Selene C. M. Schoormans

Importance of Genotyping in von Willebrand Disease to Elucidate Pathogenic Mechanisms and Variability in Phenotype

Ferdows Atiq, Johan Boender, Waander L. van Heerde et al. · HemaSphere · 2022 · 21 citations · Full text

The hypolipidemic action of bezafibrate therapy in hypertriglyceridemia is mediated by upregulation of lipoprotein lipase: no effects on VLDL substrate affinity to lipolysis or LDL receptor binding

Frits H.A.F. de Man, Femke de Beer, Arnoud van der Laarse et al. · Atherosclerosis · 2000 · 20 citations

Lipoprotein Lipase, Metabolic Syndrome, Thrombosis +14

Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype

M. E. R. van Meegeren, Tiziano Mancini, Selene C. M. Schoormans et al. · Haemophilia · 2015 · 19 citations · Full text

Thirteen novel mutations in the <i>factor VIII</i> gene in the Nijmegen haemophilia A patient population

J. C. A. Boekhorst, Bert Verbruggen, Jean Maurice Lavergne et al. · British Journal of Haematology · 2005 · 17 citations · Full text

Von Willebrand disease type 2M: Correlation between genotype and phenotype

Dominique P.M.S.M. Maas, Ferdows Atiq, Nicole M. A. Blijlevens et al. · Journal of Thrombosis and Haemostasis · 2021 · 17 citations · Full text

Mendelian Disorder, Disease Mechanism, Genetic Disorder +8