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Published in American journal of hematology (01.12.2016)
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The challenge of managing hemophilia A and STEC-induced hemolytic uremic syndrome
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An unusual cause of atrial tachycardia in a young patient with lymphoma
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Image Gallery: A rare abscess‐like presentation of Langerhans cell histiocytosis
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Clinical phenotype in genetically confirmed von Willebrand disease type 2N patients reflects a haemophilia A phenotype
van Meegeren, M. E. R., Mancini, T. L., Schoormans, S. C. M., van Haren, B. J. T., van Duren, C., Diekstra, A., Laros-van Gorkom, B. A. P., Brons, P. P. T., Simons, A., Hoefsloot, L., van Heerde, W. L.
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X-linked sideroblastic anaemia due to ALAS₂ mutations in the Netherlands: a disease in disguise
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Management of haemophilia in three premature infants
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Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.03.2008)
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Microcytic anaemia with low transferrin saturation, increased serum hepcidin and non‐synonymous TMPRSS 6 variants: not always iron‐refractory iron deficiency anaemia
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Published in British journal of haematology (01.04.2015)
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