Inherited platelet disorders
NURDEN, A. T., FRESON, K., SELIGSOHN, U.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2012)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2012)
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Review article: blood platelet number and function in chronic liver disease and cirrhosis
WITTERS, P., FRESON, K., VERSLYPE, C., PEERLINCK, K., HOYLAERTS, M., NEVENS, F., VAN GEET, C., CASSIMAN, D.
Published in Alimentary pharmacology & therapeutics (01.06.2008)
Published in Alimentary pharmacology & therapeutics (01.06.2008)
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Regulators of G protein signaling: role in hematopoiesis, megakaryopoiesis and platelet function
LOUWETTE, S., VAN GEET, C., FRESON, K.
Published in Journal of thrombosis and haemostasis (01.11.2012)
Published in Journal of thrombosis and haemostasis (01.11.2012)
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DNA methylation in imprinted genes IGF2 and GNASXL is associated with prenatal maternal stress
Vangeel, E. B., Izzi, B., Hompes, T., Vansteelandt, K., Lambrechts, D., Freson, K., Claes, S.
Published in Genes, brain and behavior (01.11.2015)
Published in Genes, brain and behavior (01.11.2015)
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Regulators of platelet cAMP levels: clinical and therapeutic implications
Noé, L, Peeters, K, Izzi, B, Van Geet, C, Freson, K
Published in Current medicinal chemistry (01.09.2010)
Published in Current medicinal chemistry (01.09.2010)
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A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder
HERMANS, C., WITTEVRONGEL, C., THYS, C., SMETHURST, P. A., VAN GEET, C., FRESON, K.
Published in Journal of thrombosis and haemostasis (01.08.2009)
Published in Journal of thrombosis and haemostasis (01.08.2009)
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Update on the causes of platelet disorders and functional consequences
Freson, K., Wijgaerts, A., van Geet, C.
Published in International journal of laboratory hematology (01.06.2014)
Published in International journal of laboratory hematology (01.06.2014)
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Pituitary adenylate cyclase‐activating polypeptide deficiency associated with increased platelet count and aggregability in nephrotic syndrome
Eneman, B., Freson, K., Heuvel, L., hoyweghen, E., Collard, L., Vande Walle, J., Geet, C., Levtchenko, E.
Published in Journal of thrombosis and haemostasis (01.05.2015)
Published in Journal of thrombosis and haemostasis (01.05.2015)
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The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG‐Arg301 to be distinguished from hypofibrinogenemia
Jacquemin, M., Vanlinthout, I., Van Horenbeeck, I., Debasse, M., Toelen, J., Schoeters, J., Lavend'homme, R., Freson, K., Peerlinck, K.
Published in International journal of laboratory hematology (01.06.2017)
Published in International journal of laboratory hematology (01.06.2017)
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Human platelet pathology related to defects in the G‐protein signaling cascade
VAN GEET, C., IZZI, B., LABARQUE, V., FRESON, K.
Published in Journal of thrombosis and haemostasis (01.07.2009)
Published in Journal of thrombosis and haemostasis (01.07.2009)
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Platelet Gs hypofunction and abnormal morphology resulting from a heterozygous RGS2 mutation
NOÉ, L., DI MICHELE, M., GIETS, E., THYS, C., WITTEVRONGEL, C., DE VOS, R., OVERBERGH, L., WAELKENS, E., JAEKEN, J., VAN GEET, C., FRESON, K.
Published in Journal of thrombosis and haemostasis (01.07.2010)
Published in Journal of thrombosis and haemostasis (01.07.2010)
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The effect of paternal methyl-group donor intake on offspring DNA methylation and birth weight
Pauwels, S., Truijen, I., Ghosh, M., Duca, R. C., Langie, S. A. S., Bekaert, B., Freson, K., Huybrechts, I., Koppen, G., Devlieger, R., Godderis, L.
Published in Journal of developmental origins of health and disease (01.06.2017)
Published in Journal of developmental origins of health and disease (01.06.2017)
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Proteomic analysis of platelet N -glycoproteins in PMM2-CDG patients
de la Morena-Barrio, M.E, Di Michele, M, Lozano, M.L, Rivera, J, Pérez-Dueñas, B, Altisent, C, Sevivas, T, Vicente, V, Jaeken, J, Freson, K, Corral, J
Published in Thrombosis research (01.03.2014)
Published in Thrombosis research (01.03.2014)
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Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation
FRESON, Kathleen, MATTHIJS, Gert, THYS, Chantal, MARIËN, Paul, HOYLAERTS, Marc F, VERMYLEN, Jos, VAN GEET, Chris
Published in Human molecular genetics (15.01.2002)
Published in Human molecular genetics (15.01.2002)
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ADP‐degrading enzymes inhibit platelet activation in bile duct‐ligated rats
WITTERS, P., HOYLAERTS, M., FRESON, K., DE VOS, R., VAN PELT, J., NEVENS, F., VAN GEET, C., CASSIMAN, D.
Published in Journal of thrombosis and haemostasis (01.02.2010)
Published in Journal of thrombosis and haemostasis (01.02.2010)
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