K. Wulff

Hereditary angioedema with a mutation in the plasminogen gene

Konrad Bork, K. Wulff, Lars Steinmüller‐Magin et al. · Allergy · 2017 · 306 citations

Life Sciences, Genetics, Molecular Genetics +14

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Guglielmo Mariani, Falko H. Herrmann, Alberto Dolce et al. · Thrombosis and Haemostasis · 2005 · 257 citations

Medicine, Genetics, Hematology +17

Hereditary angioedema caused by missense mutations in the factor XII gene: Clinical features, trigger factors, and therapy

Konrad Bork, K. Wulff, Jochen Hardt et al. · Journal of Allergy and Clinical Immunology · 2009 · 203 citations

Medicine, Genetics, Molecular Genetics +10

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

F. H. Herrmann, G. Auerswald, Arlette Ruiz‐Sàez et al. · Haemophilia · 2006 · 196 citations

Medicine, Genetics, Molecular Genetics +17

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

F. H. Herrmann, K. Wulff, Günter Auerswald et al. · Haemophilia · 2009 · 151 citations

Medicine, Genetics, Molecular Genetics +17