Khelil AH[au] - Search Results

Year	Number of Results
2003	1
2009	1
2010	3
2011	4
2012	1
2013	2
2014	1
2015	1
2019	1
2020	1
2023	0

1

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: khelil ah. 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 Review.

2

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: khelil ah. 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.

3

Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?

Daimi H, Khelil AH, Neji A, Ben Hamda K, Maaoui S, Aranega A, Be Chibani J, Franco D. Daimi H, et al. Among authors: khelil ah. Biomed J. 2019 Aug;42(4):252-260. doi: 10.1016/j.bj.2019.03.003. Epub 2019 Sep 12. Biomed J. 2019. PMID: 31627867 Free PMC article.

4

Polymorphism of C3 complement in association with myocardial infarction in a sample of central Tunisia.

Leban N, Jraba K, Chalghoum A, Hassine S, Elhayek D, Denden S, Lakhdhar R, Maatoug F, Gamra H, Braham H, Ben Chibani J, Khelil AH. Leban N, et al. Among authors: khelil ah. Diagn Pathol. 2013 Jun 13;8:93. doi: 10.1186/1746-1596-8-93. Diagn Pathol. 2013. PMID: 23764154 Free PMC article.

5

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: khelil ah. Adv Clin Exp Med. 2020 Apr;29(4):423-429. doi: 10.17219/acem/116750. Adv Clin Exp Med. 2020. PMID: 32330377 Free article.

6

Novel ATP6V0A4 mutation described in a Tunisian patient with distal renal tubular acidosis.

El Hayek D, Bouzidi H, Pérez de Nanclares G, Soua H, Chibani JB, Ariceta G, Castaño L, Khelil AH. El Hayek D, et al. Among authors: khelil ah. Clin Nephrol. 2014 Feb;81(2):142-5. doi: 10.5414/CN107505. Clin Nephrol. 2014. PMID: 22854161

7

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: khelil ah. 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.

8

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: khelil ah. 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.

9

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: khelil ah. 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

10

PCR-based screening for the most prevalent alpha 1 antitrypsin deficiency mutations (PI S, Z, and Mmalton) in COPD patients from Eastern Tunisia.

Denden S, Lakhdar R, Keskes NB, Hamdaoui MH, Chibani JB, Khelil AH. Denden S, et al. Among authors: khelil ah. Biochem Genet. 2013 Oct;51(9-10):677-85. doi: 10.1007/s10528-013-9597-6. Epub 2013 May 11. Biochem Genet. 2013. PMID: 23666394

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