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Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|March 5, 2021
Biochemical, Cellular, and Proteomic Characterization of Hereditary Spherocytosis Among TunisiansNawel Trabelsi, Ghada Bouguerra, Faten Haddad, et al.Annals of Human Biology|December 4, 2019
Consanguineous unions and endogamy in families of beta-thalassaemia patients from two Mediterranean populations: Tunisia and ItalyRamla Weslati, Monia Ouederni, Giovanbattista Ruffo, et al.Journal of Cellular Physiology|May 16, 2018
Zinc mitigates renal ischemia-reperfusion injury in rats by modulating oxidative stress, endoplasmic reticulum stress, and autophagyNajet Hadj Abdallah, Anna Baulies, Ahlem Bouhlel, et al.Journal of Pineal Research|April 5, 2013
AMPK involvement in endoplasmic reticulum stress and autophagy modulation after fatty liver graft preservation: a role for melatonin and trimetazidine cocktailMohamed Amine Zaouali, Eleonora Boncompagni, Russel J Reiter, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|June 12, 2018
The effect of zinc acexamate on oxidative stress, inflammation and mitochondria induced apoptosis in rat model of renal warm ischemiaNajet Hadj Abdallah, Anna Baulies, Ahlem Bouhlel, 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.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.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.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 11