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Pediatrics|October 2, 1997
Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1M H Cnossen, E N Stam, L C Cooiman, et al.Archives of Disease in Childhood|July 11, 1998
A prospective 10 year follow up study of patients with neurofibromatosis type 1M H Cnossen, A de Goede-Bolder, K M van den Broek, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 28, 2015
Facilitating the implementation of pharmacokinetic-guided dosing of prophylaxis in haemophilia care by discrete choice experimentJ Lock, E W de Bekker-Grob, G Urhan, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 25, 2018
Fifth Åland Island conference on von Willebrand diseaseE Berntorp, A Ågren, L Aledort, et al.Blood Reviews|May 27, 2019
Sickle cell disease: Clinical presentation and management of a global health challengeM E Houwing, P J de Pagter, E J van Beers, et al.AJNR. American Journal of Neuroradiology|May 28, 2016
In Vivo T1 of Blood Measurements in Children with Sickle Cell Disease Improve Cerebral Blood Flow Quantification from Arterial Spin-Labeling MRIL Václavů, V van der Land, D F R Heijtel, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 10, 2015
Joint surgery in von Willebrand disease: a multicentre cross-sectional studyK P M van Galen, K Meijer, H C Vogely, et al.Human Mutation|January 1, 1997
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?M H Cnossen, M N van der Est, M H Breuning, et al.Journal of Thrombosis and Haemostasis : JTH|December 30, 2015
Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complicationsH C A M Hazendonk, J Lock, R A A Mathôt, et al.Journal of Thrombosis and Haemostasis : JTH|April 23, 2014
von Willebrand disease and aging: an evolving phenotypeY V Sanders, M A Giezenaar, B A P Laros-van Gorkom, et al.Pageof 4