Resultats de la cerca - Staels, Frederik
- Mostrar 1 - 7 resultats de 7
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1
Monogenic Adult-Onset Inborn Errors of Immunity per Staels, Frederik, Collignon, Tom, Betrains, Albrecht, Gerbaux, Margaux, Willemsen, Mathijs, Humblet-Baron, Stephanie, Liston, Adrian, Vanderschueren, Steven, Schrijvers, Rik
Publicat 2021Text -
2
A double-edged sword per Vandebotermet, Martijn, Staels, Frederik, Giovannozzi, Simone, Delforge, Michel, Tousseyn, Thomas, Steelandt, Thomas, Corveleyn, Anniek, Meyts, Isabelle, Maertens, Johan, Yserbyt, Jonas, Schrijvers, Rik
Publicat 2020Text -
3
Primary Sjögren's syndrome and high type I interferon signalling in a kindred with C2 deficiency per Willemsen, Mathijs, Van Nieuwenhove, Erika, Seyed Tabib, Nasim Sadat, Staels, Frederik, Schrijvers, Rik, De Somer, Lien, Liston, Adrian, Humblet-Baron, Stephanie, Wouters, Carine
Publicat 2022Text -
4
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature per 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
Publicat 2020Text -
5
Case Report: VEXAS Syndrome: From Mild Symptoms to Life-Threatening Macrophage Activation Syndrome per 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
Publicat 2021Text -
6
Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype per 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
Publicat 2019Text -
7
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin per 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
Publicat 2022Text