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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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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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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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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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Hämostaseologie in der Pädiatrie

Hämostaseologie, 2008, Vol.28 (5), p.465-471

Kurnik, K.

2008

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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 (S 01), p.S13-S16

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.218-200

2001

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Hämostaseologie in der Pädiatrie

Hämostaseologie, 2004, Vol.24 (2), p.116-122

Kurnik, K.

2004

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

Hämostaseologie, 2011-11, Vol.31 Suppl 1 (S 01), p.S51-S56

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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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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Meeting Report: Ninth and Tenth Workshops of the European Paediatric Network for Haemophilia Management (PedNet)

Haemophilia, 2007-09, Vol.13 (5), p.658-662

2007

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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

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

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

The EPIC study: a lesson to learn

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

Hämostaseologie in der Pädiatrie

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

Hämostaseologie in der Pädiatrie

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

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

Meeting Report: Ninth and Tenth Workshops of the European Paediatric Network for Haemophilia Management (PedNet)

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