Understanding acute metabolic decompensation in propionic and methylmalonic acidemias: a deep metabolic phenotyping approach

por Haijes, H. A., Jans, J. J. M., van der Ham, M., van Hasselt, P. M., Verhoeven-Duif, N. M.
Publicado 2020

ALG11-CDG: Three novel mutations and further characterization of the phenotype

por Regal, L., van Hasselt, P.M., Foulquier, F., Cuppen, I., Prinsen, HCMT, Jansen, K., Keldermans, L., De Meirleir, L., Matthijs, G., Jaeken, J.
Publicado 2014

B-cell depletion abrogates immune mediated cytopenia and rejection of cord blood transplantation in Hurler syndrome

por Nataraj, R., Hiwarkar, P., Bonney, D., Campbell, H., Jones, S., Deambrosis, D., Evans, P., Poulton, K., van Hasselt, P. M., Bierings, MB., Boelens, J. J., Lindemans, C. A., Wynn, R.
Publicado 2021

Development of a compounded propofol nanoemulsion using multiple non-invasive process analytical technologies

por Rooimans, T., Damen, M., Markesteijn, C.M.A., Schuurmans, C.C.L., de Zoete, N.H.C., van Hasselt, P.M., Hennink, W.E., van Nostrum, C.F., Hermes, M., Besseling, R., Vromans, H.
Publicado 2023

Rapid quantification of underivatized amino acids in plasma by hydrophilic interaction liquid chromatography (HILIC) coupled with tandem mass-spectrometry

por Prinsen, Hubertus C. M. T., Schiebergen-Bronkhorst, B. G. M., Roeleveld, M. W., Jans, J. J. M., de Sain-van der Velden, M. G. M., Visser, G., van Hasselt, P. M., Verhoeven-Duif, N. M.
Publicado 2016

Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions

por Renkema, G. H., Visser, G., Baertling, F., Wintjes, L. T., Wolters, V. M., van Montfrans, J., de Kort, G. A. P., Nikkels, P. G. J., van Hasselt, P. M., van der Crabben, S. N., Rodenburg, R. J. T.
Publicado 2017