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Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds.
Prando C, Samarina A, Bustamante J, Boisson-Dupuis S, Cobat A, Picard C, AlSum Z, Al-Jumaah S, Al-Hajjar S, Frayha H, Al-Mousa H, Ben-Mustapha I, Adimi P, Feinberg J, de Suremain M, Jannière L, Filipe-Santos O, Mansouri N, Stephan JL, Nallusamy R, Kumararatne DS, Bloorsaz MR, Ben-Ali M, Elloumi-Zghal H, Chemli J, Bouguila J, Bejaoui M, Alaki E, AlFawaz TS, Al Idrissi E, ElGhazali G, Pollard AJ, Murugasu B, Wah Lee B, Halwani R, Al-Zahrani M, Al Shehri MA, Al-Zahrani M, Bin-Hussain I, Mahdaviani SA, Parvaneh N, Abel L, Mansouri D, Barbouche R, Al-Muhsen S, Casanova JL. Prando C, et al. Among authors: elloumi zghal h. Medicine (Baltimore). 2013 Mar;92(2):109-122. doi: 10.1097/MD.0b013e31828a01f9. Medicine (Baltimore). 2013. PMID: 23429356 Free PMC article.
A 1,100-year-old founder effect mutation in IL12B gene is responsible for Mendelian susceptibility to mycobacterial disease in Tunisian patients.
Ben-Mustapha I, Ben-Ali M, Mekki N, Patin E, Harmant C, Bouguila J, Elloumi-Zghal H, Harbi A, Béjaoui M, Boughammoura L, Chemli J, Barbouche MR. Ben-Mustapha I, et al. Among authors: elloumi zghal h. Immunogenetics. 2014 Jan;66(1):67-71. doi: 10.1007/s00251-013-0739-0. Epub 2013 Oct 15. Immunogenetics. 2014. PMID: 24127073
Activation induced cytidine deaminase mutant (AID-His130Pro) from Hyper IgM 2 patient retained mutagenic activity on SHM artificial substrate.
Ouadani H, Ben-Mustapha I, Ben-Ali M, Larguèche B, Jovanic T, Garcia S, Arcangioli B, Elloumi-Zghal H, Fathallah D, Hachicha M, Masmoudi H, Rougeon F, Barbouche MR. Ouadani H, et al. Among authors: elloumi zghal h. Mol Immunol. 2016 Nov;79:77-82. doi: 10.1016/j.molimm.2016.09.025. Epub 2016 Oct 4. Mol Immunol. 2016. PMID: 27716525 Free article.
Genetics and genomic medicine in Tunisia.
Elloumi-Zghal H, Chaabouni Bouhamed H. Elloumi-Zghal H, et al. Mol Genet Genomic Med. 2018 Mar;6(2):134-159. doi: 10.1002/mgg3.392. Mol Genet Genomic Med. 2018. PMID: 29663716 Free PMC article.
[Homozygous antithrombin type HBS deficiency; a family study].
Guermazi S, Elloumi-ZghaL H, Ben Hassine L, Romani S, Khalfallah N, Abdelhak S, Dellagi K. Guermazi S, et al. Among authors: elloumi zghal h. Pathol Biol (Paris). 2007 Jun;55(5):256-61. doi: 10.1016/j.patbio.2006.10.006. Epub 2006 Nov 29. Pathol Biol (Paris). 2007. PMID: 17140748 French.
Lack of association between the angiotensin-converting enzyme gene (I/D) polymorphism and diabetic nephropathy in Tunisian type 2 diabetic patients.
Arfa I, Abid A, Nouira S, Elloumi-Zghal H, Malouche D, Mannai I, Zorgati MM, Ben Alaya N, Rebai A, Zouari B, Ben Ammar S, Ben Rayana MC, Hmida S, Blousa-Chabchoub S, Abdelhak S. Arfa I, et al. Among authors: elloumi zghal h. J Renin Angiotensin Aldosterone Syst. 2008 Mar;9(1):32-6. doi: 10.3317/jraas.2008.002. J Renin Angiotensin Aldosterone Syst. 2008. PMID: 18404607 Free article.