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Sarah J. Dyack

    Calculated based on number of publications stored in Pure and citations from PlumX
    Calculated based on number of publications stored in Pure and citations from PlumX
    Calculated based on number of publications stored in Pure and citations from PlumX
    19992023

    Research activity per year

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    • 2020

      Outcomes in pediatric studies of medium-chain acyl-coA dehydrogenase (MCAD) deficiency and phenylketonuria (PKU): A review

      Pugliese, M., Tingley, K., Chow, A., Pallone, N., Smith, M., Rahman, A., Chakraborty, P., Geraghty, M. T., Irwin, J., Tessier, L., Nicholls, S. G., Offringa, M., Butcher, N. J., Iverson, R., Clifford, T. J., Stockler, S., Hutton, B., Paik, K., Tao, J. & Skidmore, B. & 20 others, Coyle, D., Duddy, K., Dyack, S., Greenberg, C. R., Ghai, S. J., Karp, N., Korngut, L., Kronick, J., MacKenzie, A., MacKenzie, J., Maranda, B., Mitchell, J. J., Potter, M., Prasad, C., Schulze, A., Sparkes, R., Taljaard, M., Trakadis, Y., Walia, J. & Potter, B. K., Jan 14 2020, In: Orphanet Journal of Rare Diseases. 15, 1, 12.

      Research output: Contribution to journalReview articlepeer-review

      Open Access
      23 Citations (Scopus)
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