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Page 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. Among authors: rouis m. Atherosclerosis. 2012 May;222(1):158-66. doi: 10.1016/j.atherosclerosis.2012.02.018. Epub 2012 Feb 19. Atherosclerosis. 2012. PMID: 22417841
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: rouis m. 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
Plasma metalloproteinase-12 and tissue inhibitor of metalloproteinase-1 levels and presence, severity, and outcome of coronary artery disease.
Jguirim-Souissi I, Jelassi A, Addad F, Hassine M, Najah M, Ben Hamda K, Maatouk F, Ben Farhat M, Bouslema A, Rouis M, Slimane MN. Jguirim-Souissi I, et al. Among authors: rouis m. Am J Cardiol. 2007 Jul 1;100(1):23-7. doi: 10.1016/j.amjcard.2007.01.069. Epub 2007 May 7. Am J Cardiol. 2007. PMID: 17599435 Clinical Trial.
88 results