Management and Outcome in 32 Neonates with Thrombotic Events

por van Elteren, H. A., Veldt, H. S., te Pas, A. B., Roest, A. A. W., Smiers, F. J., Kollen, W. J., Sramek, A., Walther, F. J., Lopriore, E.
Publicado 2011

Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations

por Van Montfrans, J, Hartman, E, Braun, K, Hennekam, F, Hak, A, Nederkoorn, P, Westendorp, W, Bredius, R, Kollen, W, Scholvinck, E, Legger, G, Meyts, I, Liston, A, Lichtenbelt, K, Giltay, J, Van Haaften, G, De Vries Simons, G, Leavis, H, Nierkens, S, Sanders, C, Van Gijn, M
Publicado 2015