Canlyniadau Chwilio - Staels, Frederik
- Dangos 1 - 7 canlyniadau o 7
-
1
Monogenic Adult-Onset Inborn Errors of Immunity gan Staels, Frederik, Collignon, Tom, Betrains, Albrecht, Gerbaux, Margaux, Willemsen, Mathijs, Humblet-Baron, Stephanie, Liston, Adrian, Vanderschueren, Steven, Schrijvers, Rik
Cyhoeddwyd 2021Text -
2
A double-edged sword gan Vandebotermet, Martijn, Staels, Frederik, Giovannozzi, Simone, Delforge, Michel, Tousseyn, Thomas, Steelandt, Thomas, Corveleyn, Anniek, Meyts, Isabelle, Maertens, Johan, Yserbyt, Jonas, Schrijvers, Rik
Cyhoeddwyd 2020Text -
3
Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency gan Willemsen, Mathijs, Van Nieuwenhove, Erika, Seyed Tabib, Nasim Sadat, Staels, Frederik, Schrijvers, Rik, De Somer, Lien, Liston, Adrian, Humblet-Baron, Stephanie, Wouters, Carine
Cyhoeddwyd 2022Text -
4
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature gan Staels, Frederik, Betrains, Albrecht, Doubel, Peter, Willemsen, Mathijs, Cleemput, Vincent, Vanderschueren, Steven, Corveleyn, Anniek, Meyts, Isabelle, Sprangers, Ben, Crow, Yanick J., Humblet-Baron, Stephanie, Liston, Adrian, Schrijvers, Rik
Cyhoeddwyd 2020Text -
5
Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome gan Staels, Frederik, Betrains, Albrecht, Woei-A-Jin, F. J. Sherida H., Boeckx, Nancy, Beckers, Marielle, Bervoets, An, Willemsen, Mathijs, Neerinckx, Barbara, Humblet-Baron, Stephanie, Blockmans, Daniel Engelbert, Vanderschueren, Steven, Schrijvers, Rik
Cyhoeddwyd 2021Text -
6
Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype gan Blommaert, Eline, Péanne, Romain, Cherepanova, Natalia A., Rymen, Daisy, Staels, Frederik, Jaeken, Jaak, Race, Valérie, Keldermans, Liesbeth, Souche, Erika, Corveleyn, Anniek, Sparkes, Rebecca, Bhattacharya, Kaustuv, Devalck, Christine, Schrijvers, Rik, Foulquier, François, Gilmore, Reid, Matthijs, Gert
Cyhoeddwyd 2019Text -
7
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin gan Spaan, András N., Neehus, Anna-Lena, Laplantine, Emmanuel, Staels, Frederik, Ogishi, Masato, Seeleuther, Yoann, Rapaport, Franck, Lacey, Keenan A., Van Nieuwenhove, Erika, Chrabieh, Maya, Hum, David, Migaud, Mélanie, Izmiryan, Araksya, Lorenzo, Lazaro, Kochetkov, Tatiana, Heesterbeek, Dani A.C., Bardoel, Bart W., DuMont, Ashley L., Dobbs, Kerry, Chardonnet, Solenne, Heissel, Søren, Baslan, Timour, Zhang, Peng, Yang, Rui, Bogunovic, Dusan, Wunderink, Herman F., Haas, Pieter-Jan A., Molina, Henrik, Van Buggenhout, Griet, Lyonnet, Stanislas, Notarangelo, Luigi D., Seppänen, Mikko R.J., Weil, Robert, Seminario, Gisela, Gomez-Tello, Héctor, Wouters, Carine, Mesdaghi, Mehrnaz, Shahrooei, Mohammad, Bossuyt, Xavier, Sag, Erdal, Topaloglu, Rezan, Ozen, Seza, Leavis, Helen L., van Eijk, Maarten M.J., Bezrodnik, Liliana, Galicia, Lizbeth Blancas, Hovnanian, Alain, Nassif, Aude, Bader-Meunier, Brigitte, Neven, Bénédicte, Meyts, Isabelle, Schrijvers, Rik, Puel, Anne, Bustamante, Jacinta, Aksentijevich, Ivona, Kastner, Daniel, Torres, Victor J., Humblet-Baron, Stéphanie, Liston, Adrian, Abel, Laurent, Boisson, Bertrand, Casanova, Jean-Laurent
Cyhoeddwyd 2022Text