Esmée Oussoren

Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor

Saskia B. Wortmann, Johan L.K. Van Hove, Terry G. J. Derks et al. · Blood · 2020 · 180 citations · Full text

Life Sciences, Pharmacology, Pharmacotherapy +10

Genes differentially expressed in medulloblastoma and fetal brain

Erna Michiels, Esmée Oussoren, Marjon van Groenigen et al. · Physiological Genomics · 1999 · 90 citations · Full text

Medicine, Developmental Biology, Oncology +16

Mucopolysaccharidosis: Cardiologic features and effects of enzyme‐replacement therapy in 24 children with MPS I, II and VI

Marion M. Brands, Ingrid M.E. Frohn-Mulder, M.L.C. Hagemans et al. · Journal of Inherited Metabolic Disease · 2012 · 71 citations · Full text

Medicine, Cardiology, Pediatrics +7

Genetic basis of alpha‐aminoadipic and alpha‐ketoadipic aciduria

Jacob Hagen, Heleen te Brinke, Ronald J. A. Wanders et al. · Journal of Inherited Metabolic Disease · 2015 · 59 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Residual α-l-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients

Esmée Oussoren, J. L. M. Keulemans, Otto P. van Diggelen et al. · Molecular Genetics and Metabolism · 2013 · 51 citations · Full text

Life Sciences, Pathology, Molecular Pathology +6