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La Tunisie Medicale|November 26, 2009
[Splenectomy in hereditary hemolytic anemia: 82 Tunisian cases]Raouf Hafsia, Sami Zriba, Emna Gouider, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|June 15, 2026
Beyond Body Weight: Biological and Clinical Determinants of Factor VIII Pharmacokinetics in Tunisian PatientsSameh Neji, Ons Ghali, Maha Said, et al.La Tunisie Medicale|February 8, 2008
[Hemoglobin O Arab: about 20 cases]Raouf Hafsia, Emna Gouider, Sinda Ben Moussa, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 9, 2026
Genetic characterization of Glanzmann thrombasthenia: insights from novel igta2b mutations in a Tunisian patient cohortHajer Elmahmoudi, Nesrine Kerkeni, Temim Deli, et al.Annales De Biologie Clinique|August 24, 2021
[Contribution and limits of CD157 in the detection of the paroxysmal nocturnal hemoglobinuria clone: a case report]Sarra Bahroun, Fatma Ben Lakhal, Wijdene ElBorgi, et al.Journal of Medical Virology|October 22, 2014
Hepatitis E virus seroprevalence among hemodialysis and hemophiliac patients in Tunisia (North Africa)Yousr Ben-Ayed, Hela Hannachi, Nissaf Ben-Alaya-Bouafif, et al.Annals of Hematology|April 30, 2008
A first case of congenital TTP on the African continent due to a new homozygous mutation in the catalytic domain of ADAMTS13Sara C Meyer, Ramzi Jeddi, Balkis Meddeb, et al.Journal of Hematology|April 18, 2020
The Glanzmann's Thrombasthenia in Tunisia: A Cohort StudyHejer Elmahmoudi, Meriem Achour, Nejla Belhedi, et al.Annales De Biologie Clinique|December 18, 2013
[Immunophenotyping of B chronic lymphoproliferative syndromes (CLL excluded): confrontation with the histology]Wijden El Borgi, Nawel Ben Salah, Fatma Ben Lakhal, et al.La Tunisie Medicale|February 20, 2016
Monocentric study of Willebrand's disease in Tunisia: assets and difficultiesFatma Ben Lakhal, Wijdene El Borgi, Emna Gouider, et al.Pageof 5