| Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome F Haddad, N Trabelsi, L Chaouch, I Darragi, M Oueslati, I Boudriga, ... Hemoglobin 41 (2), 147-150, 2017 | 5 | 2017 |
| Enhanced eryptosis in glucose-6-phosphate dehydrogenase deficiency G Bouguerra, K Talbi, N Trabelsi, D Chaouachi, I Boudriga, S Abbès, ... Cell Physiol Biochem 55 (6), 761-772, 2021 | 4 | 2021 |
| Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among Tunisians N Trabelsi, G Bouguerra, F Haddad, M Ouederni, I Darragi, I Boudrigua, ... Cellular Physiology and Biochemistry 55 (1), 117-129, 2021 | 1 | 2021 |
| 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 SM Ghaber, N Trabelsi, ML Salem, F Haddad, A Abba, I Darragi, S Abbes Hemoglobin 42 (1), 7-10, 2018 | 1 | 2018 |
| P1549: NOVEL SLC4A1 GENE MUTATIONS IN HEREDITARY SPHEROCYTOSIS BAND 3 PROTEIN-DEFICIENT TUNISIAN PATIENTS N TRABELSI, I Kraiem, S Menif, S Abbes HemaSphere 6, 1430-1431, 2022 | | 2022 |
| Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia N Trabelsi, L Chaouch, F Haddad, M Jaouani, E Barkaoui, I Darragi, ... European Journal of Medical Genetics 64 (2), 104139, 2021 | | 2021 |
| ERYTHROCYTE MEMBRANE SCRAMBLING BY PHOSPHATIDYLSERINE EXTERNALIZATION IN GLUCOSE-6-PHOSPHATE-DEFICIENT PATIENTS. G BOUGERRA, K TALBI, N TRABELSI, F HADDAD, D CHAOUACHI, ... Archives de l'Institut Pasteur de Tunis 97, 2020 | | 2020 |
