinical application of a new method for measuring activity of von Willebrand factor-cleaving metalloprotease (ADAMTS13)

Annals of hematology, 2002-08, Vol.81 (8), p.430-435

2002

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Incidence of inhibitors in haemophilia A patients - a review of recent studies of recombinant and plasma-derived factor VIII concentrates

Haemophilia : the official journal of the World Federation of Hemophilia, 1999-05, Vol.5 (3), p.145-154

1999

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Familial thrombophilia and lifetime risk of venous thrombosis

Journal of thrombosis and haemostasis, 2004-09, Vol.2 (9), p.1526-1532

2004

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Sucrose Formulated Recombinant Human Antihemophilic Factor VIII Is Safe and Efficacious for Treatment of Hemophilia A in Home Therapy: Results of a Multicenter, International, Clinical Investigation

Thrombosis and haemostasis, 2000-06, Vol.83 (6), p.811-816

2000

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Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-07, Vol.16 (4), p.675-682

2010

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Bleeding and coagulation disorders in tonsillectomies

HNO, 2012-06, Vol.60 (6), p.511-517

2012

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Experience with KOGENATE® Bayer in surgical procedures

Haemophilia : the official journal of the World Federation of Hemophilia, 2002-03, Vol.8 (s2), p.15-18

Scharrer, I.

2002

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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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Total hip replacement in patients with severe bleeding disorders. A 30 years single center experience

International orthopaedics, 2007-02, Vol.31 (1), p.17-21

2007

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Consensus on the standardization of terminology in thrombotic thrombocytopenic purpura and related thrombotic microangiopathies

Recombinant factor VIIa for patients with inhibitors to factor VIII or IX or factor VII deficiency

The influence of preoperative anticoagulation on outcome and quality of life after surgical treatment of chronic subdural hematoma

Risk of a first venous thrombotic event in carriers of a familial thrombophilic defect. The European Prospective Cohort on Thrombophilia (EPCOT)

Correlation between endogenous VWF:Ag and PK parameters and bleeding frequency in severe haemophilia A subjects during three-times-weekly prophylaxis with rFVIII-FS

Known players, new interplay in atherogenesis: Chronic shear stress and carbamylated-LDL induce and modulate expression of atherogenic LR11 in human coronary artery endothelium

Long term outcome and sequelae in patients after acute thrombotic thrombocytopenic purpura episodes

Treatment of severe von Willebrand disease with a high‐purity von Willebrand factor concentrate (Wilfactin®): a prospective study of 50 patients

Cross-cultural development and psychometric evaluation of a patient-reported health-related quality of life questionnaire for adults with haemophilia

Autoimmune disorders in patients with idiopathic thrombotic thrombocytopenic purpura

Late onset and pregnancy-induced congenital thrombotic thrombocytopenic purpura

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

Hereditary thrombophilia and fetal loss: a prospective follow‐up study

Increased fetal loss in women with heritable thrombophilia

Pharmacokinetic studies on Wilfactin®, a von Willebrand factor concentrate with a low factor VIII content treated with three virus‐inactivation/removal methods

HLA genotype in patients with acquired haemophilia A

Evaluation and clinical application of a new method for measuring activity of von Willebrand factor-cleaving metalloprotease (ADAMTS13)

Incidence of inhibitors in haemophilia A patients - a review of recent studies of recombinant and plasma-derived factor VIII concentrates

Familial thrombophilia and lifetime risk of venous thrombosis

Sucrose Formulated Recombinant Human Antihemophilic Factor VIII Is Safe and Efficacious for Treatment of Hemophilia A in Home Therapy: Results of a Multicenter, International, Clinical Investigation

Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiency

Bleeding and coagulation disorders in tonsillectomies

Experience with KOGENATE® Bayer in surgical procedures

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

Total hip replacement in patients with severe bleeding disorders. A 30 years single center experience

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