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Journal of Pediatric Hematology/Oncology|January 23, 2013
Cytogenetic assessment of Fanconi anemia in children with aplastic anemia in TunisiaFaten Talmoudi, Lobna Kammoun, Nizar Benhalim, et al.Journal of Clinical Immunology|January 15, 2013
Clinical, immunological and genetic findings of a large tunisian series of major histocompatibility complex class II deficiency patientsImen Ben-Mustapha, Khaoula Ben-Farhat, Naouel Guirat-Dhouib, et al.Frontiers in Genetics|March 8, 2021
FANCA Gene Mutations in North African Fanconi Anemia PatientsAbir Ben Haj Ali, Olfa Messaoud, Sahar Elouej, et al.Immunogenetics|November 8, 2015
Novel and recurrent AID mutations underlie prevalent autosomal recessive form of HIGM in consanguineous patientsHanen Ouadani, Imen Ben-Mustapha, Meriem Ben-ali, et al.Frontiers in Immunology|March 13, 2026
Predictive factors for severity and poor treatment response in children with Evans syndrome: A retrospective cohort studyMonia Ben Khaled, Marwa Ben Ayed, Zaid Zaroui, et al.Comptes Rendus Biologies|March 30, 2013
Differentiation of Fanconi anemia and aplastic anemia using mitomycin C test in TunisiaFaten Talmoudi, Olfa Kilani, Wiem Ayed, et al.Frontiers in Immunology|January 27, 2023
Diagnostic challenge in a series of eleven patients with hyper IgE syndromesRoukaya Yaakoubi, Najla Mekki, Imen Ben-Mustapha, et al.La Tunisie Medicale|February 13, 2019
Primary Immunodeficiencies: Epidemiology in the MaghrebAhmed Aziz Bousfiha, Abderrrahmane Errami, Leila Jeddane, et al.Journal of Clinical Immunology|November 8, 2019
Genetic Approaches for Definitive Diagnosis of Agammaglobulinemia in Consanguineous FamiliesMeriem Ben-Ali, Nadia Kechout, Najla Mekki, et al.Molecular Genetics & Genomic Medicine|April 2, 2014
High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosisAhlem Amouri, Faten Talmoudi, Olfa Messaoud, et al.Pageof 6