Chibani J - Search Results

1

Atypical hemolytic uremic syndrome in the Tunisian population.

Leban N, Aloui S, Touati D, Lakhdhar R, Skhiri H, Lefranc G, Achour A, Elmay M, Lopez-Trascasa M, Sanchez-Corral P, Chibani J, Haj Khelil A. Leban N, et al. Among authors: chibani j. Int Urol Nephrol. 2011 Jun;43(2):559-64. doi: 10.1007/s11255-010-9754-3. Epub 2010 May 25. Int Urol Nephrol. 2011. PMID: 20499172

2

Factor H and CFHR1 polymorphisms associated with atypical Haemolytic Uraemic Syndrome (aHUS) are differently expressed in Tunisian and in Caucasian populations.

Leban N, Abarrategui-Garrido C, Fariza-Requejo E, Amiñoso-Carbonero C, Pinto S, Chibani JB, Khelil AH, Sánchez-Corral P. Leban N, et al. Among authors: chibani jb. Int J Immunogenet. 2012 Apr;39(2):110-3. doi: 10.1111/j.1744-313X.2011.01071.x. Epub 2011 Dec 5. Int J Immunogenet. 2012. PMID: 22136554

3

Microsomal epoxide hydrolase gene polymorphisms and susceptibility to chronic obstructive pulmonary disease in the Tunisian population.

Lakhdar R, Denden S, Knani J, Leban N, Daimi H, Hassine M, Lefranc G, Chibani JB, Khelil AH. Lakhdar R, et al. Among authors: chibani jb. Genet Test Mol Biomarkers. 2010 Dec;14(6):857-63. doi: 10.1089/gtmb.2009.0168. Epub 2010 Oct 9. Genet Test Mol Biomarkers. 2010. PMID: 20932192

4

Update in chronic obstructive pulmonary disease: role of antioxidant and metabolizing gene polymorphisms.

Lakhdar R, Denden S, Kassab A, Leban N, Knani J, Lefranc G, Miled A, Chibani JB, Khelil AH. Lakhdar R, et al. Among authors: chibani jb. Exp Lung Res. 2011 Aug;37(6):364-75. doi: 10.3109/01902148.2011.580416. Epub 2011 Jul 1. Exp Lung Res. 2011. PMID: 21721950 Free article. Review.

5

Combined analysis of EPHX1, GSTP1, GSTM1 and GSTT1 gene polymorphisms in relation to chronic obstructive pulmonary disease risk and lung function impairment.

Lakhdar R, Denden S, Knani J, Leban N, Daimi H, Hassine M, Lefranc G, Chibani JB, Khelil AH. Lakhdar R, et al. Among authors: chibani jb. Dis Markers. 2011;30(5):253-63. doi: 10.3233/DMA-2011-0782. Dis Markers. 2011. PMID: 21734345 Free PMC article.

6

In silico analysis of alpha1-antitrypsin variants: The effects of a novel mutation.

Denden S, Leban N, Hayek D, Knani J, Chibani JB, Khelil AH. Denden S, et al. Among authors: chibani jb. Genet Mol Biol. 2010 Oct;33(4):633-6. doi: 10.1590/S1415-47572010005000089. Epub 2010 Dec 1. Genet Mol Biol. 2010. PMID: 21637569 Free PMC article.

7

Serum protein polymorphism among Tunisian Berbers: haptoglobin, transferrin and group-specific component subtypes, C3 and BF types.

Chibani J, Lefranc G, Constans J. Chibani J, et al. Ann Hum Biol. 1985 Sep-Oct;12(5):449-62. doi: 10.1080/03014468500008011. Ann Hum Biol. 1985. PMID: 3851637 Free article.

8

Alpha-1 antitrypsin gene polymorphism in Chronic Obstructive Pulmonary Disease (COPD).

Denden S, Khelil AH, Knani J, Lakhdar R, Perrin P, Lefranc G, Chibani JB. Denden S, et al. Among authors: chibani jb. Genet Mol Biol. 2010 Jan;33(1):23-6. doi: 10.1590/S1415-47572009005000107. Epub 2010 Mar 1. Genet Mol Biol. 2010. PMID: 21637600 Free PMC article.

9

Single nucleotide polymorphisms of SCN5A and SCN10A genes increase the risk of ventricular arrhythmias during myocardial infarction.

Foddha H, Bouzidi N, Foddha A, Chouchene S, Touhami R, Leban N, Maatoug MF, Gamra H, Ferchichi S, Chibani JB, Khelil AH. Foddha H, et al. Among authors: chibani jb. Adv Clin Exp Med. 2020 Apr;29(4):423-429. doi: 10.17219/acem/116750. Adv Clin Exp Med. 2020. PMID: 32330377 Free article.

10

Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report.

Denden S, Zorzetto M, Amri F, Knani J, Ottaviani S, Scabini R, Gorrini M, Ferrarotti I, Campo I, Chibani JB, Khelil AH, Luisetti M. Denden S, et al. Among authors: chibani jb. Orphanet J Rare Dis. 2009 Apr 15;4:12. doi: 10.1186/1750-1172-4-12. Orphanet J Rare Dis. 2009. PMID: 19368725 Free PMC article.

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