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Auswirkungen der COVID-19 Pandemie auf die medizinische Versorgung von Patienten mit angeborenen Blutungsneigungen

Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)), 2021-04, Vol.83 (4), p.282-290

2021

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Smart Medication ™, an Electronic Diary for Surveillance of Haemophilia Home Care and Optimization of Resource Distribution

Hämostaseologie, 2019-11, Vol.39 (4), p.339-346

2019

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Early orthopaedic challenges in haemophilia patients and therapeutic approach

Thrombosis research, 2014-11, Vol.134, p.S61-S67

2014

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Impact of COVID‐19 pandemic on mental health of patients with inherited bleeding disorders in Germany

Haemophilia : the official journal of the World Federation of Hemophilia, 2020-11, Vol.26 (6), p.e272-e281

2020

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Impact of COVID-19 Pandemic on Medical Care of Patients with Inherited Bleeding Disorders

Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)), 2021-04, Vol.83 (4), p.282

2021

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Popliteal venous thrombosis in juvenile arthritis with Baker cysts: report of 3 cases

Pediatric rheumatology online journal, 2008-07, Vol.6 (1), p.12-12, Article 12

2008

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Practical Guidance of the GTH Haemophilia Board on the Use of Emicizumab in Patients with Haemophilia A

Hamostaseologie, 2020-12, Vol.40 (5), p.561-571

2020

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Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia

Thrombosis and haemostasis, 2001-12, Vol.86 (6), p.1360-1362

2001

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The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF

Blood, 2010-06, Vol.115 (22), p.4580-4587

2010

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Management Of Pregnancy In Patients With Antithrombin Deficiency

Blood, 2013-11, Vol.122 (21), p.216-216

2013

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Addition of in-vitro generated endothelial microparticles to von-Willebrand plasma improves primary and secondary hemostasis

Thrombosis research, 2014-03, Vol.133 (3), p.445-450

2014

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Prospective Evaluation of the Thrombotic Risk in Children With Acute Lymphoblastic Leukemia Carrying the MTHFR TT 677 Genotype, the Prothrombin G20210A Variant, and Further Prothrombotic Risk Factors

Blood, 1999-03, Vol.93 (5), p.1595-1599

1999

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Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A

Human mutation, 2007-01, Vol.28 (1), p.54-60

2007

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Wozu bezahlt man denn Krankenkasse, wenn man, sage ich 'mal, nichts rauskriegt??" Qualitative Studie zum Verständnis von Solidarität in der GKV im Kontext der Priorisierungsdebatte

Sozialer Fortschritt (Berlin), 2011-04, Vol.60 (4-5), p.73-81

2011

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Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors

Blood, 1999-03, Vol.93 (5), p.1595-1599

1999

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Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

Human mutation, 2005-09, Vol.26 (3), p.249-254

2005

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MYH9-related disease: Report on five German families and description of a novel mutation

Annals of hematology, 2010-10, Vol.89 (10), p.1057-1059

2010

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The deletion polymorphism in the angiotensin-converting enzyme gene is a moderate risk factor for venous thromboembolism

Thrombosis and haemostasis, 2003-05, Vol.89 (5), p.847-852

2003

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A Novel Mutation in the von Willebrand Factor Propeptide Causes Defective Regulated Storage in Platelets and Weibel-Palade Bodies

Blood, 2005-11, Vol.106 (11), p.1007-1007

2005

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Wozu bezahlt man denn Krankenkasse, wenn man, sage ich 'mal, nichts rauskriegt?

Sozialer Fortschritt (Berlin), 2011-04, Vol.60 (4–5), p.73-81

2011

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Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)

Thrombosis research, 2002, Vol.105 (1), p.49-53

2002

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Retention test homburg to monitor the adhesive properties of von willebrand factor after substitution or desmopressin therapy: Reliability of platelet function tests and drug monitoring

Seminars in thrombosis and hemostasis, 2005, Vol.31 (4), p.441-448

2005

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Retention Test Homburg To Monitor the Adhesive Properties of von Willebrand Factor after Substitution or Desmopressin Therapy

Seminars in thrombosis and hemostasis, 2005-08, Vol.31 (4), p.441-448

2005

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Smart Medication ™, an Electronic Diary for Surveillance of Haemophilia Home Care and Optimization of Resource Distribution

Hamostaseologie, 2019-11, Vol.39 (4), p.339

2019

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Auswirkungen der COVID-19 Pandemie auf die medizinische Versorgung von Patienten mit angeborenen Blutungsneigungen

Smart Medication ™, an Electronic Diary for Surveillance of Haemophilia Home Care and Optimization of Resource Distribution

Early orthopaedic challenges in haemophilia patients and therapeutic approach

Impact of COVID‐19 pandemic on mental health of patients with inherited bleeding disorders in Germany

Impact of COVID-19 Pandemic on Medical Care of Patients with Inherited Bleeding Disorders

Popliteal venous thrombosis in juvenile arthritis with Baker cysts: report of 3 cases

Practical Guidance of the GTH Haemophilia Board on the Use of Emicizumab in Patients with Haemophilia A

Prevalence of a 23bp insertion in exon 3 of the endothelial cell protein C receptor gene in venous thrombophilia

The mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF

Management Of Pregnancy In Patients With Antithrombin Deficiency

Addition of in-vitro generated endothelial microparticles to von-Willebrand plasma improves primary and secondary hemostasis

Prospective Evaluation of the Thrombotic Risk in Children With Acute Lymphoblastic Leukemia Carrying the MTHFR TT 677 Genotype, the Prothrombin G20210A Variant, and Further Prothrombotic Risk Factors

Spectrum of molecular defects and mutation detection rate in patients with mild and moderate hemophilia A

Wozu bezahlt man denn Krankenkasse, wenn man, sage ich 'mal, nichts rauskriegt??" Qualitative Studie zum Verständnis von Solidarität in der GKV im Kontext der Priorisierungsdebatte

Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors

Spectrum of molecular defects and mutation detection rate in patients with severe hemophilia A

MYH9-related disease: Report on five German families and description of a novel mutation

The deletion polymorphism in the angiotensin-converting enzyme gene is a moderate risk factor for venous thromboembolism

A Novel Mutation in the von Willebrand Factor Propeptide Causes Defective Regulated Storage in Platelets and Weibel-Palade Bodies

Wozu bezahlt man denn Krankenkasse, wenn man, sage ich 'mal, nichts rauskriegt?

Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)

Retention test homburg to monitor the adhesive properties of von willebrand factor after substitution or desmopressin therapy: Reliability of platelet function tests and drug monitoring

Retention Test Homburg To Monitor the Adhesive Properties of von Willebrand Factor after Substitution or Desmopressin Therapy

Smart Medication ™, an Electronic Diary for Surveillance of Haemophilia Home Care and Optimization of Resource Distribution

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