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Over ons Praktische zaken Waar vindt u ons R.Y.J. Tamminga

Publicaties

Disease characteristics and outcomes of acute myeloid leukemia in germline RUNX1 deficiency (Familial Platelet Disorder with associated Myeloid Malignancy)

Genetic variants, thrombocytopenia, and clinical phenotype of type 2B von Willebrand disease: a median 16-year follow-up study

Occurrence of FVIII Inhibitors in Hemophilia A Patients Following an Institutional Switch to a Third Generation B-Domain-Deleted FVIII

Desmopressin testing in von Willebrand disease: Lowering the burden

A boy with joint pain associated with emicizumab treatment: The importance of plasma level measurement

Bleeding phenotype and diagnostic characterization of patients with congenital platelet defects

Congenital platelet disorders and health status-related quality of life

Flow cytometric mepacrine fluorescence can be used for the exclusion of platelet dense granule deficiency

One piece of the puzzle: Population pharmacokinetics of FVIII during perioperative Haemate P (R)/Humate P (R) treatment in von Willebrand disease patients

The Dutch Haemophilia Registry HemoNED - Building an ecosystem

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