1. A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]. (April 2014) Authors: Moumni, Imen; Zorai, Amine; Mahjoub, Sonia; Mosbahi, Ikbel; Chaouechi, Dorra; Benromdhane, Neila; Abbes, Salem Journal: Hemoglobin Issue: Volume 38:Number 2(2014) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Association of genetic variation in IKZF1, ARID5B, CDKN2A, and CEBPE with the risk of acute lymphoblastic leukemia in Tunisian children and their contribution to racial differences in leukemia incidence. (2nd April 2016) Authors: Gharbi, Hanene; Ben Hassine, Islem; Soltani, Ismail; Safra, Ines; Ouerhani, Slah; Bel Haj Othmen, Hind; Teber, Mouheb; Farah, Ahlem; Amouri, Hassiba; Toumi, Nourel Houda; Abdennebi, Salima; Abbes, Salem; Menif, Samia Journal: Pediatric hematology and oncology Issue: Volume 33:Number 3(2016) Page Start: 157 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Downregulation of miR-451 in Tunisian chronic myeloid leukemia patients: potential implication in imatinib resistance. Issue 4 (21st April 2017) Authors: Soltani, Ismael; Douzi, Kais; Gharbi, Hanen; Benhassine, Islem; Teber, Mouheb; Amouri, Hassiba; Ben Hadj Othman, Hind; Farrah, Ahlem; Ben Lakhel, Raihane; Abbes, Salem; Menif, Samia Journal: Hematology Issue: Volume 22:Issue 4(2017) Page Start: 201 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby. Issue 8 (November 2021) Authors: Bouatrous, Emna; Nouira, Sonia; Ben Khaled, Monia; Ouederni, Monia; Abbes, Salem; Menif, Samia; Ouragini, Houyem Journal: Journal of pediatric hematology/oncology Issue: Volume 43:Issue 8(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. 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) ↗
6. 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) ↗
7. Haplotype Map of Sickle Cell Anemia in Tunisia. (2nd July 2014) Authors: Moumni, Imen; Ben Mustapha, Maha; Sassi, Sarra; Zorai, Amine; Ben Mansour, Ikbel; Douzi, Kais; Chouachi, Dorra; Mellouli, Fethi; Bejaoui, Mohamed; Abbes, Salem Other Names: Lapaire Olav Academic Editor. Journal: Disease markers Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. 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) ↗
9. 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) ↗
10. 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) ↗