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Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice

Journal of thrombosis and haemostasis, 2012-07, Vol.10 (7), p.1335-1341

2012

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Identification and long-term observation of early joint damage by magnetic resonance imaging in clinically asymptomatic joints in patients with haemophilia A or B despite prophylaxis

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.369-374

2012

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New early prophylaxis regimen that avoids immunological danger signals can reduce FVIII inhibitor development

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-03, Vol.16 (2), p.256-262

2010

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Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma‐derived or recombinant factor VIII concentrates: a systematic review

Journal of thrombosis and haemostasis, 2010-06, Vol.8 (6), p.1256-1265

2010

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Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies

European journal of pediatrics, 2012-09, Vol.171 (9), p.1339-1348

2012

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Early prophylaxis/FVIII tolerization regimen that avoids immunological danger signals is still effective in minimizing FVIII inhibitor developments in previously untreated patients - long-term follow-up and continuing experience

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-01, Vol.18 (1), p.e18-e20

2012

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Vaccinations are not associated with inhibitor development in boys with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-03, Vol.24 (2), p.283-290

2018

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Validation of the Haemophilia & Exercise Project‐Test‐Questionnaire (HEP‐Test‐Q)—An instrument for the assessment of subjective physical functioning in children with haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-11, Vol.24 (6), p.888-895

2018

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Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-01, Vol.19 (1), p.76-81

2013

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How to achieve full prophylaxis in young boys with severe haemophilia A: different regimens and their effect on early bleeding and venous access

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.444-450

2015

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Using routine Haemophilia Joint Health Score for international comparisons of haemophilia outcome: standardization is needed

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-01, Vol.22 (1), p.142-147

2016

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Stroke alarm-Arterial ischemic stroke as one of the most time-critical emergencies in children and adolescents

Nervenarzt, 2022-02, Vol.93 (2), p.158

2022

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Motivational effects of top-rope climbing therapy under individualized prophylaxis: a pilot study in young adults with severe haemophilia

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-11, Vol.21 (6), p.e504-e507

2015

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Prospects for research in haemophilia with real‐world data—An analysis of German registry and secondary data

Haemophilia : the official journal of the World Federation of Hemophilia, 2018-07, Vol.24 (4), p.584-594

2018

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The EPIC study: a lesson to learn

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-09, Vol.21 (5), p.622-628

2015

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Aspirin versus low-dose low-molecular-weight heparin : Antithrombotic therapy in pediatric ischemic stroke patients : A prospective follow-up study

Stroke (1970), 2001-11, Vol.32 (11), p.2554-2558

2001

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Blood coagulation disorders in children

Hämostaseologie, 2008-12, Vol.28 (5), p.465

Kurnik, K

2008

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Climbing therapy under PK-tailored prophylaxis

Hämostaseologie, 2014-01, Vol.34 Suppl 1, p.S13

2014

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Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors

Thrombosis and haemostasis, 2001-02, Vol.85 (2), p.218

2001

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Repeated coagulation testing in children. Does it improve the diagnostic value?

Hämostaseologie, 2011-11, Vol.31 Suppl 1, p.S51

2011

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Continuous infusion of factor concentrates in children with haemophilia A in comparison with bolus injections

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-05, Vol.12 (3), p.212-217

2006

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Treatment of children with severe haemophilia A and inhibitors: a health economic evaluation for Germany

Klinische Padiatrie, 2013-05, Vol.225 (3), p.152

2013

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Immune tolerance induction with a factor VIII concentrate containing von Willebrand factor (Haemoctin SDH®) in 14 patients with severe haemophilia A

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-09, Vol.17 (5), p.e837-e840

2011

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Notfall-Neuropädiatrie – Der arteriell ischämische Schlaganfall als einer der zeitkritischsten Notfälle bei Kindern und Jugendlichen

Nervenarzt, 2022-02, Vol.93 (2), p.158-166

2022

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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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Prospective evaluation of a pediatric bleeding questionnaire and the ISTH bleeding assessment tool in children and parents in routine clinical practice

Identification and long-term observation of early joint damage by magnetic resonance imaging in clinically asymptomatic joints in patients with haemophilia A or B despite prophylaxis

New early prophylaxis regimen that avoids immunological danger signals can reduce FVIII inhibitor development

Rate of inhibitor development in previously untreated hemophilia A patients treated with plasma‐derived or recombinant factor VIII concentrates: a systematic review

Hereditary angioedema (HAE) in children and adolescents—a consensus on therapeutic strategies

Early prophylaxis/FVIII tolerization regimen that avoids immunological danger signals is still effective in minimizing FVIII inhibitor developments in previously untreated patients - long-term follow-up and continuing experience

Vaccinations are not associated with inhibitor development in boys with severe haemophilia A

Validation of the Haemophilia & Exercise Project‐Test‐Questionnaire (HEP‐Test‐Q)—An instrument for the assessment of subjective physical functioning in children with haemophilia

Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)

How to achieve full prophylaxis in young boys with severe haemophilia A: different regimens and their effect on early bleeding and venous access

Using routine Haemophilia Joint Health Score for international comparisons of haemophilia outcome: standardization is needed

Stroke alarm-Arterial ischemic stroke as one of the most time-critical emergencies in children and adolescents

Motivational effects of top-rope climbing therapy under individualized prophylaxis: a pilot study in young adults with severe haemophilia

Prospects for research in haemophilia with real‐world data—An analysis of German registry and secondary data

The EPIC study: a lesson to learn

Aspirin versus low-dose low-molecular-weight heparin : Antithrombotic therapy in pediatric ischemic stroke patients : A prospective follow-up study

Blood coagulation disorders in children

Climbing therapy under PK-tailored prophylaxis

Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors

Repeated coagulation testing in children. Does it improve the diagnostic value?

Continuous infusion of factor concentrates in children with haemophilia A in comparison with bolus injections

Treatment of children with severe haemophilia A and inhibitors: a health economic evaluation for Germany

Immune tolerance induction with a factor VIII concentrate containing von Willebrand factor (Haemoctin SDH®) in 14 patients with severe haemophilia A

Notfall-Neuropädiatrie – Der arteriell ischämische Schlaganfall als einer der zeitkritischsten Notfälle bei Kindern und Jugendlichen

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

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