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Journal of Thrombosis and Haemostasis : JTH|June 26, 2009
A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorderC Hermans, C Wittevrongel, C Thys, et al.Human Mutation|May 29, 1998
Fluorescent chemical cleavage of mismatches for efficient screening of the factor VIII geneK Freson, K Peerlinck, T Aguirre, et al.Genes, Brain, and Behavior|September 4, 2015
DNA methylation in imprinted genes IGF2 and GNASXL is associated with prenatal maternal stressE B Vangeel, B Izzi, T Hompes, et al.Thrombosis and Haemostasis|October 5, 2001
Genetic variation of the extra-large stimulatory G protein alpha-subunit leads to Gs hyperfunction in platelets and is a risk factor for bleedingK Freson, M F Hoylaerts, J Jaeken, et al.Journal of Inherited Metabolic Disease|October 13, 2001
Congenital disorders of glycosylation type Ia and IIa are associated with different primary haemostatic complicationsC Van Geet, J Jaeken, K Freson, et al.Alimentary Pharmacology & Therapeutics|March 12, 2008
Review article: blood platelet number and function in chronic liver disease and cirrhosisP Witters, K Freson, C Verslype, et al.Journal of Thrombosis and Haemostasis : JTH|November 10, 2009
ADP-degrading enzymes inhibit platelet activation in bile duct-ligated ratsP Witters, M Hoylaerts, K Freson, et al.International Journal of Laboratory Hematology|March 21, 2017
The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemiaM Jacquemin, I Vanlinthout, I Van Horenbeeck, et al.Journal of Thrombosis and Haemostasis : JTH|March 12, 2015
Pituitary adenylate cyclase-activating polypeptide deficiency associated with increased platelet count and aggregability in nephrotic syndromeB Eneman, K Freson, L van den Heuvel, et al.Blood|June 22, 2001
Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutationK Freson, K Devriendt, G Matthijs, et al.Pageof 3