Paula Alexandra Videira

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2019
Corrigendum to: International clinical guidelines for the management of phosphomannomutase 2-congenital disorders of glycosylation: Diagnosis, treatment and follow up (Journal of Inherited Metabolic Disease, (2019), 42, 1, (5-28), 10.1002/jimd.12024)
Altassan, R., Péanne, R., Jaeken, J., Barone, R., Bidet, M., Borgel, D., Brasil, S., Cassiman, D., Cechova, A., Coman, D., Corral, J., Correia, J., Morena-Barrio, M. E. D. L., Lonlay, P. D., Ferreira, V. D. R., Ferreira, C. R., Fiumara, A., Francisco, R., Freeze, H., Funke, S., & 34 othersGardeitchik, T., Gert, M., Girad, M., Giros, M., Grünewald, S., Hernández-Caselles, T., Honzik, T., Hutter, M., Krasnewich, D., Lam, C., Lee, J., Lefeber, D., Marques-Da-Silva, D., Martinez, A. F., Moravej, H., Ounap, K., Pascoal, C., Pascreau, T., Patterson, M., Quelhas, D., Raymond, K., Sarkhail, P., Schiff, M., Seroczyńska, M., Serrano, M., Seta, N., Sykut-Cegielska, J., Thiel, C., Tort, F., Vals, M-A., Videira, P. A., Witters, P., Zeevaert, R. & Morava, E., 1 May 2019, In: Journal of Inherited Metabolic Disease. 42, 3, 1 p.
Research output: Contribution to journal › Comment/debate › peer-review
2 Citations (Scopus)

Research output