Search Results - "Boudrigua, Imen"

Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians by Trabelsi, Nawel, Bouguerra, Ghada, Haddad, Faten, Ouederni, Monia, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Barmat, Mbarka, Fouzai, Chaker, Bejaoui, Mohamed, Menif, Samia, Kraiem, Imen, Abbes, Salem

“…Hereditary Spherocytosis (HS) is the most common erythrocyte membrane disorder causing hemolytic anemia. The wide heterogeneity of both clinical and laboratory…”
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PB2558: REFERENCE VALUES FOR METHEMOGLOBIN LEVEL AND NADH-CYTOCHROME B5 REDUCTASE ACTIVITY IN TUNISIAN POPULATION by Bouatrous, Emna, Chaouachi, Dorra, Imen, Boudrigua, Samia, Menif, Houyem, Ouragini

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PB2558: REFERENCE VALUES FOR METHEMOGLOBIN LEVEL AND NADH‐CYTOCHROME B5 REDUCTASE ACTIVITY IN TUNISIAN POPULATION by Bouatrous, Emna, Chaouachi, Dorra, Imen, Boudrigua, Samia, Menif, Houyem, Ouragini

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New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level by Chaouch, Leila, Sellami, Houssem, Kalai, Miniar, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Abbes, Salem, Mnif, Samia

“…The 5' upstream region of the HBG1 gene plays a very important role in the expression of fetal hemoglobin (HbF). In contrast, increased HbF levels can inhibit…”
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Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia by Trabelsi, Nawel, Chaouch, Leila, Haddad, Faten, Jaouani, Mouna, Barkaoui, Emna, Darragi, Imen, Chaouachi, Dorra, Boudrigua, Imen, Menif, Samia, Abbes, Salem

“…Unconjugated hyperbilirubinemia (UCB) is a feature of Gilbert's syndrome (GS) and Crigler-Najjar's syndrome (CNS), which are two hereditary defects in…”
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rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients by Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Kalai, Miniar, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

“…Fetal hemoglobin (HbF) modulates the phenotype of sickle cell anemia (SCA) by inhibiting deoxy sickle hemoglobin (HbS) polymerization. HbF genes are…”
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The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients by Kalai, Miniar, Dridi, Marwa, Chaouch, Leila, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Mellouli, Fethi, Bejaoui, Mohamed, Abbes, Salem

“…Mediators of adhesion become a potential new target for pharmacological therapy to struggle the complications of sickle cell disease (SCD). Several mechanisms…”
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Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1 by Chaouch, Leila, Kalai1, Miniar, Darragi, Imen, Boudrigua, Imen, Chaouachi, Dorra, Ammar, Slim Ben, Mellouli, F, Bjaoui, M, Abbes, Salem

“…Hyperbilirubinemia is often observed in chronic hemolysis and results in the formation of pigment cholelithiasis that could be increased by the presence of…”
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Association of rs1319868, rs1567811 and rs8041224 of IGF1R gene with infection among sickle cell anemia Tunisian patients by Ben Sassi, Mouna, Chaouch, Leila, Kalai, Miniar, Moumni, Imen, Ouragini, Houyem, Darragi, Imen, Chaouachi, Dorra, Boudrigua, Imen, Hafsia, Raouf, Abbes, Salem

“…Sickle cell anemia (SCA) is characterized by variable patterns of clinical expression. Polymorphisms linked to different genes have been associated with…”
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