Tom J de Koning

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  1. Identification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymes

    Wouter F. Visser, Nanda M. Verhoeven-Duif & Tom J. De Koning, 2012 Jun 22, In: Journal of Biological Chemistry. 287, 26, p. 21654-21662

    Research output: Contribution to journalArticle

  2. A sensitive and simple ultra-high-performance-liquid chromatography-tandem mass spectrometry based method for the quantification of d-amino acids in body fluids

    Wouter F. Visser, Nanda M. Verhoeven-Duif, Roel Ophoff, Steven Bakker, Leo W. Klomp, Ruud Berger & Tom J. De Koning, 2011 Oct 7, In: Journal of Chromatography A. 1218, 40, p. 7130-7136 7 p.

    Research output: Contribution to journalArticle

  3. Intracranial bleeding due to vitamin K deficiency: Advantages of using a pediatric intensive care registry

    Désirée Y. Visser, Nicolaas J. Jansen, Marloes M. Ijland, Tom J. De Koning & Peter M. Van Hasselt, 2011 Jun 1, In: Intensive Care Medicine. 37, 6, p. 1014-1020 7 p.

    Research output: Contribution to journalArticle

  4. Essential polyunsaturated fatty acids in plasma and erythrocytes of children with inborn errors of amino acid metabolism

    H. Vlaardingerbroek, G. Hornstra, T. J. de Koning, J. A.M. Smeitink, H. D. Bakker, H. B.C. de Klerk & M. E. Rubio-Gozalbo, 2006 Jun 1, In: Molecular Genetics and Metabolism. 88, 2, p. 159-165 7 p.

    Research output: Contribution to journalArticle

  5. Expanding the ADCY5 phenotype toward spastic paraparesis: Amutation in the M2 domain

    Anne J.E. Waalkens, Fleur Vansenne, Annemarie H. Van Der Hout, Rodi Zutt, Jeroen Mourmans, Eduardo Tolosa, Tom J. De Koning & Marina A.J. Tijssen, 2018 Feb, In: Neurology: Genetics. 4, 1, e214.

    Research output: Contribution to journalArticle

  6. Ketogenic Diet in Refractory Childhood Epilepsy: Starting With a Liquid Formulation in an Outpatient Setting

    Amerins Weijenberg, Margreet van Rijn, Petra M C Callenbach, Tom J de Koning & Oebele F Brouwer, 2018 Jan, In: Child neurology open. 5

    Research output: Contribution to journalArticle

  7. De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability

    Iris G.M. Wijnen, Hermine E. Veenstra-Knol, Fleur Vansenne, Erica H. Gerkes, Tom de Koning, Yvonne J. Vos, Marina A.J. Tijssen, Deborah Sival, Niklas Darin, Els K. Vanhoutte, Mayke Oosterloo, Maartje Pennings, Bart P. van de Warrenburg & Erik Jan Kamsteeg, 2020 Mar 10, In: European Journal of Human Genetics.

    Research output: Contribution to journalArticle

  8. Association of 3-methylglutaconic aciduria with sensori-neural deafness, encephalopathy, and Leigh-like syndrome (MEGDEL association) in four patients with a disorder of the oxidative phosphorylation

    S. Wortmann, R. J.T. Rodenburg, M. Huizing, F. J. Loupatty, T. de Koning, L. A.J. Kluijtmans, U. Engelke, R. Wevers, J. A.M. Smeitink & E. Morava, 2006 May 1, In: Molecular Genetics and Metabolism. 88, 1, p. 47-52 6 p.

    Research output: Contribution to journalArticle

  9. Neurodegeneration with brain iron accumulation on MRI: An adult case of α-mannosidosis

    Evelien Zoons, Tom J. de Koning, Nico G.G.M. Abeling & Marina A.J. Tijssen, 2012 Jan 1, JIMD Reports. Springer Gabler, p. 99-102 4 p. (JIMD Reports; vol. 4).

    Research output: Chapter in Book/Report/Conference proceedingBook chapter

  10. A novel diagnostic approach to patients with myoclonus

    Rodi Zutt, Martje E. Van Egmond, Jan Willem Elting, Peter Jan Van Laar, Oebele F. Brouwer, Deborah A. Sival, Hubertus P. Kremer, Tom J. De Koning & Marina A. Tijssen, 2015 Dec 1, In: Nature Reviews Neurology. 11, p. 687-697

    Research output: Contribution to journalReview article

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