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  1. 2013

  2. Necrotizing enterocolitis and respiratory distress syndrome as first clinical presentation of mitochondrial trifunctional protein deficiency

    Diekman, E. F., Boelen, C. C. A., Prinsen, B. H. C. M. T., Ijlst, L., Duran, M., de Koning, T. J., Waterham, H. R., Wanders, R. J. A., Wijburg, F. A. & Visser, G., 2013, In: JIMD reports. 7, p. 1-6

    Research output: Contribution to journal › Article › Academic › peer-review

  3. Organic acid profile of isovaleric acidemia: a comprehensive metabolomics approach

    Dercksen, M., Koekemoer, G., Duran, M., Wanders, R. J. A., Mienie, L. J. & Reinecke, C. J., 2013, In: Metabolomics. 9, 4, p. 765-777

    Research output: Contribution to journal › Article › Academic › peer-review

  4. Polyunsaturated fatty acid concentration predicts myelin integrity in early-phase psychosis

    Peters, B. D., Machielsen, M. W. J., Hoen, W. P., Caan, M. W. A., Malhotra, A. K., Szeszko, P. R., Duran, M., Olabarriaga, S. D. & de Haan, L., 2013, In: Schizophrenia bulletin. 39, 4, p. 830-838

    Research output: Contribution to journal › Article › Academic › peer-review

  5. Red blood cell polyunsaturated fatty acids measured in red blood cells and schizophrenia: a meta-analysis

    Hoen, W. P., Lijmer, J. G., Duran, M., Wanders, R. J. A., van Beveren, N. J. M. & de Haan, L., 2013, In: Psychiatry research. 207, 1-2, p. 1-12

    Research output: Contribution to journal › Review article › Academic › peer-review

  6. S-adenosylmethionine and S-adenosylhomocysteine in plasma and cerebrospinal fluid in Rett syndrome and the effect of folinic acid supplementation

    Hagebeuk, E. E. O., Duran, M., Abeling, N. G. G. M., Vyth, A. & Poll-The, B. T., 2013, In: Journal of inherited metabolic disease. 36, 6, p. 967-972

    Research output: Contribution to journal › Article › Academic › peer-review

  7. Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism

    Violante, S., Ijlst, L., Ruiter, J., Koster, J., van Lenthe, H., Duran, M., de Almeida, I. T., Wanders, R. J. A., Houten, S. M. & Ventura, F. V., 2013, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. 1832, 6, p. 773-779

    Research output: Contribution to journal › Article › Academic › peer-review

  8. 2012

  9. Characterization of D-3-hydroxybutyrylcarnitine (ketocarnitine): an identified ketosis-induced metabolite

    Soeters, M. R., Serlie, M. J., Sauerwein, H. P., Duran, M., Ruiter, J. P., Kulik, W., Ackermans, M. T., Minkler, P. E., Hoppel, C. L., Wanders, R. J. A. & Houten, S. M., 2012, In: Metabolism: clinical and experimental. 61, 7, p. 966-973

    Research output: Contribution to journal › Article › Academic › peer-review

  10. Clinical variability of isovaleric acidemia in a genetically homogeneous population

    Dercksen, M., Duran, M., IJlst, L., Mienie, L. J., Reinecke, C. J., Ruiter, J. P. N., Waterham, H. R. & Wanders, R. J. A., 2012, In: Journal of inherited metabolic disease. 35, 6, p. 1021-1029

    Research output: Contribution to journal › Article › Academic › peer-review

  11. Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway

    Wanders, R. J. A., Duran, M. & Loupatty, F. J., 2012, In: Journal of inherited metabolic disease. 35, 1, p. 5-12

    Research output: Contribution to journal › Article › Academic › peer-review

  12. Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis

    Huijgen, R., Stork, A. D. M., Defesche, J. C., Peter, J., Alonso, R., Cuevas, A., Kastelein, J. J. P., Duran, M. & Stroes, E. S. G., 2012, In: Clinical genetics. 81, 1, p. 24-28

    Research output: Contribution to journal › Editorial › Academic › peer-review

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ID: 53781