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Page 1
Predominance of the Rare EGFR Mutation p.L861Q in Tunisian Patients with Non-Small Cell Lung Carcinoma.
Abdelmaksoud-Dammak R, Ammous-Boukhris N, Saadallah-Kallel A, Charfi S, Khemiri S, Khemakhem R, Kallel N, Ben Kridis-Rejeb W, Sallemi-Boudawara T, Khanfir A, Yangui I, Daoud J, Mokdad-Gargouri R. Abdelmaksoud-Dammak R, et al. Among authors: saadallah kallel a. Genes (Basel). 2022 Aug 22;13(8):1499. doi: 10.3390/genes13081499. Genes (Basel). 2022. PMID: 36011410 Free PMC article.
Angiotensin-converting-enzyme gene insertion-deletion polymorphism and renin angiotensin aldosterone system activity in different phenotypes of polycystic ovary syndrome.
Chaabouni K, Saadallah-Kallel A, Ben Brahim S, Chaabane K, Frikha M, Mnif M, Keskes L, Abdelhedi F, Ayadi F. Chaabouni K, et al. Among authors: saadallah kallel a. Heliyon. 2024 Nov 16;10(22):e40411. doi: 10.1016/j.heliyon.2024.e40411. eCollection 2024 Nov 30. Heliyon. 2024. PMID: 39641077 Free PMC article.
Lower p66Shc promoter methylation in subjects with chronic renal failure.
Hamdi R, Saadallah-Kallel A, Ferchichi-Trimeche S, Mokdad-Gargouri R, Miled A, Benarba B. Hamdi R, et al. Among authors: saadallah kallel a. PLoS One. 2021 Sep 16;16(9):e0257176. doi: 10.1371/journal.pone.0257176. eCollection 2021. PLoS One. 2021. PMID: 34529688 Free PMC article.