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Frontiers in Endocrinology|August 16, 2021
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical InvestigationMariam Moalla, Wajdi Safi, Maab Babiker Mansour, et al.
Frontiers in Endocrinology|April 30, 2026
Effects of a 50% versus 100% pre-prandial insulin bolus reduction to improve glycemic safety during postprandial continuous and intermittent exercise in adults with type 1 diabetes treated with multiple daily injectionsWarda Lahouel, Mouna Mnif, Mohamed Amine Bouzid, et al.
Gene|October 9, 2017
Association study of apoptosis gene polymorphisms in mitochondrial diabetes: A potential role in the pathogenicity of MDMouna Tabebi, Bodour Khabou, Hanen Boukadi, et al.
Thyroid : Official Journal of the American Thyroid Association|May 24, 2018
Thyroid Hypoplasia in Congenital Hypothyroidism Associated with Thyroid Peroxidase MutationsAthanasia Stoupa, Rim Chaabane, Manelle Guériouz, et al.
Meta Gene|January 22, 2015
A 20 year history of clinical and genetic study of thyroid autoimmunity in a Tunisian multigenerational family: Evidence for gene interactionNoura Bougacha-Elleuch, Nadia Charfi, Najla Kharrat, et al.
European Cytokine Network|September 22, 2012
IL-1β a potential factor for discriminating between thyroid carcinoma and atrophic thyroiditisMaha Kammoun-Krichen, Noura Bougacha-Elleuch, Mouna Mnif, et al.
Canadian Journal of Diabetes|July 1, 2024
Investigating the Impact of Time of Day on Glycaemia in Response to Postprandial Supramaximal Sprints in Adults With Type 1Ilyess Aouin Chaieb, Faten Hadj Kacem, Mouna Mnif, et al.
Endocrine Regulations|March 31, 2026
One genotype with a myriad of phenotypes: A family with multiple endocrine neoplasiaOumeyma Trimeche, Fatma Mnif, Fatma Abdelhedi, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|July 15, 2022
A novel thymidine phosphorylase mutation in a family with Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE): Molecular docking, dynamic simulation and computational investigationsMarwa Ammar, Wajdi Safi, Abdelaziz Tlili, et al.
European Journal of Medical Genetics|September 16, 2022
An unusual familial Xp22.12 microduplication including EIF1AX: A novel candidate dosage-sensitive gene for premature ovarian insufficiencyRim Sakka, Fatma Abdelhedi, Hanen Sellami, et al.
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