Ben Rebeh I - Search Results

1

Prevalence of comorbid asthma in Tunisian patients with COVID-19: clinical features and outcomes.

Ben Rebeh I, Gargouri M, Ghariani M, Kallel N, Rouis S, Marrakchi W, Chebil D, Ben Marzoug R, Gargouri H, Merzougui L, Ghorbel H, Chakroun M, Hadj Kacem H, Rebai A. Ben Rebeh I, et al. J Infect Dev Ctries. 2023 Dec 31;17(12):1706-1713. doi: 10.3855/jidc.17485. J Infect Dev Ctries. 2023. PMID: 38252725 Free article.

2

Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis.

Ben-Rebeh I, Grati M, Bonnet C, Bouassida W, Hadjamor I, Ayadi H, Ghorbel A, Petit C, Masmoudi S. Ben-Rebeh I, et al. Mol Vis. 2016 Jul 19;22:827-35. eCollection 2016. Mol Vis. 2016. PMID: 27440999 Free PMC article.

3

Molecular Analysis of Libyan Families with Allgrove Syndrome: Geographic Expansion of the Ancestral Mutation c.1331+1G>A in North Africa.

Kallabi F, Ben Rebeh I, Felhi R, Sellami D, Masmoudi S, Keskes L, Kamoun H. Kallabi F, et al. Among authors: ben rebeh i. Horm Res Paediatr. 2016;85(1):18-21. doi: 10.1159/000441653. Epub 2015 Nov 24. Horm Res Paediatr. 2016. PMID: 26595337

4

Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene.

Hertecant JL, Ben-Rebeh I, Marah MA, Abbas T, Ayadi L, Ben Salem S, Al-Jasmi FA, Al-Gazali L, Al-Yahyaee SA, Ali BR. Hertecant JL, et al. Among authors: ben rebeh i. Eur J Med Genet. 2012 Dec;55(12):671-6. doi: 10.1016/j.ejmg.2012.08.001. Epub 2012 Aug 16. Eur J Med Genet. 2012. PMID: 22960500

5

Identification of mutations underlying 20 inborn errors of metabolism in the United Arab Emirates population.

Ben-Rebeh I, Hertecant JL, Al-Jasmi FA, Aburawi HE, Al-Yahyaee SA, Al-Gazali L, Ali BR. Ben-Rebeh I, et al. Genet Test Mol Biomarkers. 2012 May;16(5):366-71. doi: 10.1089/gtmb.2011.0175. Epub 2011 Nov 22. Genet Test Mol Biomarkers. 2012. PMID: 22106832 Free PMC article.

6

Endoplasmic reticulum quality control is involved in the mechanism of endoglin-mediated hereditary haemorrhagic telangiectasia.

Ali BR, Ben-Rebeh I, John A, Akawi NA, Milhem RM, Al-Shehhi NA, Al-Ameri MM, Al-Shamisi SA, Al-Gazali L. Ali BR, et al. Among authors: ben rebeh i. PLoS One. 2011;6(10):e26206. doi: 10.1371/journal.pone.0026206. Epub 2011 Oct 14. PLoS One. 2011. PMID: 22022569 Free PMC article.

7

Reinforcement of a minor alternative splicing event in MYO7A due to a missense mutation results in a mild form of retinopathy and deafness.

Ben Rebeh I, Morinière M, Ayadi L, Benzina Z, Charfedine I, Feki J, Ayadi H, Ghorbel A, Baklouti F, Masmoudi S. Ben Rebeh I, et al. Mol Vis. 2010 Sep 30;16:1898-906. Mol Vis. 2010. PMID: 21031134 Free PMC article.

8

Mutation in gap and tight junctions in patients with non-syndromic hearing loss.

Belguith H, Tlili A, Dhouib H, Ben Rebeh I, Lahmar I, Charfeddine I, Driss N, Ghorbel A, Ayadi H, Masmoudi S. Belguith H, et al. Among authors: ben rebeh i. Biochem Biophys Res Commun. 2009 Jul 17;385(1):1-5. doi: 10.1016/j.bbrc.2009.02.125. Epub 2009 Feb 28. Biochem Biophys Res Commun. 2009. PMID: 19254696

9

Identification of candidate regions for a novel Usher syndrome type II locus.

Ben Rebeh I, Benzina Z, Dhouib H, Hadjamor I, Amyere M, Ayadi L, Turki K, Hammami B, Kmiha N, Kammoun H, Hakim B, Charfedine I, Vikkula M, Ghorbel A, Ayadi H, Masmoudi S. Ben Rebeh I, et al. Mol Vis. 2008 Sep 19;14:1719-26. Mol Vis. 2008. PMID: 18806881 Free PMC article.

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