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Page 1
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.
Materna M, Delmonte OM, Bosticardo M, Momenilandi M, Conrey PE, Charmeteau-De Muylder B, Bravetti C, Bellworthy R, Cederholm A, Staels F, Ganoza CA, Darko S, Sayed S, Le Floc'h C, Ogishi M, Rinchai D, Guenoun A, Bolze A, Khan T, Gervais A, Krüger R, Völler M, Palterer B, Sadeghi-Shabestari M, Langlois de Septenville A, Schramm CA, Shah S, Tello-Cajiao JJ, Pala F, Amini K, Campos JS, Lima NS, Eriksson D, Lévy R, Seeleuthner Y, Jyonouchi S, Ata M, Al Ali F, Stittrich A, Deswarte C, Pereira A, Mégret J, Le Voyer T, Bastard P, Berteloot L, Dussiot M, Vladikine N, Cardenas PP, Jouanguy E, Alqahtani M, Hasan A, Thanaraj TA, Rosain J, Al Qureshah F, Sabato V, Alyanakian MA, Leruez-Ville M, Rozenberg F, Haddad E, Regueiro JR, Toribio ML, Kelsen JR, Salehi M, Nasiri S, Torabizadeh M, Rokni-Zadeh H, Changi-Ashtiani M, Vatandoost N, Moravej H, Akrami SM, Mazloomrezaei M, Cobat A, Meyts I, Toyofuku E, Nishimura M, Moriya K, Mizukami T, Imai K, Abel L, Malissen B, Al-Mulla F, Alkuraya FS, Parvaneh N, von Bernuth H, Beetz C, Davi F, Douek DC, Cheynier R, Langlais D, Landegren N, Marr N, Morio T, Shahrooei M, Schrijvers R, Henrickson SE, Luche H, Notarangelo LD, Casanova JL, Béziat V. Materna M, et al. Among authors: staels f. Science. 2024 Mar;383(6686):eadh4059. doi: 10.1126/science.adh4059. Epub 2024 Mar 1. Science. 2024. PMID: 38422122 Free PMC article.
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin.
Spaan AN, Neehus AL, Laplantine E, Staels F, Ogishi M, Seeleuthner Y, Rapaport F, Lacey KA, Van Nieuwenhove E, Chrabieh M, Hum D, Migaud M, Izmiryan A, Lorenzo L, Kochetkov T, Heesterbeek DAC, Bardoel BW, DuMont AL, Dobbs K, Chardonnet S, Heissel S, Baslan T, Zhang P, Yang R, Bogunovic D, Wunderink HF, Haas PA, Molina H, Van Buggenhout G, Lyonnet S, Notarangelo LD, Seppänen MRJ, Weil R, Seminario G, Gomez-Tello H, Wouters C, Mesdaghi M, Shahrooei M, Bossuyt X, Sag E, Topaloglu R, Ozen S, Leavis HL, van Eijk MMJ, Bezrodnik L, Blancas Galicia L, Hovnanian A, Nassif A, Bader-Meunier B, Neven B, Meyts I, Schrijvers R, Puel A, Bustamante J, Aksentijevich I, Kastner DL, Torres VJ, Humblet-Baron S, Liston A, Abel L, Boisson B, Casanova JL. Spaan AN, et al. Among authors: staels f. Science. 2022 Jun 17;376(6599):eabm6380. doi: 10.1126/science.abm6380. Epub 2022 Jun 17. Science. 2022. PMID: 35587511 Free PMC article.
DNA replication-associated inborn errors of immunity.
Willemsen M, Staels F, Gerbaux M, Neumann J, Schrijvers R, Meyts I, Humblet-Baron S, Liston A. Willemsen M, et al. Among authors: staels f. J Allergy Clin Immunol. 2023 Feb;151(2):345-360. doi: 10.1016/j.jaci.2022.11.003. Epub 2022 Nov 15. J Allergy Clin Immunol. 2023. PMID: 36395985 Free article. Review.
A double-edged sword.
Vandebotermet M, Staels F, Giovannozzi S, Delforge M, Tousseyn T, Steelandt T, Corveleyn A, Meyts I, Maertens J, Yserbyt J, Schrijvers R. Vandebotermet M, et al. Among authors: staels f. Breathe (Sheff). 2020 Sep;16(3):200017. doi: 10.1183/20734735.0017-2020. Breathe (Sheff). 2020. PMID: 33447267 Free PMC article.
Systemic autoinflammatory disease in adults.
Betrains A, Staels F, Schrijvers R, Meyts I, Humblet-Baron S, De Langhe E, Wouters C, Blockmans D, Vanderschueren S. Betrains A, et al. Among authors: staels f. Autoimmun Rev. 2021 Apr;20(4):102774. doi: 10.1016/j.autrev.2021.102774. Epub 2021 Feb 17. Autoimmun Rev. 2021. PMID: 33609798 Review.
Rituximab and improved nodular regenerative hyperplasia-associated non-cirrhotic liver disease in common variable immunodeficiency: a case report and literature study.
Roosens W, Staels F, Van Loo S, Humblet-Baron S, Meyts I, De Samblanx H, Verslype C, van Malenstein H, van der Merwe S, Laleman W, Schrijvers R. Roosens W, et al. Among authors: staels f. Front Immunol. 2023 Sep 19;14:1264482. doi: 10.3389/fimmu.2023.1264482. eCollection 2023. Front Immunol. 2023. PMID: 37795099 Free PMC article. Review.
Diagnosis of deficiency of adenosine deaminase type 2 in adulthood.
Betrains A, Staels F, Moens L, Delafontaine S, Hershfield MS, Blockmans D, Liston A, Humblet-Baron S, Meyts I, Schrijvers R, Vanderschueren S. Betrains A, et al. Among authors: staels f. Scand J Rheumatol. 2021 Nov;50(6):493-496. doi: 10.1080/03009742.2021.1881156. Epub 2021 Feb 25. Scand J Rheumatol. 2021. PMID: 33627040 No abstract available.
Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation.
Blommaert E, Cherepanova NA, Staels F, Wilson MP, Gilmore R, Schrijvers R, Jaeken J, Foulquier F, Matthijs G. Blommaert E, et al. Among authors: staels f. Hum Genet. 2022 Jul;141(7):1279-1286. doi: 10.1007/s00439-021-02400-1. Epub 2022 Feb 19. Hum Genet. 2022. PMID: 35182234
31 results