Tom J. de Koning
Department of Metabolic Diseases
University Children's Hospital Het Wilhelmina Kinderziekenhuis
Utrecht
Netherlands
Name/email consistency: high
- Serine-deficiency syndromes. de Koning, T.J., Klomp, L.W. Curr. Opin. Neurol. (2004)
- Prenatal and early postnatal treatment in 3-phosphoglycerate-dehydrogenase deficiency. de Koning, T.J., Klomp, L.W., van Oppen, A.C., Beemer, F.A., Dorland, L., van den Berg, I., Berger, R. Lancet (2004)
- L-serine in disease and development. de Koning, T.J., Snell, K., Duran, M., Berger, R., Poll-The, B.T., Surtees, R. Biochem. J. (2003)
- Congenital microcephaly and seizures due to 3-phosphoglycerate dehydrogenase deficiency: outcome of treatment with amino acids. De Koning, T.J., Duran, M., Van Maldergem, L., Pineda, M., Dorland, L., Gooskens, R., Jaeken, J., Poll-The, B.T. J. Inherit. Metab. Dis. (2002)
- Congenital hepatic fibrosis in 3 siblings with phosphomannose isomerase deficiency. de Koning, T.J., Nikkels, P.G., Dorland, L., Bekhof, J., De Schrijver, J.E., van Hattum, J., van Diggelen, O.P., Duran, M., Berger, R., Poll-The, B.T. Virchows Arch. (2000)
- Hypomyelination and reversible white matter attenuation in 3-phosphoglycerate dehydrogenase deficiency. de Koning, T.J., Jaeken, J., Pineda, M., Van Maldergem, L., Poll-The, B.T., van der Knaap, M.S. Neuropediatrics (2000)
