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IRAK2 is associated with systemic lupus erythematosus risk.
Boumiza A, Zemni R, Sghiri R, Idriss N, Hassine HB, Chabchoub E, Mzabi A, Ghannouchi N, Bouajina E, Ben Hadj Slama F. Boumiza A, et al. Among authors: chabchoub e. Clin Rheumatol. 2020 Feb;39(2):419-424. doi: 10.1007/s10067-019-04781-1. Epub 2019 Oct 25. Clin Rheumatol. 2020. PMID: 31650390
IRAK2 is associated with susceptibility to rheumatoid arthritis.
Hassine HB, Sghiri R, Chabchoub E, Boumiza A, Slama F, Baccouche K, Shakoor Z, Almogren A, Mariaselvam C, Tamouza R, Bouajina E, Zemni R. Hassine HB, et al. Among authors: chabchoub e. Clin Rheumatol. 2018 Apr;37(4):927-933. doi: 10.1007/s10067-017-3906-0. Epub 2017 Nov 11. Clin Rheumatol. 2018. PMID: 29129009
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Jellouli NK, Hadj Salem I, Ellouz E, Kamoun Z, kamoun F, tlili A, Kaabachi N, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation study. Jellouli NK, et al. J Hum Genet. 2014 Apr;59(4):216-22. doi: 10.1038/jhg.2014.4. Epub 2014 Feb 27. J Hum Genet. 2014. PMID: 24573090
The role of enterovirus infections in type 1 diabetes in Tunisia.
Boussaid I, Boumiza A, Zemni R, Chabchoub E, Gueddah L, Slim I, Ben Hadj Slama F. Boussaid I, et al. Among authors: chabchoub e. J Pediatr Endocrinol Metab. 2017 Nov 27;30(12):1245-1250. doi: 10.1515/jpem-2017-0044. J Pediatr Endocrinol Metab. 2017. PMID: 29176023
Increased oxidative stress and altered levels of nitric oxide and peroxynitrite in Tunisian patients with chronic obstructive pulmonary disease: correlation with disease severity and airflow obstruction.
ben Anes A, Fetoui H, Bchir S, ben Nasr H, Chahdoura H, Chabchoub E, Yacoub S, Garrouch A, Benzarti M, Tabka Z, Chahed K. ben Anes A, et al. Among authors: chabchoub e. Biol Trace Elem Res. 2014 Oct;161(1):20-31. doi: 10.1007/s12011-014-0087-4. Epub 2014 Jul 31. Biol Trace Elem Res. 2014. PMID: 25074430
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome.
Rooryck C, Diaz-Font A, Osborn DP, Chabchoub E, Hernandez-Hernandez V, Shamseldin H, Kenny J, Waters A, Jenkins D, Kaissi AA, Leal GF, Dallapiccola B, Carnevale F, Bitner-Glindzicz M, Lees M, Hennekam R, Stanier P, Burns AJ, Peeters H, Alkuraya FS, Beales PL. Rooryck C, et al. Among authors: chabchoub e. Nat Genet. 2011 Mar;43(3):197-203. doi: 10.1038/ng.757. Epub 2011 Jan 23. Nat Genet. 2011. PMID: 21258343 Free PMC article.
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