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Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

Journal of thrombosis and haemostasis, 2012-04, Vol.10 (4), p.615-621

2012

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PBAC score: an easy-to-use tool to predict coagulation disorders in women with idiopathic heavy menstrual bleeding

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-05, Vol.22 (3), p.e217-e220

2016

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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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Women with inherited bleeding disorders - experience as an affected woman and as a treating doctor

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-07, Vol.17 (s1), p.31-32

HALIMEH, S.

2011

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Menorrhagia and bleeding disorders in adolescent females

Hämostaseologie, 2012, Vol.32 (1), p.45-50

Halimeh, S

2012

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Pharmacokinetics of recombinant factor XIII at steady state in patients with congenital factor XIII A‐subunit deficiency

Journal of thrombosis and haemostasis, 2014-12, Vol.12 (12), p.2038-2043

2014

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P-053: Establishing reference ranges for coagulation parameters during pregnancy

Thrombosis research, 2017-03, Vol.151, p.S125-S126

2017

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New recommendations on cerebral venous and dural sinus thrombosis from the German consensus-based (S2k) guideline

Neurological research and practice, 2024-04, Vol.6 (1), p.23-23, Article 23

2024

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Petrography and geochemistry of Paleocene-Eocene limestones in the Ching-dar syncline, eastern Iran

Di xue qian yuan., 2014-05, Vol.5 (3), p.429-438

2014

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OC-11 Is a PBAC-score a good tool to quantify menorrhagia in women with von Willebrand disease and rare bleeding disorders?

Thrombosis research, 2013, Vol.131, p.S73-S74

2013

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How fit are children and adolescents with haemophilia in Germany? Results of a prospective study assessing the sport-specific motor performance by means of modern test procedures of sports science

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.523-529

2015

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Results of the WIRK prospective, non-interventional observational study of recombinant activated factor VII (rFVIIa) in patients with congenital haemophilia with inhibitors and other bleeding disorders

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-09, Vol.19 (5), p.679-685

2013

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Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

Haematologica (Roma), 2010-06, Vol.95 (6), p.956-962

2010

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P-072 Recurrent spontaneous abortion in women with bleeding disorders

Thrombosis research, 2013, Vol.131, p.S95-S95

2013

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P-071 The PBAC score is an easy tool to quantity menstrual blood loss in women

Thrombosis research, 2013, Vol.131, p.S95-S95

2013

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PB0648 Mitigating the Risk of Bleeds and the Risk for Inhibitor Formation when Treating Previously Untreated Patients (PUPs) with Severe Haemophilia A - A Single-Centre Approach

Research and practice in thrombosis and haemostasis, 2023-10, Vol.7, p.101188, Article 101188

2023

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Management of bleeding disorders in children

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (s2), p.15-23

2012

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Successful Allogenic Haematopoietic Stem Cell Transplantation in a Boy with Hemophilia A and MDS-RAEB

Klinische Padiatrie, 2016-11, Vol.228 (6-07), p.336

2016

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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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Patient preference and ease of use for different coagulation factor VIII reconstitution device scenarios: a cross-sectional survey in five European countries [Corrigendum]

Patient preference and adherence, 2015-01, Vol.9 (default), p.243-243

2015

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Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents

Klinische Padiatrie, 2010-05, Vol.222 (3), p.158

2010

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Treatment of haemophilia with an integrated therapeutical concept--Duisburg model

Hämostaseologie, 2012, Vol.32 Suppl 1, p.S25

2012

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Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families

Klinische Padiatrie, 2012-04, Vol.224 (3), p.174-178

2012

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Thrombolysis in newborns and infants

Thrombosis and haemostasis, 1999, Vol.82 Suppl 1 (S 01), p.112-116

1999

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Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

PBAC score: an easy-to-use tool to predict coagulation disorders in women with idiopathic heavy menstrual bleeding

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

Women with inherited bleeding disorders - experience as an affected woman and as a treating doctor

Menorrhagia and bleeding disorders in adolescent females

Pharmacokinetics of recombinant factor XIII at steady state in patients with congenital factor XIII A‐subunit deficiency

P-053: Establishing reference ranges for coagulation parameters during pregnancy

New recommendations on cerebral venous and dural sinus thrombosis from the German consensus-based (S2k) guideline

Petrography and geochemistry of Paleocene-Eocene limestones in the Ching-dar syncline, eastern Iran

OC-11 Is a PBAC-score a good tool to quantify menorrhagia in women with von Willebrand disease and rare bleeding disorders?

How fit are children and adolescents with haemophilia in Germany? Results of a prospective study assessing the sport-specific motor performance by means of modern test procedures of sports science

Results of the WIRK prospective, non-interventional observational study of recombinant activated factor VII (rFVIIa) in patients with congenital haemophilia with inhibitors and other bleeding disorders

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

P-072 Recurrent spontaneous abortion in women with bleeding disorders

P-071 The PBAC score is an easy tool to quantity menstrual blood loss in women

PB0648 Mitigating the Risk of Bleeds and the Risk for Inhibitor Formation when Treating Previously Untreated Patients (PUPs) with Severe Haemophilia A - A Single-Centre Approach

Management of bleeding disorders in children

Successful Allogenic Haematopoietic Stem Cell Transplantation in a Boy with Hemophilia A and MDS-RAEB

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

Patient preference and ease of use for different coagulation factor VIII reconstitution device scenarios: a cross-sectional survey in five European countries [Corrigendum]

Multiplate whole blood impedance point of care aggregometry: preliminary reference values in healthy infants, children and adolescents

Treatment of haemophilia with an integrated therapeutical concept--Duisburg model

Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families

Therapy of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)

Thrombolysis in newborns and infants

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