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Homozygous DBF4 mutation as a cause of severe congenital neutropenia.
Willemsen M, Barber JS, Nieuwenhove EV, Staels F, Gerbaux M, Neumann J, Prezzemolo T, Pasciuto E, Lagou V, Boeckx N, Filtjens J, De Visscher A, Matthys P, Schrijvers R, Tousseyn T, O'Driscoll M, Bucciol G, Schlenner S, Meyts I, Humblet-Baron S, Liston A. Willemsen M, et al. Among authors: staels f. J Allergy Clin Immunol. 2023 Jul;152(1):266-277. doi: 10.1016/j.jaci.2023.02.016. Epub 2023 Feb 24. J Allergy Clin Immunol. 2023. PMID: 36841265 Free article.
Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype.
Blommaert E, Péanne R, Cherepanova NA, Rymen D, Staels F, Jaeken J, Race V, Keldermans L, Souche E, Corveleyn A, Sparkes R, Bhattacharya K, Devalck C, Schrijvers R, Foulquier F, Gilmore R, Matthijs G. Blommaert E, et al. Among authors: staels f. Proc Natl Acad Sci U S A. 2019 May 14;116(20):9865-9870. doi: 10.1073/pnas.1817815116. Epub 2019 Apr 29. Proc Natl Acad Sci U S A. 2019. PMID: 31036665 Free PMC article.
Inflammatory aortitis in a patient with type 2 hyper IgM syndrome.
Staels F, Betrains A, Willemsen M, Corvelyn A, Tousseyn T, Dierickx D, Humblet-Baron S, Liston A, Vanderschueren S, Schrijvers R. Staels F, et al. Rheumatology (Oxford). 2021 Mar 2;60(3):e87-e89. doi: 10.1093/rheumatology/keaa573. Rheumatology (Oxford). 2021. PMID: 32940674 No abstract available.
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.
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.
30 results