Minela Haskovic

Research output

Research output per year 2019 2020 2022

• 3 Article
• 1 (Systematic) Review article
• 1 Doctoral Thesis

Research output per year

Research output per year

Search results

• 2022

  Novel mRNA therapy restores GALT protein and enzyme activity in a zebrafish model of classic galactosemia

  Delnoy, B., Haskovic, M., Vanoevelen, J., Steinbusch, L. K. M., Vos, E. N., Knoops, K., Zimmermann, L. J. I., Noga, M., Lefeber, D. J., Martini, P. G. V., Coelho, A. I. & Rubio-Gozalbo, M. E., Jul 2022, In: Journal of Inherited Metabolic Disease. 45, 4, p. 748-758 11 p.

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

  Open Access
• 2020

  Classic galactosemia: natural history and new treatment approaches

  Haskovic, M., 2020, Maastricht: ProefschriftMaken.

  Research output: Thesis › Doctoral Thesis › Internal

  Open Access

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  1102 Downloads (Pure)

• Nucleotide sugar profiles throughout development in wildtype andgaltknockout zebrafish

  Haskovic, M., Coelho, A. I., Lindhout, M., Zijlstra, F., Veizaj, R., Vos, R., Vanoevelen, J. M., Bierau, J., Lefeber, D. J. & Rubio-Gozalbo, M. E., Sept 2020, In: Journal of Inherited Metabolic Disease. 43, 5, p. 994-1001 8 p.

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

  Open Access

• Pathophysiology and targets for treatment in hereditary galactosemia: A systematic review of animal and cellular models

  Haskovic, M., Coelho, A. I., Bierau, J., Vanoevelen, J. M., Steinbusch, L. K. M., Zimmermann, L. J. I., Villamor-Martinez, E., Berry, G. T. & Rubio-Gozalbo, M. E., May 2020, In: Journal of Inherited Metabolic Disease. 43, 3, p. 392-408 17 p.

  Research output: Contribution to journal › (Systematic) Review article › peer-review

  Open Access
• 2019

  The natural history of classic galactosemia: lessons from the GalNet registry

  Rubio-Gozalbo, M. E., Haskovic, M., Bosch, A. M., Burnyte, B., Coelho, A. I., Cassiman, D., Couce, M. L., Dawson, C., Demirbas, D., Derks, T., Eyskens, F., Forga, M. T., Grunewald, S., Haberle, J., Hochuli, M., Hubert, A., Huidekoper, H. H., Janeiro, P., Kotzka, J., Knerr, I., & 23 othersLabrune, P., Landau, Y. E., Langendonk, J. G., Moeslinger, D., Mueller-Wieland, D., Murphy, E., Ounap, K., Ramadza, D., Rivera, I. A., Scholl-Buergi, S., Stepien, K. M., Thijs, A., Tran, C., Vara, R., Visser, G., Vos, R., de Vries, M., Waisbren, S. E., Welsink-Karssies, M. M., Wortmann, S. B., Gautschi, M., Treacy, E. P. & Berry, G. T., 27 Apr 2019, In: Orphanet Journal of Rare Diseases. 14, 11 p., 86.

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

  Open Access