Hans‐Hermann Brackmann

Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.

Jéfferson Becker, R. Schwaab, A. Möller-Taube et al. · PubMed · 1996 · 147 citations

Medicine, Genetics, Hematology +14

Prevalence and outcome of intracranial haemorrhage in haemophiliacs – a survey of the paediatric group of the German Society of Thrombosis and Haemostasis (GTH)

J. Klinge, K. Auberger, G. Auerswald et al. · European Journal of Pediatrics · 1999 · 127 citations

Medicine, Hematology, Pediatrics +14

Treatment of acquired hemophilia by the Bonn-Malmo Protocol: documentation of an in vivo immunomodulating concept

Heike Zeitler, G Ulrich‐Merzenich, Eligius Konsek et al. · Blood · 2004 · 119 citations · Full text

Medicine, Hematology, Immunology +11

Congenital Deficiency of Vitamin K Dependent Coagulation Factors in Two Families Presents as a Genetic Defect of the Vitamin K-Epoxide-Reductase-Complex

Benigna von Brederlow, Andreas Fregin, Simone Rost et al. · Thrombosis and Haemostasis · 2000 · 105 citations

Medicine, Genetics, Molecular Genetics +17

Missense mutations at ALA‐10 in the factor IX propeptide: an insignificant variant in normal life but a decisive cause of bleeding during oral anticoagulant therapy

Johannes Oldenburg, Ernst‐Markus Quenzel, Uschi Harbrecht et al. · British Journal of Haematology · 1997 · 97 citations · Full text

Medicine, Hematology, Pharmacology +14