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Hematology (Amsterdam, Netherlands)|November 22, 2016
The role of rs1984112_G at CD36 gene in increasing reticulocyte level among sickle cell disease patientsMiniar Kalai, Marwa Dridi, Leila Chaouch, et al.Human Mutation|June 8, 2026
Mutation Spectrum of Hemoglobinopathies in TunisiaImen Moumni, Khouloud Khalfaoui, Mariem Chebbi, et al.International Orthopaedics|July 15, 2023
Incidence and risk factors for osteonecrosis of the femoral head in five hundred and ten sickle cell disease paediatric patientsMonia Ouederni, Hatem Rouag, Ilhem Ben Fraj, et al.Annals of the New York Academy of Sciences|December 2, 2011
Primary immunodeficiencies in highly consanguineous North African populationsMohamed-Ridha Barbouche, Nermeen Galal, Imen Ben-Mustapha, et al.Blood Cells, Molecules & Diseases|July 15, 2019
Predictors of autoimmune hemolytic anemia in beta-thalassemia patients with underlying red blood cells autoantibodiesMonia Ben Khaled, Monia Ouederni, Nessrine Sahli, et al.Clinical and Molecular Allergy : CMA|April 25, 2012
Oral HPV infection and MHC class II deficiency (A study of two cases with atypical outcome)Naouel Guirat-Dhouib, Yemen Baccar, Imène Ben Mustapha, et al.Journal of Cellular and Molecular Medicine|October 13, 2025
Circulating Erythrocyte- and Endothelial-Derived Microvesicles as Biomarkers of Hemolysis and Clinical Severity in Sickle Cell DiseaseKhouloud Khalfaoui, Mariem Chebbi, Oussema Souiai, et al.Annals of Hematology|March 5, 2025
Sideroblastic anemia in children: challenges in diagnosis and management in three casesSamia Rekaya, Ilhem Ben Fraj, Rym Hamdi, et al.European Journal of Pediatrics|April 8, 2006
Kaposi's sarcoma in a child with Wiskott-Aldrich syndromeCapucine Picard, Fethi Mellouli, Renan Duprez, et al.Molecular Immunology|July 14, 2017
A founder mutation underlies a severe form of phosphoglutamase 3 (PGM3) deficiency in Tunisian patientsLeila Ben-Khemis, Najla Mekki, Imen Ben-Mustapha, et al.Pageof 6