T.g.j. (terry) Derks
consultant pediatric metabolic diseases
Medical Sciences
University of Groningen
Netherlands
Biography
T.G.J. (Terry) Derks, consultant pediatric metabolic diseases, Faculty of Medical Sciences Paediatrics: Paediatrics, Hanzeplein 1, 9713 GZ Groningen, The Netherlands.
Research Interest
Genetics & Heredity, Pediatrics, Nutrition & Dietetics
Publications
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van Rijt, W. J., Jager, E. A., Spronsen, van, F. J., de Koning, T., Heiner-Fokkema, M. R., & Derks, T. G. J. (2016). Neonates at risk of medium-chain acyl-CoA dehydrogenase deficiency: a perinatal protocol for use before population neonatal screening test results become available. Genetics in Medicine, 18(12), 1322-1323. DOI: 10.1038/gim.2016.149
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van Dam, E., Daly, A., Venema-Liefaard, G., van Rijn, M., Derks, T. G. J., McKiernan, P. J., ... van Spronsen, F. J. (2017). What Is the Best Blood Sampling Time for Metabolic Control of Phenylalanine and Tyrosine Concentrations in Tyrosinemia Type 1 Patients? Journal of Inherited Metabolic Disorders, 1-9. DOI: 10.1007/8904_2016_37
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Lawrence, N. T., Chengsupanimit, T., Brown, L. M., Derks, T. G. J., Smit, G. P. A., & Weinstein, D. A. (2017). Inflammatory Bowel Disease in Glycogen Storage Disease Type Ia: A Case Series. Journal of Pediatric Gastroenterology and Nutrition, 64(2), 52-54. DOI: 10.1097/MPG.0000000000000592
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Hijmans, B. S., Boss, A., van Dijk, T. H., Soty, M., Wolters, H., Mutel, E., ... Oosterveer, M. H. (2017). Hepatocytes contribute to residual glucose production in a mouse model for glycogen storage disease type Ia. Hepatology. DOI: 10.1002/hep.29389