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Page 1
[Neonatal hemoperitoneum].
Mekki M, Nouri A, Belghith M, Krichene I, Gargouri A, Sboui H, Sfar MT. Mekki M, et al. Among authors: sboui h. Arch Pediatr. 2000 Apr;7(4):385-7. doi: 10.1016/S0929-693X(00)88833-8. Arch Pediatr. 2000. PMID: 10793925 French.
[Neonatal hemorrhagic syndromes].
Salem N, Monastiri K, Bacha K, Guirat N, Sboui H, Jaidane S, Skouri H, Snoussi N. Salem N, et al. Among authors: sboui h. Arch Pediatr. 2001 Apr;8(4):374-80. doi: 10.1016/s0929-693x(00)00213-x. Arch Pediatr. 2001. PMID: 11339128 French.
Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: characterization of three novel polymorphisms.
Ben Charfeddine I, Riepe FG, Clauser E, Ayedi A, Makni S, Sfar MT, Sboui H, Kahloul N, Ben Hamouda H, Chouchane S, Trimech S, Zouari N, M'Rabet S, Amri F, Saad A, Holterhus PM, Gribaa M. Ben Charfeddine I, et al. Among authors: sboui h. Gene. 2012 Oct 1;507(1):20-6. doi: 10.1016/j.gene.2012.07.027. Epub 2012 Jul 25. Gene. 2012. PMID: 22841790
Transported neonates in Tunisia.
Chioukh FZ, Ben Ameur K, Monastiri K, Kbaier H, Blibech S, Douagi M, Ben Hlel K, Ben Hamouda H, Soua H, Bouraoui A, Régaieg R, Gargouri A, Ksibi I, Kacem S, Mahdhaoui N, Ayech H, Sboui H. Chioukh FZ, et al. Among authors: sboui h. Tunis Med. 2018 Dec;96(12):865-868. Tunis Med. 2018. PMID: 31131866 Free article.
[Hereditary sideroblastic anemia: a rare diagnosis].
Brahem-Jmili N, Salem N, Abdelkefi S, Champ BG, Bekri S, Sboui H, Mahjoub T, Yacoub S, Kortas M. Brahem-Jmili N, et al. Among authors: sboui h. Ann Biol Clin (Paris). 2004 May-Jun;62(3):349-52. Ann Biol Clin (Paris). 2004. PMID: 15217771 Free article. French.
18 results