Search Results - "Mallouli, Fethi"

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

    Published in Tunisie Medicale (01-04-2015)
    “…As a result of chronic hemolysis, hyperbilirubinemia is often observed, leading to the formation of pigment cholelithiasis which could be busted by the…”
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    Journal Article
  3. 3

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

    Published in Disease markers (2013)
    “…Aim. To determine the implication of the polymorphism, namely, A(TA)nTAA of UGT1A1 in lithogenesis for the first time in Tunisia among sickle cell anemia (SCA)…”
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    Journal Article
  4. 4

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

    Published in Disease markers (25-04-2013)
    “…AIM: To determine the implication of the polymorphism namely A(TA)nTAA of UGT1A1 in lithogenesis for the first time in Tunisia among sickle cell anemia (SCA)…”
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    Journal Article
  5. 5

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

    Published in Disease markers (25-04-2013)
    “…AIM: To determine the implication of the polymorphism namely A(TA)nTAA of UGT1A1 in lithogenesis for the first time in Tunisia among sickle cell anemia (SCA)…”
    Get full text
    Journal Article