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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.
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
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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.
Journal articles
pasteur-01375143v1
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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.
Journal articles
pasteur-01374983v1
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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.
Journal articles
pasteur-01375028v1
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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.
Journal articles
hal-01513653v1
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