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Journal of Autoimmunity|July 9, 2004
Analysis of MHC genes in a Tunisian isolate with autoimmune thyroid diseases: implication of TNF -308 gene polymorphismNoura Bougacha-Elleuch, Ahmed Rebai, Mouna Mnif, et al.
Indian Journal of Endocrinology and Metabolism|January 2, 2014
The effects of an exercise training program on body composition and aerobic capacity parameters in Tunisian obese childrenSofien Regaieg, Nadia Charfi, Mahdi Kamoun, et al.
Indian Journal of Endocrinology and Metabolism|January 2, 2014
Hyperthyroidism: A rare cause of pulmonary embolism: Report of two casesSonia Grine, Nadia Charfi, Mahdi Kamoun, et al.
Biochemical and Biophysical Research Communications|March 6, 2007
Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseasesEmna Mkaouar-Rebai, Abdelaziz Tlili, Saber Masmoudi, et al.
Molecular Genetics & Genomic Medicine|May 13, 2020
The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetesMouna Tabebi, Wajdi Safi, Rahma Felhi, et al.
La Tunisie Medicale|November 16, 2018
Fahr's syndrome in Southern Tunisia: A broad spectrum of clinical and etiological featuresSahar El Aoud, Mouna Elleuch, Nadia Charfi, et al.
The Pan African Medical Journal|January 11, 2019
[Cardiovascular and metabolic impact of glucocorticoid substitution therapy in patients with Addison's disease]Dhoha Ben Salah, Nadia Charfi, Mouna Elleuch, et al.
Cytokine|June 24, 2008
A potential role of TNFR gene polymorphisms in autoimmune thyroid diseases in the Tunisian populationMaha Kammoun-Krichen, Noura Bougacha-Elleuch, Kaouthar Makni, et al.
Biochemical and Biophysical Research Communications|July 5, 2011
The mitochondrial ND1 m.3337G>A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathyNajla Mezghani, Mouna Mnif, Emna Mkaouar-Rebai, et al.
Iranian Journal of Allergy, Asthma, and Immunology|April 5, 2020
Successful Treatment of Insulin Allergy with Desensitization Therapy: A Case Report and Literature ReviewHamza Elfekih, Faten Hadjkacem, Mouna Elleuch, et al.
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