Meyts I - Search Results

1

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia.

Zhang Q, Matuozzo D, Le Pen J, Lee D, Moens L, Asano T, Bohlen J, Liu Z, Moncada-Velez M, Kendir-Demirkol Y, Jing H, Bizien L, Marchal A, Abolhassani H, Delafontaine S, Bucciol G; COVID Human Genetic Effort; Bayhan GI, Keles S, Kiykim A, Hancerli S, Haerynck F, Florkin B, Hatipoglu N, Ozcelik T, Morelle G, Zatz M, Ng LFP, Lye DC, Young BE, Leo YS, Dalgard CL, Lifton RP, Renia L, Meyts I, Jouanguy E, Hammarström L, Pan-Hammarström Q, Boisson B, Bastard P, Su HC, Boisson-Dupuis S, Abel L, Rice CM, Zhang SY, Cobat A, Casanova JL. Zhang Q, et al. Among authors: meyts i. J Exp Med. 2022 Aug 1;219(8):e20220131. doi: 10.1084/jem.20220131. Epub 2022 Jun 16. J Exp Med. 2022. PMID: 35708626 Free PMC article.

2

Human memory B lymphocyte subsets fulfill distinct roles in the anti-polysaccharide and anti-protein immune response.

Moens L, Wuyts M, Meyts I, De Boeck K, Bossuyt X. Moens L, et al. Among authors: meyts i. J Immunol. 2008 Oct 15;181(8):5306-12. doi: 10.4049/jimmunol.181.8.5306. J Immunol. 2008. PMID: 18832686

3

Laboratory diagnosis of specific antibody deficiency to pneumococcal capsular polysaccharide antigens by multiplexed bead assay.

Borgers H, Moens L, Picard C, Jeurissen A, Raes M, Sauer K, Proesmans M, De Boeck K, Casanova JL, Meyts I, Bossuyt X. Borgers H, et al. Among authors: meyts i. Clin Immunol. 2010 Feb;134(2):198-205. doi: 10.1016/j.clim.2009.10.006. Epub 2009 Nov 13. Clin Immunol. 2010. PMID: 19914139

4

Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report.

De Somer L, Wouters C, Morren MA, De Vos R, Van Den Oord J, Devriendt K, Meyts I. De Somer L, et al. Among authors: meyts i. Orphanet J Rare Dis. 2010 Dec 8;5:37. doi: 10.1186/1750-1172-5-37. Orphanet J Rare Dis. 2010. PMID: 21143835 Free PMC article.

5

Coprescription of antibiotics and asthma drugs in children.

De Boeck K, Vermeulen F, Meyts I, Hutsebaut L, Franckaert D, Proesmans M. De Boeck K, et al. Among authors: meyts i. Pediatrics. 2011 Jun;127(6):1022-6. doi: 10.1542/peds.2009-3068. Epub 2011 May 23. Pediatrics. 2011. PMID: 21606144

6

Addressing diagnostic challenges in primary immunodeficiencies: laboratory evaluation of Toll-like receptor- and NF-κB-mediated immune responses.

Frans G, Meyts I, Picard C, Puel A, Zhang SY, Moens L, Wuyts G, Van der Werff Ten Bosch J, Casanova JL, Bossuyt X. Frans G, et al. Among authors: meyts i. Crit Rev Clin Lab Sci. 2014 Apr;51(2):112-23. doi: 10.3109/10408363.2014.881317. Epub 2014 Feb 18. Crit Rev Clin Lab Sci. 2014. PMID: 24533908 Review.

7

Diagnostic accuracy of nitric oxide measurements to detect primary ciliary dyskinesia.

Boon M, Meyts I, Proesmans M, Vermeulen FL, Jorissen M, De Boeck K. Boon M, et al. Among authors: meyts i. Eur J Clin Invest. 2014 May;44(5):477-85. doi: 10.1111/eci.12254. Eur J Clin Invest. 2014. PMID: 24597492

8

Value of allohaemagglutinins in the diagnosis of a polysaccharide antibody deficiency.

Schaballie H, Vermeulen F, Verbinnen B, Frans G, Vermeulen E, Proesmans M, De Vreese K, Emonds MP, De Boeck K, Moens L, Picard C, Bossuyt X, Meyts I. Schaballie H, et al. Among authors: meyts i. Clin Exp Immunol. 2015 May;180(2):271-9. doi: 10.1111/cei.12571. Clin Exp Immunol. 2015. PMID: 25516411 Free PMC article. Clinical Trial.

9

PID in Disguise: Molecular Diagnosis of IRAK-4 Deficiency in an Adult Previously Misdiagnosed With Autosomal Dominant Hyper IgE Syndrome.

Frans G, Moens L, Schrijvers R, Wuyts G, Bouckaert B, Schaballie H, Dupont L, Bossuyt X, Corveleyn A, Meyts I. Frans G, et al. Among authors: meyts i. J Clin Immunol. 2015 Nov;35(8):739-44. doi: 10.1007/s10875-015-0205-x. Epub 2015 Oct 15. J Clin Immunol. 2015. PMID: 26472314

10

Mild humoral immunodeficiency in a patient with X-linked Kabuki syndrome.

Frans G, Meyts I, Devriendt K, Liston A, Vermeulen F, Bossuyt X. Frans G, et al. Among authors: meyts i. Am J Med Genet A. 2016 Mar;170(3):801-3. doi: 10.1002/ajmg.a.37499. Epub 2015 Dec 24. Am J Med Genet A. 2016. PMID: 26701671 No abstract available.

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