Genetic variation in the functional ENG allele inherited from the non-affected parent associates with presence of pulmonary arteriovenous malformation in hereditary hemorrhagic tel... by Letteboer, Tom G W, Benzinou, Michael, Merrick, Christopher B, Quigley, David A, Zhau, Kechen, Kim, Il-Jin, To, Minh D, Jablons, David M, van Amstel, Johannes K P, Westermann, Cornelius J J, Giraud, Sophie, Dupuis-Girod, Sophie, Lesca, Gaetan, Berg, Jonathan H, Balmain, Allan, Akhurst, Rosemary J

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Haploinsufficiency of CUX1 Causes Nonsyndromic Global Developmental Delay With Possible Catch‐up Development by Platzer, Konrad, Cogné, Benjamin, Hague, Jennifer, Marcelis, Carlo L., Mitter, Diana, Oberndorff, Katrin, Park, Soo‐Mi, Ploos van Amstel, Hans K., Simonic, Ingrid, van der Smagt, Jasper J., Stegmann, Alexander P.A., Stevens, Servi J.C., Stumpel, Constance T.R.M., Vincent, Marie, Lemke, Johannes R., Jamra, Rami

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Heterogeneity of treatment effect of vilobelimab in COVID-19: a secondary analysis of a randomised controlled trial by van Amstel, Rombout B E, Slim, Marleen A, Lim, Endry H T, Rückinger, Simon, Seymour, Christopher W, Burnett, Bruce P, Bos, Lieuwe D J, van Vught, Lonneke A, Riedemann, Niels C, van de Beek, Diederik, Vlaar, Alexander P J

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Pharmacokinetic analysis of vilobelimab, anaphylatoxin C5a and antidrug antibodies in PANAMO: a phase 3 study in critically ill,  invasively mechanically ventilated COVID-19 patien... by Lim, Endry H. T., Vlaar, Alexander P. J., de Bruin, Sanne, Rückinger, Simon, Thielert, Claus, Habel, Maria, Guo, Renfeng, Burnett, Bruce P., Dickinson, James, Brouwer, Matthijs C., Riedemann, Niels C., van de Beek, Diederik

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