All Stories

  1. Understanding the functional difference between growth arrest-specific protein 6 and protein S: an evolutionary approach

    Article • Open Biology, October 2014, Royal Society Publishing

    Dr René Mulder, Romain A Studer, Professor Fred R. Opperdoes

  2. Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency

    Article • Thrombosis and Haemostasis, March 2013, Schattauer GmbH

    Dr René Mulder

  3. PROS1 Heerlen polymorphism is associated with increased free plasma tissue factor pathway inhibitor levels

    Article • Thrombosis and Haemostasis, January 2012, Schattauer GmbH

    Dr René Mulder

  4. The impact of antiproteinuric therapy on the prothrombotic state in patients with overt proteinuria

    Article • Journal of Thrombosis and Haemostasis, December 2011, Elsevier

    Dr René Mulder

  5. Decreased free protein S levels and venous thrombosis in the acute setting, a case-control study

    Article • Thrombosis Research, November 2011, Elsevier

    Dr René Mulder

  6. Relationship between cytomegalovirus infection and procoagulant changes in human immunodeficiency virus‐infected patients

    Article • Clinical Microbiology and Infection, May 2011, Elsevier

    Dr René Mulder

  7. Associations between high factor VIII and low free protein S levels with traditional arterial thrombotic risk factors and their risk on arterial thrombosis: Results from a retrospective family cohort study

    Article • Thrombosis Research, October 2010, Elsevier

    Dr René Mulder

  8. Low cut-off values increase diagnostic performance of protein S assays

    Article • Thrombosis and Haemostasis, June 2010, Schattauer GmbH

    Dr René Mulder

  9. Clinical relevance of decreased free protein S levels: results from a retrospective family cohort study involving 1143 relatives

    Article • Blood, February 2009, American Society of Hematology

    Dr René Mulder

  10. PROS1analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations

    Article • Human Mutation, July 2008, Hindawi Publishing Corporation

    Dr René Mulder