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  1. 2017

  2. Germline deletion of Krüppel-like factor 14 does not increase risk of diet induced metabolic syndrome in male C57BL/6 mice

    Argmann, C. A., Violante, S., Dodatko, T., Amaro, M. P., Hagen, J., Gillespie, V. L., Buettner, C., Schadt, E. E. & Houten, S. M., 2017, In: BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS. 1863, 12, p. 3277-3285

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

  3. 2016

  4. The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders

    Houten, S. M., Violante, S., Ventura, F. V. & Wanders, R. J. A., 2016, In: Annual review of physiology. 78, p. 23-44

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

  5. 2013

  6. Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines

    Violante, S., Ijlst, L., te Brinke, H., Tavares de Almeida, I., Wanders, R. J. A., Ventura, F. V. & Houten, S. M., 2013, In: FASEB journal. 27, 5, p. 2039-2044

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

  7. Novel aspects of carnitine function and metabolism

    Violante, S., 2013

    Research output: Thesis › Phd-Thesis - Research and graduation external

  8. Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient

    Violante, S., Ijlst, L., te Brinke, H., Koster, J., Tavares de Almeida, I., Wanders, R. J. A., Ventura, F. V. & Houten, S. M., 2013, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS. 1831, 9, p. 1467-1474

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

  9. 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

  10. 2012

  11. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism

    Celestino-Soper, P. B. S., Violante, S., Crawford, E. L., Luo, R., Lionel, A. C., Delaby, E., Cai, G., Sadikovic, B., Lee, K., Lo, C., Gao, K., Person, R. E., Moss, T. J., German, J. R., Huang, N., Shinawi, M., Treadwell-Deering, D., Szatmari, P., Roberts, W., Fernandez, B., & 16 othersSchroer, R. J., Stevenson, R. E., Buxbaum, J. D., Betancur, C., Scherer, S. W., Sanders, S. J., Geschwind, D. H., Sutcliffe, J. S., Hurles, M. E., Wanders, R. J. A., Shaw, C. A., Leal, S. M., Cook, E. H., Goin-Kochel, R. P., Vaz, F. M. & Beaudet, A. L., 2012, In: Proceedings of the National Academy of Sciences of the United States of America. 109, 21, p. 7974-7981

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

  12. 2010

  13. Carnitine palmitoyltransferase 2: New insights on the substrate specificity and implications for acylcarnitine profiling

    Violante, S., Ijlst, L., van Lenthe, H., de Almeida, I. T., Wanders, R. J. & Ventura, F. V., 2010, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE. 1802, 9, p. 728-732

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

ID: 76106