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Page 1
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. Among authors: ellouz e. 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
[Neurological complications of neurofibromatosis type 1. Moya Moya syndrome].
Hsairi-Guidara I, Fourati H, Kamoun F, Ellouz E, Ayadi I, Ben Othmen H, Mnif Z, Triki C. Hsairi-Guidara I, et al. Among authors: ellouz e. Arch Pediatr. 2015 Jan;22(1):90-1, 106-8. doi: 10.1016/j.arcped.2014.10.013. Epub 2014 Nov 4. Arch Pediatr. 2015. PMID: 25466783 French. No abstract available.
[Study of a Tunisian population of children with learning disorders].
Hsairi Guidara I, Ayadi I, Ellouz E, Abid I, Kamoun F, Hakim L, Kassis F, Kolsi D, Moalla F, Ghribi F, Triki CC. Hsairi Guidara I, et al. Among authors: ellouz e. Tunis Med. 2013 Jun;91(6):382-6. Tunis Med. 2013. PMID: 23868035 Free article. French.