1. Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1. Issue 2 (7th February 2016) Authors: Chaouch, Leila; Kalail, Miniar; Darragi, Imen; Boudrigua, Imen; Chaouachi, Dorra; Ammar, Slim Ben; Mellouli, F.; Bjaoui, M.; Abbes, Salem Journal: Hematology Issue: Volume 21:Issue 2(2016) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic link with cholelithiasis among pediatric SCA Tunisian patients: Examples of UGT1A1, SLCO1A2 and SLCO1B1. Issue 2 (7th February 2016) Authors: Chaouch, Leila; Kalai1, Miniar; Darragi, Imen; Boudrigua, Imen; Chaouachi, Dorra; Ammar, Slim Ben; Mellouli, F.; Bjaoui, M.; Abbes, Salem Journal: Hematology Issue: Volume 21:Issue 2(2016) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Hb Moscva [β24(B6)Gly→Asp (GGT>GAT), HBB: c.74G>A]: An Unstable Hemoglobin Newly Detected as a De Novo Mutation in a Mauritanian Patient. (2nd January 2018) Authors: Ghaber, Sidi M.; Trabelsi, Nawel; Salem, Mohamed L.; Haddad, Faten; Abba, Aminetou; Darragi, Imen; Abbes, Salem Journal: Hemoglobin Issue: Volume 42:Number 1(2018) Page Start: 7 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert's Syndrome. (4th March 2017) Authors: Haddad, Faten; Trabelsi, Nawel; Chaouch, Leila; Darragi, Imen; Oueslati, Meriem; Boudriga, Imen; Chaouachi, Dorra; El-Borgi, Wijdene; Hafsia, Raouf; Abbes, Salem; Ouragini, Houyem Journal: Hemoglobin Issue: Volume 41:Number 2(2017) Page Start: 147 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. New Deletion at Promoter of HBG1 Gene in Sickle Cell Disease Patients With High HbF Level. Issue 1 (January 2020) Authors: Chaouch, Leila; Sellami, Houssem; Kalai, Miniar; Darragi, Imen; Boudrigua, Imen; Chaouachi, Dorra; Abbes, Salem; Mnif, Samia Journal: Journal of pediatric hematology/oncology Issue: Volume 42:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Rapid and inexpensive detection of common HBB gene mutations in Tunisian population by high-resolution melting analysis: Implication for molecular diagnosis. Issue 2 (March 2014) Authors: Ouragini, Houyem; Haddad, Faten; Darragi, Imen; Abbes, Salem Journal: Hematology Issue: Volume 19:Issue 2(2014) Page Start: 80 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Rs11886868 and rs4671393 of BCL11A associated with HbF level variation and modulate clinical events among sickle cell anemia patients. Issue 7 (8th August 2016) Authors: Chaouch, Leila; Moumni, Imen; Ouragini, Houyem; Darragi, Imen; Kalai, Miniar; Chaouachi, Dorra; Boudrigua, Imen; Hafsia, Raouf; Abbes, Salem Journal: Hematology Issue: Volume 21:Issue 7(2016) Page Start: 425 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patients. Issue 3 (16th March 2017) Authors: Kalai, Miniar; Dridi, Marwa; Chaouch, Leila; Moumni, Imen; Ouragini, Houyem; Darragi, Imen; Boudrigua, Imen; Chaouachi, Dorra; Mellouli, Fethi; Bejaoui, Mohamed; Abbes, Salem Journal: Hematology Issue: Volume 22:Issue 3(2017) Page Start: 178 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗