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La Tunisie Medicale|April 27, 2010
[Thalassemia intermedia: 36 cases]Raouf Hafsia, Naouel Ben Salah, Emna Hafhouf, et al.Blood Transfusion = Trasfusione Del Sangue|May 11, 2022
Efficacy and safety of von Willebrand factor concentrate almost devoid of factor VIII (Wilfactin®) in paediatric patients under 6 years of age with severe von Willebrand diseaseEmna Gouider, Anna Klukowska, Philip Maes, et al.La Tunisie Medicale|December 19, 2012
[Quality of life during menstruation in women with an inherited bleeding disorder: report of 31 cases]Anis Fadhlaoui, Mohamed Khrouf, Amel Chelbi, et al.Diagnostic Pathology|June 21, 2011
Factor VIII haplotypes frequencies in Tunisian hemophiliacs AHejer Elmahmoudi, Nejla Belhedi, Asma Jlizi, et al.Laboratory Medicine|February 19, 2022
Acquired FVII Deficiency and Acute Myeloid Leukemia: A Case Report and Literature ReviewEmna Hammami, Wijden El Borgi, Fatma Ben Lakhal, et al.Medical Oncology (Northwood, London, England)|October 29, 2025
Ex vivo evaluation of Allium sativum extract on acute myeloid leukemia cells and leukemia stem cell populationsMohamed Abdelkarim, Rachid Kharrat, Fatma Ben Lakhal, et al.Annales De Biologie Clinique|April 23, 2020
Haemodialysis Tunisian patient with acquired factor V inhibitor associated to arteriovenous shunt thrombosisIkbel Ghachem, Wijdène El Borgi, Sarra Fekih Salem, et al.La Tunisie Medicale|July 31, 2007
[Cytology and immunophenotype feautures of 80 acute myeloid leukemia]Emna Gouider, Sameh Ayari, Selma Bouhoula, et al.Expert Review of Hematology|November 13, 2024
Global prophylaxis trends in hemophilia: a macroeconomic analysis and its association with world development indicatorsM Joseph John, Jeff Stonebraker, Aikaj Jindal, et al.La Tunisie Medicale|July 13, 2022
Factor XI deficiency: About 20 cases and literature reviewYosra Dhaha, Wijdène El Borgi, Hajer Elmahmoudi, et al.Pageof 5