Marjon H. Cnossen
Marjon H. Cnossen
Erasmus MC-Sophia Children's Hospital, OPTI-CLOT, SCORE, CRESCENDO/ DoReMI, WiN, INSIGHT
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Cited by
Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A
CL Eckhardt, AS Van Velzen, M Peters, J Astermark, PP Brons, ...
Blood, The Journal of the American Society of Hematology 122 (11), 1954-1962, 2013
A prospective 10 year follow up study of patients with neurofibromatosis type 1
MH Cnossen, A de Goede-Bolder, KM Van den Broek, CME Waasdorp, ...
Archives of disease in childhood 78 (5), 408-412, 1998
Diagnosis and management of haemophilia
K Fijnvandraat, MH Cnossen, FWG Leebeek, M Peters
Bmj 344, 2012
Age dependency of coagulation parameters during childhood and puberty
IM Appel, B Grimminck, J Geerts, R Stigter, MH Cnossen, A Beishuizen
Journal of Thrombosis and Haemostasis 10 (11), 2254-2263, 2012
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype‐phenotype correlations in neurofibromatosis type 1?
MH Cnossen, MN van der Est, MH Breuning, CJ van Asperen, ...
Human mutation 9 (5), 458-464, 1997
von Willebrand disease and aging: an evolving phenotype
YV Sanders, MA Giezenaar, BAP Laros‐van Gorkom, K Meijer, ...
Journal of Thrombosis and Haemostasis 12 (7), 1066-1075, 2014
Paediatric arterial ischaemic stroke: functional outcome and risk factors
MH Cnossen, FK Aarsen, SLJVANDEN AKKER, R Danen, IM Appel, ...
Developmental Medicine & Child Neurology 52 (4), 394-399, 2010
Reduced prevalence of arterial thrombosis in von Willebrand disease
YV Sanders, J Eikenboom, EM de Wee, JG van der Bom, MH Cnossen, ...
Journal of Thrombosis and Haemostasis 11 (5), 845-854, 2013
Endocrinologic disorders and optic pathway gliomas in children with neurofibromatosis type 1
MH Cnossen, EN Stam, LCMG Cooiman, HJ Simonsz, H Stroink, ...
Pediatrics 100 (4), 667-670, 1997
von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease
YV Sanders, D Groeneveld, K Meijer, K Fijnvandraat, MH Cnossen, ...
Blood, The Journal of the American Society of Hematology 125 (19), 3006-3013, 2015
Side effects of desmopressin in patients with bleeding disorders
SCM Stoof, MH Cnossen, MPM De Maat, FWG Leebeek, M Kruip
Haemophilia 22 (1), 39-45, 2016
Inhibitor development and mortality in non‐severe hemophilia A
CL Eckhardt, JI Loomans, AS Van Velzen, M Peters, ...
Journal of Thrombosis and Haemostasis 13 (7), 1217-1225, 2015
Volume of white matter hyperintensities is an independent predictor of intelligence quotient and processing speed in children with sickle cell disease
V van der Land, CT Hijmans, M de Ruiter, HJMM Mutsaerts, MH Cnossen, ...
British journal of haematology 168 (4), 553-556, 2015
Sickle cell disease: clinical presentation and management of a global health challenge
ME Houwing, PJ De Pagter, EJ Van Beers, BJ Biemond, E Rettenbacher, ...
Blood reviews 37, 100580, 2019
Early occurrence of red blood cell alloimmunization in patients with sickle cell disease
JWR Sins, BJ Biemond, SM van den Bersselaar, H Heijboer, ...
American journal of hematology 91 (8), 763-769, 2016
Adherence to prophylaxis and bleeding outcome in haemophilia: a multicentre study
LSH Schrijvers, M Beijlevelt‐van der Zande, M Peters, J Lock, ...
British Journal of Haematology 174 (3), 454-460, 2016
Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients
MAE Rab, BA van Oirschot, J Bos, TH Merkx, ACW van Wesel, ...
American journal of hematology 94 (5), 575-584, 2019
Minor disease features in neurofibromatosis type 1 (NF1) and their possible value in diagnosis of NF1 in children< or= 6 years and clinically suspected of having NF1 …
MH Cnossen, KG Moons, MP Garssen, NM Pasmans, A de Goede-Bolder, ...
Journal of medical genetics 35 (8), 624-627, 1998
Bleeding spectrum in children with moderate or severe von W illebrand disease: R elevance of pediatric‐specific bleeding
YV Sanders, K Fijnvandraat, J Boender, EP Mauser‐Bunschoten, ...
American Journal of Hematology 90 (12), 1142-1148, 2015
Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications
H Hazendonk, J Lock, RAA Mathôt, K Meijer, M Peters, ...
Journal of Thrombosis and Haemostasis 14 (3), 468-478, 2016
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