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Defective Sec61α1 underlies a novel cause of autosomal dominant severe congenital neutropenia.
Van Nieuwenhove E, Barber JS, Neumann J, Smeets E, Willemsen M, Pasciuto E, Prezzemolo T, Lagou V, Seldeslachts L, Malengier-Devlies B, Metzemaekers M, Haßdenteufel S, Kerstens A, van der Kant R, Rousseau F, Schymkowitz J, Di Marino D, Lang S, Zimmermann R, Schlenner S, Munck S, Proost P, Matthys P, Devalck C, Boeckx N, Claessens F, Wouters C, Humblet-Baron S, Meyts I, Liston A. Van Nieuwenhove E, et al. Among authors: devalck c. J Allergy Clin Immunol. 2020 Nov;146(5):1180-1193. doi: 10.1016/j.jaci.2020.03.034. Epub 2020 Apr 20. J Allergy Clin Immunol. 2020. PMID: 32325141 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: devalck c. 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.
[Autologous bone marrow graft in solid tumors in childhood].
Devalck C, Ferster A, De Laet MH, Nafa S, Bujan W, Azzi N, Ben Salah H, Corrazza F, Vergauwen P, Sariban E. Devalck C, et al. Rev Med Brux. 1992 Jun;13(6):201-6. Rev Med Brux. 1992. PMID: 1321485 Review. French.
[Bone marrow graft in hereditary diseases].
Bujan W, Ferster A, Devalck C, Vamos E, Mascart F, Denis R, Azzi N, Vergauwen P, Sariban E. Bujan W, et al. Among authors: devalck c. Rev Med Brux. 1992 Jun;13(6):207-11. Rev Med Brux. 1992. PMID: 1631420 French.
80 results