Keskes L - Search Results

1

Association study of MICA gene polymorphisms with rheumatoid arthritis susceptibility in south Tunisian population.

Achour Y, Kammoun A, Ben Hamad M, Mahfoudh N, Chaabane S, Marzouk S, Keskes L, Gaddour L, Bahloul Z, Maalej A. Achour Y, et al. Among authors: keskes l. Int J Immunogenet. 2014 Dec;41(6):486-92. doi: 10.1111/iji.12146. Epub 2014 Sep 26. Int J Immunogenet. 2014. PMID: 25256191

2

Genetic Determinants of Methotrexate Toxicity in Tunisian Patients with Rheumatoid Arthritis: A Study of Polymorphisms Involved in the MTX Metabolic Pathway.

Chaabane S, Marzouk S, Akrout R, Ben Hamad M, Achour Y, Rebai A, Keskes L, Fourati H, Bahloul Z, Maalej A. Chaabane S, et al. Among authors: keskes l. Eur J Drug Metab Pharmacokinet. 2016 Aug;41(4):385-93. doi: 10.1007/s13318-015-0288-z. Eur J Drug Metab Pharmacokinet. 2016. PMID: 26077125

3

Novel cases of Tunisian patients with mutations in the gene encoding 17β-hydroxysteroid dehydrogenase type 3 and a founder effect.

Ben Rhouma B, Kallabi F, Mahfoudh N, Ben Mahmoud A, Engeli RT, Kamoun H, Keskes L, Odermatt A, Belguith N. Ben Rhouma B, et al. Among authors: keskes l. J Steroid Biochem Mol Biol. 2017 Jan;165(Pt A):86-94. doi: 10.1016/j.jsbmb.2016.03.007. Epub 2016 Mar 5. J Steroid Biochem Mol Biol. 2017. PMID: 26956191

4

Measurement of absolute copy number variation of Glutathione S-Transferase M1 gene by digital droplet PCR and association analysis in Tunisian Rheumatoid Arthritis population.

Achour Y, Ben Kilani MS, Ben Hamad M, Marzouk S, Mahfoudh N, Bahloul Z, Keskes L, Petit-Teixeira E, Maalej A. Achour Y, et al. Among authors: keskes l. J Clin Lab Anal. 2018 Mar;32(3):e22300. doi: 10.1002/jcla.22300. Epub 2017 Jul 13. J Clin Lab Anal. 2018. PMID: 28703442 Free PMC article.

5

Analysis of two susceptibility SNPs in HLA region and evidence of interaction between rs6457617 in HLA-DQB1 and HLA-DRB1*04 locus on Tunisian rheumatoid arthritis.

Achour Y, Ben Hamad M, Chaabane S, Rebai A, Marzouk S, Mahfoudh N, Bahloul Z, Keskes L, Maalej A. Achour Y, et al. Among authors: keskes l. J Genet. 2017 Dec;96(6):911-918. doi: 10.1007/s12041-017-0855-y. J Genet. 2017. PMID: 29321349

6

Association of hyperhomocysteinemia with genetic variants in key enzymes of homocysteine metabolism and methotrexate toxicity in rheumatoid arthritis patients.

Chaabane S, Messedi M, Akrout R, Ben Hamad M, Turki M, Marzouk S, Keskes L, Bahloul Z, Rebai A, Ayedi F, Maalej A. Chaabane S, et al. Among authors: keskes l. Inflamm Res. 2018 Aug;67(8):703-710. doi: 10.1007/s00011-018-1161-8. Epub 2018 May 23. Inflamm Res. 2018. PMID: 29796841

7

Mutations in GAA Gene in Tunisian Families with Infantile Onset Pompe Disease: Novel Mutation and Structural Modeling Investigations.

Alila-Fersi O, Aloulou H, Werteni I, Mahfoudh N, Chabchoub I, Kammoun H, Keskes L, Hachicha M, Belguith N, Fakhfakh F. Alila-Fersi O, et al. Among authors: keskes l. J Mol Neurosci. 2020 Jul;70(7):1100-1109. doi: 10.1007/s12031-020-01516-9. Epub 2020 Mar 3. J Mol Neurosci. 2020. PMID: 32125626

8

Analysis of azoospermia factor loci polymorphisms among Tunisian infertile men with varicocele.

Hadjkacem-Loukil L, Hadj Kacem H, Salem IH, Bahloul A, Keskes L, Fakhfakh F, Ayadi H. Hadjkacem-Loukil L, et al. Among authors: keskes l. Genet Test Mol Biomarkers. 2010 Sep 6. doi: 10.1089/gtmb.2010.0019. Epub 2010 Sep 6. Genet Test Mol Biomarkers. 2010. Retraction in: Genet Test Mol Biomarkers. 2011 Sep;15(9):664. doi: 10.1089/gtmb.2010.0019.ret PMID: 20818979 Retracted.

9

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.

Kallabi F, Belghuith N, Aloulou H, Kammoun T, Ghorbel S, Hajji M, Gallas S, Chemli J, Chabchoub I, Azzouz H, Ben Chehida A, Sfaihi L, Makni S, Amouri A, Keskes L, Tebib N, Ben Becher S, Hachicha M, Kamoun H. Kallabi F, et al. Among authors: keskes l. Arch Med Res. 2016 Feb;47(2):105-10. doi: 10.1016/j.arcmed.2016.04.004. Epub 2016 Apr 28. Arch Med Res. 2016. PMID: 27133709

10

Mutational screening in patients with profound sensorineural hearing loss and neurodevelopmental delay: Description of a novel m.3861A > C mitochondrial mutation in the MT-ND1 gene.

Ammar M, Tabebi M, Sfaihi L, Alila-Fersi O, Maalej M, Felhi R, Chabchoub I, Keskes L, Hachicha M, Fakhfakh F, Mkaouar-Rebai E. Ammar M, et al. Among authors: keskes l. Biochem Biophys Res Commun. 2016 Jun 10;474(4):702-708. doi: 10.1016/j.bbrc.2016.05.014. Epub 2016 May 4. Biochem Biophys Res Commun. 2016. PMID: 27155156

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