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  1. 2021

  2. Exploring the metabolic fate of medium-chain triglycerides in healthy individuals using a stable isotope tracer

    Knottnerus, S. J. G., van Harskamp, D., Schierbeek, H., Bleeker, J. C., Crefcoeur, L. L., Ferdinandusse, S., van Goudoever, J. B., Houtkooper, R. H., IJlst, L., Langeveld, M., Wanders, R. J. A., Vaz, F. M., Wijburg, F. A. & Visser, G., Mar 2021, In: Clinical nutrition (Edinburgh, Scotland). 40, 3, p. 1396-1404 9 p.

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

  3. Management of conjunctival melanoma with local excision and adjuvant brachytherapy

    Brouwer, N. J., Marinkovic, M., Peters, F. P., Hulshof, M. C. C. M., Pieters, B. R., de Keizer, R. J. W., Horeweg, N., Laman, M. S., Bleeker, J. C., van Duinen, S. G., Jager, M. J., Creutzberg, C. L. & Luyten, G. P. M., Feb 2021, In: Eye (London, England). 35, 2, p. 490-498 9 p.

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

  4. Electrophysiological Abnormalities in VLCAD Deficient hiPSC-Cardiomyocytes Do not Improve with Carnitine Supplementation

    Verkerk, A. O., Knottnerus, S. J. G., Portero, V., Bleeker, J. C., Ferdinandusse, S., Guan, K., IJlst, L., Visser, G., Wanders, R. J. A., Wijburg, F. A., Bezzina, C. R., Mengarelli, I. & Houtkooper, R. H., 12 Jan 2021, In: Frontiers in pharmacology. 11, 616834.

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

  5. 2020

  6. Subclinical effects of long-chain fatty acid β-oxidation deficiency on the adult heart: A case-control magnetic resonance study

    Knottnerus, S. J. G., Bleeker, J. C., Ferdinandusse, S., Houtkooper, R. H., Langeveld, M., Nederveen, A. J., Strijkers, G. J., Visser, G., Wanders, R. J. A., Wijburg, F. A., Boekholdt, S. M. & Bakermans, A. J., 1 Sept 2020, In: Journal of inherited metabolic disease. 43, 5, p. 969-980 12 p.

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

  7. Nutritional ketosis improves exercise metabolism in patients with very long-chain acyl-CoA dehydrogenase deficiency

    Bleeker, J. C., Visser, G., Clarke, K., Ferdinandusse, S., de Haan, F. H., Houtkooper, R. H., IJlst, L., Kok, I. L., Langeveld, M., van der Pol, W. L., de Sain-van der Velden, M. G. M., Sibeijn-Kuiper, A., Takken, T., Wanders, R. J. A., van Weeghel, M., Wijburg, F. A., van der Woude, L. H., Wüst, R. C. I., Cox, P. J. & Jeneson, J. A. L., 1 Jul 2020, In: Journal of inherited metabolic disease. 43, 4, p. 787-799 13 p.

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

  8. Electrophysiological abnormalities in VLCAD deficient hiPSC-cardiomyocytes can be improved by lowering accumulation of fatty acid oxidation intermediates

    Knottnerus, S. J. G., Mengarelli, I., Wüst, R. C. I., Baartscheer, A., Bleeker, J. C., Coronel, R., Ferdinandusse, S., Guan, K., Ijlst, L., Li, W., Luo, X., Portero, V. M., Ulbricht, Y., Visser, G., Wanders, R. J. A., Wijburg, F. A., Verkerk, A. O., Houtkooper, R. H. & Bezzina, C. R., 1 Apr 2020, In: International journal of molecular sciences. 21, 7, 2589.

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

  9. 2019

  10. Impact of newborn screening for very-long-chain acyl-CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes

    Bleeker, J. C., Kok, I. L., Ferdinandusse, S., van der Pol, W. L., Cuppen, I., Bosch, A. M., Langeveld, M., Derks, T. G. J., Williams, M., de Vries, M., Mulder, M. F., Gozalbo, E. R., de Sain-van der Velden, M. G. M., Rennings, A. J., Schielen, P. J. C. I., Dekkers, E., Houtkooper, R. H., Waterham, H. R., Pras-Raves, M. L., Wanders, R. J. A., & 4 othersvan Hasselt, P. M., Schoenmakers, M., Wijburg, F. A. & Visser, G., May 2019, In: Journal of inherited metabolic disease. 42, 3, p. 414-423

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

  11. Proposal for an individualized dietary strategy in patients with very long-chain acyl-CoA dehydrogenase deficiency

    Bleeker, J. C., Kok, I. L., Ferdinandusse, S., de Vries, M., Derks, T. G. J., Mulder, M. F., Williams, M., Rubio Gozalbo, E., Bosch, A. M., van den Hurk, D. T., de Sain-van der Velden, M. G. M., Waterham, H. R., Wijburg, F. A. & Visser, G., Jan 2019, In: Journal of inherited metabolic disease. 42, 1, p. 159-168 10 p.

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

  12. Families with BAP1-tumor predisposition syndrome in The Netherlands: Path to identification and a proposal for genetic screening guidelines

    Chau, C., van Doorn, R., van Poppelen, N. M., van der Stoep, N., Mensenkamp, A. R., Sijmons, R. H., van Paassen, B. W., van den Ouweland, A. M. W., Naus, N. C., van der Hout, A. H., Potjer, T. P., Bleeker, F. E., Wevers, M. R., van Hest, L. P., Jongmans, M. C. J., Marinkovic, M., Bleeker, J. C., Jager, M. J., Luyten, G. P. M. & Nielsen, M., 2019, In: Cancers. 11, 8, 1114.

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

  13. 2018

  14. Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle

    Knottnerus, S. J. G., Bleeker, J. C., Wüst, R. C. I., Ferdinandusse, S., IJlst, L., Wijburg, F. A., Wanders, R. J. A., Visser, G. & Houtkooper, R. H., 2018, In: Reviews in endocrine & metabolic disorders. 19, 1, p. 93-106

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

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