Phenotypic and molecular genetic analysis of Pyruvate Kinase deficiency in a Tunisian family von Mouna, Jaouani, Nadia, Hamdi, Leila, Chaouch, Miniar, Kalai, Fethi, Mellouli, Imen, Darragi, Imen, Boudriga, Dorra, Chaouachi, Mohamed, Bejaoui, Salem, Abbes

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Association between rs267196 and rs267201 of BMP6 gene and osteonecrosis among sickle cell aneamia patients von Chaouch, Leila, Kalai, Miniar, Jbara, Manel Ben, Chaabene, Arij Ben, Darragi, Imen, Chaouachi, Dorra, Mallouli, Fethi, Hafsia, Raouf, Ghanem, Abderraouf, Abbes, Salem

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Gilbert syndrome acts as a risk factor of developing gallstone among β hemoglobinopathy Tunisian patients von Chaouch, Leila, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Hafsia, Raouf, Ben Ammar, Slim, Abbes, Salem

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients von Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Kalai, Miniar, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients von Kalai, Miniar, Dridi, Marwa, Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Mellouli, Fethi, Bejaoui, Mohamed, Abbes, Salem

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Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1 von Chaouch, Leila, Kalail, Miniar, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Ammar, Slim Ben, Mellouli, F., Bjaoui, M., Abbes, Salem

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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients von Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Kalai, Miniar, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

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Early Complication in Sickle Cell Anemia Children due to A(TA)nTAA Polymorphism at the Promoter of UGT1A1 Gene von Abbes, Salem, Ghanem, Abderraouf, Chaouachi, Dorra, Kalai, Miniar, Ben Chaabene, Arij, Moumni, Imen, Talbi, Emna, Chaouch, Leila, Mallouli, Fethi

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Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene von Chaouch, Leila, Talbi, Emna, Moumni, Imen, Ben Chaabene, Arij, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Ghanem, Abderraouf, Abbes, Salem

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Early complication in Sickle Cell Anemia children due to A(TA)_n TAA polymorphism at the promoter of UGT1A1 gene von Chaouch, Leila, Talbi, Emna, Moumni, Imen, Ben Chaabene, Arij, Kalai, Miniar, Chaouachi, Dorra, Mallouli, Fethi, Ghanem, Abderraouf, Abbes, Salem

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Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients von Ben Sassi, Mouna, Chaouch, Leila, Kalai, Miniar, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

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Frequency of three polymorphisms of the CCL5 gene (rs2107538, rs2280788 and rs2280789) and their implications for the phenotypic expression of sickle cell anemia in Tunisia von Kalai, M, Chaouch, L, Mansour, I B, Hafsia, R, Ghanem, A, Abbes, S

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