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Page 1
Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family.
Maalej M, Tej A, Bouguila J, Tilouche S, Majdoub S, Khabou B, Tabbebi M, Felhi R, Ammar M, Mkaouar-Rebai E, Keskes L, Boughamoura L, Fakhfakh F. Maalej M, et al. Among authors: tej a. Biochem Biophys Res Commun. 2018 Jan 8;495(2):1730-1737. doi: 10.1016/j.bbrc.2017.12.011. Epub 2017 Dec 5. Biochem Biophys Res Commun. 2018. PMID: 29217198
[Hepatopulmonary syndrome: a complication of type 1 Gaucher disease].
Bouguila J, Rouatbi H, Tej A, Chabchoub I, Trimech B, El Ajmi S, Essoussi AS, Boughammoura L. Bouguila J, et al. Among authors: tej a. Rev Pneumol Clin. 2012 Feb;68(1):58-62. doi: 10.1016/j.pneumo.2011.07.002. Epub 2011 Oct 13. Rev Pneumol Clin. 2012. PMID: 22305140 French.
Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy: detection of mutations in MT-ND2 and MT-TL1 genes.
Alila OF, Rebai EM, Tabebi M, Tej A, Chamkha I, Tlili A, Bouguila J, Tilouche S, Soyah N, Boughamoura L, Fakhfakh F. Alila OF, et al. Among authors: tej a. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Jul;27(4):2873-80. doi: 10.3109/19401736.2015.1060417. Epub 2015 Aug 10. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26258512
[Epstein-Barr virus infection and acute transverse myelitis].
Bouguila J, Tej A, Hasni I, Essoussi AS, Boughamoura L. Bouguila J, et al. Among authors: tej a. Med Mal Infect. 2012 Feb;42(2):83-4. doi: 10.1016/j.medmal.2011.05.014. Epub 2012 Jan 21. Med Mal Infect. 2012. PMID: 22266378 French. No abstract available.
11 results