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The challenges of classical galactosemia: HRQoL in pediatric and adult patients
Hermans, M. E., van Oers, H. A., Geurtsen, G. J., Haverman, L., Hollak, C. E. M., Rubio-Gozalbo, M. E. & Bosch, A. M., Dec 2023, In: Orphanet Journal of Rare Diseases. 18, 1, p. 135 135.Research output: Contribution to journal › Article › Academic › peer-review
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Multi-omics in classical galactosemia: Evidence for the involvement of multiple metabolic pathways
Hermans, M. E., van Weeghel, M., Vaz, F. M., Ferdinandusse, S., Hollak, C. E. M., Huidekoper, H. H., Janssen, M. C. H., van Kuilenburg, A. B. P., Pras-Raves, M. L., Wamelink, M. M. C., Wanders, R. J. A., Welsink-Karssies, M. M. & Bosch, A. M., Nov 2022, In: Journal of Inherited Metabolic Disease. 45, 6, p. 1094-1105 12 p.Research output: Contribution to journal › Article › Academic › peer-review
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