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A putative disease-associated haplotype within the SCN1A gene in Dravet syndrome.
Fendri-Kriaa N, Boujilbene S, Kammoun F, Mkaouar-Rebai E, Ben Mahmoud A, Hsairi I, Rebai A, Triki C, Fakhfakh F. Fendri-Kriaa N, et al. Among authors: hsairi i. Biochem Biophys Res Commun. 2011 May 20;408(4):654-7. doi: 10.1016/j.bbrc.2011.04.079. Epub 2011 Apr 21. Biochem Biophys Res Commun. 2011. PMID: 21531204
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. Among authors: hsairi i. 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
A Novel Mutation p.A59P in N-Terminal Domain of Methyl-CpG-Binding Protein 2 Confers Phenotypic Variability in 3 Cases of Tunisian Rett Patients: Clinical Evaluations and In Silico Investigations.
Kharrat M, Hsairi I, Fendri-Kriaa N, Kenoun H, Othmen HB, Ben Mahmoud A, Ghorbel R, Abid I, Triki C, Fakhfakh F. Kharrat M, et al. Among authors: hsairi i. J Child Neurol. 2015 Nov;30(13):1715-21. doi: 10.1177/0883073815578529. Epub 2015 Apr 10. J Child Neurol. 2015. PMID: 25862735
MRI features in 17 patients with l2 hydroxyglutaric aciduria.
Fourati H, Ellouze E, Ahmadi M, Chaari D, Kamoun F, Hsairi I, Triki C, Mnif Z. Fourati H, et al. Among authors: hsairi i. Eur J Radiol Open. 2016 Sep 27;3:245-250. doi: 10.1016/j.ejro.2016.09.001. eCollection 2016. Eur J Radiol Open. 2016. PMID: 27709120 Free PMC article.
13 results