Slimani A - Search Results

1

Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patients.

Slimani A, Jelassi A, Jguirim I, Najah M, Rebhi L, Omezzine A, Maatouk F, Hamda KB, Kacem M, Rabès JP, Abifadel M, Boileau C, Rouis M, Slimane MN, Varret M. Slimani A, et al. Atherosclerosis. 2012 May;222(1):158-66. doi: 10.1016/j.atherosclerosis.2012.02.018. Epub 2012 Feb 19. Atherosclerosis. 2012. PMID: 22417841

2

Effect of a splice site mutation in LDLR gene and two variations in PCSK9 gene in Tunisian families with familial hypercholesterolaemia.

Jelassi A, Slimani A, Jguirim I, Najah M, Maatouk F, Varret M, Slimane MN. Jelassi A, et al. Among authors: slimani a. Ann Clin Biochem. 2011 Jan;48(Pt 1):83-6. doi: 10.1258/acb.2010.010087. Epub 2010 Nov 29. Ann Clin Biochem. 2011. PMID: 21115573

3

Moderate phenotypic expression of familial hypercholesterolemia in Tunisia.

Jelassi A, Slimani A, Jguirim I, Najah M, Abid A, Boughamoura L, Mzid J, Fkih M, Maatouk F, Rouis M, Varret M, Slimane MN. Jelassi A, et al. Among authors: slimani a. Clin Chim Acta. 2010 May 2;411(9-10):735-8. doi: 10.1016/j.cca.2010.02.008. Epub 2010 Feb 6. Clin Chim Acta. 2010. PMID: 20144596

4

Genomic characterization of two deletions in the LDLR gene in Tunisian patients with familial hypercholesterolemia.

Jelassi A, Slimani A, Rabès JP, Jguirim I, Abifadel M, Boileau C, Najah M, M'rabet S, Mzid J, Slimane MN, Varret M. Jelassi A, et al. Among authors: slimani a. Clin Chim Acta. 2012 Dec 24;414:146-51. doi: 10.1016/j.cca.2012.08.002. Epub 2012 Aug 14. Clin Chim Acta. 2012. PMID: 22910581

5

Autosomal dominant hypercholesterolemia: needs for early diagnosis and cascade screening in the tunisian population.

Jelassi A, Najah M, Slimani A, Jguirim I, Slimane MN, Varret M. Jelassi A, et al. Among authors: slimani a. Curr Genomics. 2013 Mar;14(1):25-32. doi: 10.2174/138920213804999200. Curr Genomics. 2013. PMID: 23997648 Free PMC article.

6

Effect of E670G Polymorphism in PCSK9 Gene on the Risk and Severity of Coronary Heart Disease and Ischemic Stroke in a Tunisian Cohort.

Slimani A, Harira Y, Trabelsi I, Jomaa W, Maatouk F, Hamda KB, Slimane MN. Slimani A, et al. J Mol Neurosci. 2014 Jun;53(2):150-7. doi: 10.1007/s12031-014-0238-2. Epub 2014 Mar 6. J Mol Neurosci. 2014. PMID: 24599757

7

PCSK9 polymorphism in a Tunisian cohort: identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease risk.

Slimani A, Hrira MY, Najah M, Jomaa W, Maatouk F, Hamda KB, Abifadel M, Rabès JP, Boileau C, Rouis M, Slimane MN, Varret M. Slimani A, et al. Mol Cell Probes. 2015 Feb;29(1):1-6. doi: 10.1016/j.mcp.2014.09.001. Epub 2014 Sep 18. Mol Cell Probes. 2015. PMID: 25239117

8

+294T/C polymorphism in the PPAR-delta gene is associated with risk of coronary artery disease in normolipidemic Tunisians.

Jguirim-Souissi I, Jelassi A, Hrira Y, Najah M, Slimani A, Addad F, Hassine M, Hamda KB, Maatouk F, Rouis M, Slimane MN. Jguirim-Souissi I, et al. Among authors: slimani a. Genet Mol Res. 2010 Jul 13;9(3):1326-33. doi: 10.4238/vol9-3gmr831. Genet Mol Res. 2010. PMID: 20645257 Free article.

9

[Association between variants of lipoprotein lipase and coronary heart disease in a Tunisian population].

Jelassi A, Jguirim I, Slimani A, Najah M, Hamda KB, Addad F, Hassine M, Maatouk F, Varret M, Slimane MN. Jelassi A, et al. Among authors: slimani a. Pathol Biol (Paris). 2012 Jun;60(3):180-4. doi: 10.1016/j.patbio.2011.04.003. Epub 2011 May 28. Pathol Biol (Paris). 2012. PMID: 21621348 French.

10

Matrix metalloproteinase-1 and matrix metalloproteinase-12 gene polymorphisms and the outcome of coronary artery disease.

Jguirim-Souissi I, Jelassi A, Slimani A, Addad F, Hassine M, Hamda KB, Najah M, Maatouk F, Rouis M, Slimane MN. Jguirim-Souissi I, et al. Among authors: slimani a. Coron Artery Dis. 2011;22(6):388-93. doi: 10.1097/MCA.0b013e3283478d40. Coron Artery Dis. 2011. PMID: 21606841

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