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X-linked Adrenoleukodystrophy, The Tunisian Experience.
Nasrallah F, Kraoua I, Zidi W, Omar S, Sanhaji H, Feki M, Ben Youssef IT, Kaabachi N. Nasrallah F, et al. Among authors: kraoua i. Clin Lab. 2015;61(10):1531-6. doi: 10.7754/clin.lab.2015.150318. Clin Lab. 2015. PMID: 26642716
Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian child.
Ben Younes T, Kraoua I, Benrhouma H, Nasrallah F, Ben Achour N, Klaa H, Hassen-Rouissi A, Drissi C, Benoist JF, Ben Youssef-Turki I. Ben Younes T, et al. Among authors: kraoua i. Arch Pediatr. 2017 Mar;24(3):241-243. doi: 10.1016/j.arcped.2016.11.019. Epub 2017 Jan 25. Arch Pediatr. 2017. PMID: 28131559
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment.
Mkaouar R, Riahi Z, Charfeddine C, Chelly I, Boudabbous H, Dallali H, Bonnet C, Hechmi M, Bekri S, Zitouna N, Zekri L, Tounsi A, Kefi R, Marrakchi J, Messaoud O, Kraoua I, Maalej S, Turki Ben Youssef I, Ben Hmid A, Giraudet F, Bouchoucha S, Tebib N, Besbes G, Petit C, Mrad R, Abdelhak S, Trabelsi M. Mkaouar R, et al. Among authors: kraoua i. PLoS One. 2021 Oct 6;16(10):e0258202. doi: 10.1371/journal.pone.0258202. eCollection 2021. PLoS One. 2021. PMID: 34614013 Free PMC article.
72 results