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Page 1
Terminal Complement Pathway Deficiency in an Adult Patient with Meningococcal Sepsis.
Staels F, Meersseman W, Stordeur P, Willekens K, Van Loo S, Corveleyn A, Meyts I, Meyfroidt G, Schrijvers R. Staels F, et al. Among authors: corveleyn a. Case Reports Immunol. 2022 May 23;2022:9057000. doi: 10.1155/2022/9057000. eCollection 2022. Case Reports Immunol. 2022. PMID: 35655932 Free PMC article.
Successful hematopoietic stem cell transplantation for myelofibrosis in an adult with warts-hypogammaglobulinemia-immunodeficiency-myelokathexis syndrome.
Moens L, Frans G, Bosch B, Bossuyt X, Verbinnen B, Poppe W, Boeckx N, Slatter M, Brusselmans C, Diaz G, Tousseyn T, Flipts H, Corveleyn A, Dierickx D, Meyts I. Moens L, et al. Among authors: corveleyn a. J Allergy Clin Immunol. 2016 Nov;138(5):1485-1489.e2. doi: 10.1016/j.jaci.2016.04.057. Epub 2016 Jul 12. J Allergy Clin Immunol. 2016. PMID: 27484033 No abstract available.
Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling.
Melki I, Rose Y, Uggenti C, Van Eyck L, Frémond ML, Kitabayashi N, Rice GI, Jenkinson EM, Boulai A, Jeremiah N, Gattorno M, Volpi S, Sacco O, Terheggen-Lagro SWJ, Tiddens HAWM, Meyts I, Morren MA, De Haes P, Wouters C, Legius E, Corveleyn A, Rieux-Laucat F, Bodemer C, Callebaut I, Rodero MP, Crow YJ. Melki I, et al. Among authors: corveleyn a. J Allergy Clin Immunol. 2017 Aug;140(2):543-552.e5. doi: 10.1016/j.jaci.2016.10.031. Epub 2017 Jan 10. J Allergy Clin Immunol. 2017. PMID: 28087229
Human DOCK2 Deficiency: Report of a Novel Mutation and Evidence for Neutrophil Dysfunction.
Moens L, Gouwy M, Bosch B, Pastukhov O, Nieto-Patlàn A, Siler U, Bucciol G, Mekahli D, Vermeulen F, Desmet L, Maebe S, Flipts H, Corveleyn A, Moshous D, Philippet P, Tangye SG, Boisson B, Casanova JL, Florkin B, Struyf S, Reichenbach J, Bustamante J, Notarangelo LD, Meyts I. Moens L, et al. Among authors: corveleyn a. J Clin Immunol. 2019 Apr;39(3):298-308. doi: 10.1007/s10875-019-00603-w. Epub 2019 Mar 5. J Clin Immunol. 2019. PMID: 30838481 Free PMC 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: corveleyn a. 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.
Hyperhomocysteinemia: a trigger for complement-mediated TMA?
Bernards J, Doubel P, Meeus G, Lerut E, Corveleyn A, Van Den Heuvel LP, Meersseman W, Kuypers DK, Claes KJ. Bernards J, et al. Among authors: corveleyn a. Acta Clin Belg. 2021 Feb;76(1):65-69. doi: 10.1080/17843286.2019.1649039. Epub 2019 Aug 11. Acta Clin Belg. 2021. PMID: 31401947
Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature.
Staels F, Betrains A, Doubel P, Willemsen M, Cleemput V, Vanderschueren S, Corveleyn A, Meyts I, Sprangers B, Crow YJ, Humblet-Baron S, Liston A, Schrijvers R. Staels F, et al. Among authors: corveleyn a. Front Immunol. 2020 Sep 29;11:575219. doi: 10.3389/fimmu.2020.575219. eCollection 2020. Front Immunol. 2020. PMID: 33133092 Free PMC 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: corveleyn a. Breathe (Sheff). 2020 Sep;16(3):200017. doi: 10.1183/20734735.0017-2020. Breathe (Sheff). 2020. PMID: 33447267 Free PMC article.
65 results