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[Caudal regression syndrome].
Khemakhem R, Toumia HB, Francoise Ben Dridi M, Chaouachi B. Khemakhem R, et al. Among authors: francoise ben dridi m. Tunis Med. 2012 Apr;90(4):342. Tunis Med. 2012. PMID: 22535352 Free article. French. No abstract available.
Congenital hyperinsulinism: review of 12 Tunisian cases.
Ben Turkia H, Brahim K, Azzouz H, Tebib N, Abdelmoula MS, Ben Chehida A, Fekih M, Sayed S, Kaabar N, Francoise Ben Dridi M. Ben Turkia H, et al. Among authors: francoise ben dridi m. Tunis Med. 2011 Apr;89(4):369-73. Tunis Med. 2011. PMID: 21484688 Free article.
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.
Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F; Tunisian network on mental retardation study. Fendri-Kriaa N, et al. Biochem Biophys Res Commun. 2011 Jun 3;409(2):270-4. doi: 10.1016/j.bbrc.2011.04.140. Epub 2011 May 7. Biochem Biophys Res Commun. 2011. PMID: 21575601