Search Results - "Chaabene, Arij Ben"

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

“…The skeletal manifestations of sickle cell disease are the result of changes in bone and bone marrow caused by chronic tissue hypoxia that is exacerbated by…”
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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

“…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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Implication of genetic variation at the promoter and exon1 of UGT1A1 in occurrence of cholelithiasis in Tunisia by Chaouch, Leila, Said, Yossra, Moumni, Imen, Mahjoubi, Imen, Chaabene, Arij Ben, Darragi, Imen, Ghanem, Abderraouf, Abbes, Salem

“…Bilirubin is conjugated with glucoronic acid in the liver by UDP-glucuronosyltransferase 1A1 (UGT1A1). Polymorphisms at the promoter region or exon1 of UGT1A1…”
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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

“…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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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

“…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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Phenotypic and molecular changes of hemoglobinopathies in cancer by Abaza, Hajer, Gara, Yosr, Ben Chaabene, Arij, Douik, Hayet, Harzallah, Latifa, Boussen, Hamouda, Guemira, Fethi

“…The abnormalities of the haemoglobin divide into qualitative abnormalities and quantitative abnormalities. This variant contains polymorphisms often useful as…”
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