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(1 - 9 of 9)
Thrombocytopenia in neonatal sepsis: Incidence, severity and risk factors
Ree, I.M.C.; Fustolo-Gunnink, S.F.; Bekker, V.; Fijnvandraat, K.J.; Steggerda, S.J.; Lopriore, E. 2017
Thrombocytopenia in neonatal sepsis: Incidence, severity and risk factors
Article / Letter to editor
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In Vivo Ti of Blood Measurements in Children with Sickle Cell Disease Improve Cerebral Blood Flow Quantification from Arterial Spin-Labeling MRI
Vaclavu, L.; Land, V. van der; Heijtel, D.F.R.; Osch, M.J.P. van; Cnossen, M.H.; Majoie, C.B.L.M.; ... ; Nederveen, A.J. 2016
In Vivo Ti of Blood Measurements in Children with Sickle Cell Disease Improve Cerebral Blood Flow Quantification from Arterial Spin-Labeling MRI
Article / Letter to editor
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Genetic variations determine von Willebrand factor levels in patients with von Willebrand disease from the WiN study
Sanders, Y.V.; Bom, J.G. van der; Cnossen, M.H.; Maat, P.M. de; Laros-van Gorkom, B.A.P.; Fijnvandraat, K.J.; ... ; Leebeek, F.W.G. 2013
Genetic variations determine von Willebrand factor levels in patients with von Willebrand disease from the WiN study
Article / Letter to editor
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Factor VIII gene (F8) mutation and inhibitor development in non-severe hemophilia A
Groot-Eckhardt, C.L. de; Velzen, A.S. van; Peters, M.; Peerlinck, K.; Oldenburg, J.; Santagostino, E.; ... ; INSIGHT Consortium 2013
Factor VIII gene (F8) mutation and inhibitor development in non-severe hemophilia A
Article / Letter to editor
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Hemophilia arthropathy occurs in a significant percentage in von Willebrands disease
Galen, K.P.M. van; Sanders, Y.V.; Schaefer, T.M.; Eikenboom, H.C.J.; Bom, J.G. van der; Fijnvandraat, K.J.; ... ; Mauser-Bunschoten, E. 2013
Hemophilia arthropathy occurs in a significant percentage in von Willebrands disease
Article / Letter to editor
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RISE- response to DDAVP in moderate/mild haemophilia A patients: in search for determinants
Loomans, J.I.; Velzen, A.S. van; Kruip, J.H.A.; Santagostino, E.; Eckhardt, C.L.; Castaman, G.; ... ; Fijnvandraat, K.J. 2013
RISE- response to DDAVP in moderate/mild haemophilia A patients: in search for determinants
Article / Letter to editor
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Inhibitor eradication therapy in non-severe hemophilia A
Velzen, A.S. van; Eckhardt, C.L.; Peters, M.; Hart, P.; Rangarajan, S.; Hay, C.R.M.; ... ; INSIGHT Consortium 2013
Inhibitor eradication therapy in non-severe hemophilia A
Article / Letter to editor
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Clinical risk factors in the development of inhibitors in non-severe hemophilia A patients: the first results of the INSIGHT case-control study
Velzen, A.S. van; Eckhardt, C.L.; Peters, M.; Peerlinck, K.; Oldenburg, J.; Hay, C.R.M.; ... ; Fijnvandraat, K.J. 2013
Clinical risk factors in the development of inhibitors in non-severe hemophilia A patients: the first results of the INSIGHT case-control study
Article / Letter to editor
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Iatrogenic bleeding is the presenting symptom in children with moderate or severe von Willebrand disease - from the WiN study
Sanders, Y.V.; Fijnvandraat, K.J.; Mauser-Bunschoten, E.; Bom, J.G. van der; Meris, J. de; Eikenboom, H.C.J.; ... ; Leebeek, F.W.G. 2013
Iatrogenic bleeding is the presenting symptom in children with moderate or severe von Willebrand disease - from the WiN study
Article / Letter to editor
metadata only