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Joint disease in haemophilia: Pathophysiology, pain and imaging

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-05, Vol.24 (S6), p.44-49

2018

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Diagnostic and prognostic value of factor VIII binding antibodies in acquired hemophilia A: data from the GTH‐AH 01/2010 study

Journal of thrombosis and haemostasis, 2016-05, Vol.14 (5), p.940-947

2016

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Pain management in patients with haemophilia: a European survey

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-09, Vol.18 (5), p.743-752

2012

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The impact of social factors on outcomes in patients with bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.46-53

2016

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Expression and release of platelet protein disulphide isomerase in patients with haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.e537-e544

2016

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Current view and outcome of ITI therapy - A change over time?

Thrombosis research, 2016-12, Vol.148, p.38-44

2016

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Management of acute haemarthrosis in haemophilia A without inhibitors: literature review, European survey and recommendations

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-05, Vol.17 (3), p.383-392

2011

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Successful second ITI with factor IX and combined immunosuppressive therapy. A patient with severe haemophilia B and recurrence of a factor IX inhibitor

Hämostaseologie, 2014, Vol.34 Suppl 1, p.S5

2014

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Relevant bleeding diathesis due to acquired factor XIII deficiency

Hämostaseologie, 2013-01, Vol.33 Suppl 1, p.S50

2013

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Thromboembolische Komplikationen – Prophylaxe und Therapie im Fokus

Der Onkologe, 2009-02, Vol.15 (2), p.150-156

2009

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Relationship between rectal temperature at first treatment for bovine respiratory disease complex in feedlot calves and the probability of not finishing the production cycle

Journal of the American Veterinary Medical Association, 2014-12, Vol.245 (11), p.1279

2014

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Successful eradication of a FVIII inhibitor in a 60-year-old patient with mild haemophilia A using single-agent prednisolone

Hämostaseologie, 2012-01, Vol.32 Suppl 1, p.S48

2012

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Corporations as Stepfamilies: A New Metaphor for Explaining the Fate of Merged and Acquired Companies

Academy of Management perspectives, 2005-08, Vol.19 (3), p.23-37

2005

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Inhibitor-Immunology-Study. Different HLA-types seem to be involved in the inhibitor development in haemophilia A

Hämostaseologie, 2008-10, Vol.28 Suppl 1, p.S26

2008

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PB0670 Nationwide Survey on the Care Reality of People with Mild Hemophilia A and B in Germany - The Burden of Mild Hemophilia

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101167, Article 101167

2023

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Inhibitor-immunology-study. Evaluation of inhibitor development in haemophilia B

Hämostaseologie, 2011-11, Vol.31 Suppl 1, p.S57

2011

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Haemostatic aspects in clinical oncology

Hämostaseologie, 2008-12, Vol.28 (5), p.472

2008

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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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PB0643 Efficacy of Emicizumab Prophylaxis in Patients with Severe Hemophilia A in Germany: Follow-up Evaluation of Real-Life-Data Documented by Smart Medication eDiary

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101183, Article 101183

2023

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Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.110-120

2016

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LB 01.2 Emicizumab Prophylaxis Instead of Immunosuppressive Therapy in Patients with Acquired Hemophilia A (AHA)

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.100289, Article 100289

2023

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Outcome measures in European patients with haemophilia: Survey of implementation in routine clinical practice, perception of relevance and recommendations by European treaters in the EHTSB

Haemophilia : the official journal of the World Federation of Hemophilia, 2017-03, Vol.23 (2), p.222-229

2017

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Purpura Fulminans Triggered by the Formation of Anti-Endothelial Autoantibodies in a Patient with Chronic Lymphocytic Leukemia

Annals of hematology & oncology, 2022-03, Vol.9 (1)

2022

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Neonatal bleeding in haemophilia: a European cohort study

British journal of haematology, 2012-02, Vol.156 (3), p.374-382

2012

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Sequential combined bypassing therapy is safe and effective in the treatment of unresponsive bleeding in adults and children with haemophilia and inhibitors

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-07, Vol.17 (4), p.630-635

2011

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Joint disease in haemophilia: Pathophysiology, pain and imaging

Diagnostic and prognostic value of factor VIII binding antibodies in acquired hemophilia A: data from the GTH‐AH 01/2010 study

Pain management in patients with haemophilia: a European survey

The impact of social factors on outcomes in patients with bleeding disorders

Expression and release of platelet protein disulphide isomerase in patients with haemophilia A

Current view and outcome of ITI therapy - A change over time?

Management of acute haemarthrosis in haemophilia A without inhibitors: literature review, European survey and recommendations

Successful second ITI with factor IX and combined immunosuppressive therapy. A patient with severe haemophilia B and recurrence of a factor IX inhibitor

Relevant bleeding diathesis due to acquired factor XIII deficiency

Thromboembolische Komplikationen – Prophylaxe und Therapie im Fokus

Relationship between rectal temperature at first treatment for bovine respiratory disease complex in feedlot calves and the probability of not finishing the production cycle

Successful eradication of a FVIII inhibitor in a 60-year-old patient with mild haemophilia A using single-agent prednisolone

Corporations as Stepfamilies: A New Metaphor for Explaining the Fate of Merged and Acquired Companies

Inhibitor-Immunology-Study. Different HLA-types seem to be involved in the inhibitor development in haemophilia A

PB0670 Nationwide Survey on the Care Reality of People with Mild Hemophilia A and B in Germany - The Burden of Mild Hemophilia

Inhibitor-immunology-study. Evaluation of inhibitor development in haemophilia B

Haemostatic aspects in clinical oncology

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

PB0643 Efficacy of Emicizumab Prophylaxis in Patients with Severe Hemophilia A in Germany: Follow-up Evaluation of Real-Life-Data Documented by Smart Medication eDiary

Practical aspects of DDAVP use in patients with von Willebrand Disease undergoing invasive procedures: a European survey

LB 01.2 Emicizumab Prophylaxis Instead of Immunosuppressive Therapy in Patients with Acquired Hemophilia A (AHA)

Outcome measures in European patients with haemophilia: Survey of implementation in routine clinical practice, perception of relevance and recommendations by European treaters in the EHTSB

Purpura Fulminans Triggered by the Formation of Anti-Endothelial Autoantibodies in a Patient with Chronic Lymphocytic Leukemia

Neonatal bleeding in haemophilia: a European cohort study

Sequential combined bypassing therapy is safe and effective in the treatment of unresponsive bleeding in adults and children with haemophilia and inhibitors

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