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Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.

Leila Chaouch , Emna Talbi , Imen Moumni , Arij Ben Chaabene , Miniar Kalai , et al.
Disease Markers, 2013, 35 (2), pp.67-72. ⟨10.1155/2013/173474⟩
Journal articles pasteur-01382164v1
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La place des gènes non globine dans la modulation du syndrome drépanocytaire

Leila Chaouch
Hématologie. Université de Tunis El Manar (Tunisie), 2012. Français. ⟨NNT : ⟩
Theses tel-03540224v1

Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia.

Leila Chaouch , Yossra Said , Imen Moumni , Imen Mahjoubi , Arij Ben Chaabene , et al.
Annales de Biologie Clinique, 2012, 70 (6), pp.702-6. ⟨10.1684/abc.2012.0743⟩
Journal articles pasteur-01375143v1

rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients

Leila Chaouch , Imen Moumni , Houyem Ouragini , Imen Darragi , Miniar Kalai , et al.
Hematology, 2016, 21 (7), pp.425-429. ⟨10.1080/10245332.2015.1107275⟩
Journal articles pasteur-01374983v1

Genetic polymorphism of cytochrome P450 2E1 and the risk of nasopharyngeal carcinoma

Arij Ben Chaaben , Hajer Abaza , Hayet Douik , Leila Chaouch , Fayza Ayari , et al.
Bulletin du Cancer, 2015, 102 (12), pp.967-972. ⟨10.1016/j.bulcan.2015.09.013⟩
Journal articles pasteur-01375028v1

The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients

Miniar Kalai , Marwa Dridi , Leila Chaouch , Imen Moumni , Houyem Ouragini , et al.
Hematology, 2017, 22 (3), pp.178-182. ⟨10.1080/10245332.2016.1253253⟩
Journal articles hal-01513653v1