Britta A. P. Laros‐van Gorkom

Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A

Corien L. Eckhardt, Alice S. van Velzen, Marjolein Peters et al. · Blood · 2013 · 215 citations · Full text

Medicine, Genetics, Hematology +16

A Dominant-Negative <i>GFI1B</i> Mutation in the Gray Platelet Syndrome

Davide Monteferrario, Nikhita Bolar, Anna E. Marneth et al. · New England Journal of Medicine · 2013 · 164 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Determinants of bleeding phenotype in adult patients with moderate or severe von Willebrand disease

Eva M. de Wee, Yvonne Sanders, Eveline P. Mauser‐Bunschoten et al. · Thrombosis and Haemostasis · 2012 · 116 citations · Full text

Medicine, Hematology, Pathology +17

Health‐related quality of life among adult patients with moderate and severe von Willebrand disease

Eva M. de Wee, E. P. Mauser‐Bunschoten, Johanna G. van der Bom et al. · Journal of Thrombosis and Haemostasis · 2010 · 109 citations

Pharmacy, Internal Medicine, Health Assessment +11

von Willebrand disease and aging: an evolving phenotype

Yvonne Sanders, M.A. Giezenaar, Britta A. P. Laros‐van Gorkom et al. · Journal of Thrombosis and Haemostasis · 2014 · 107 citations · Full text

Life Sciences, Genetics, Pathology +10