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Gene|November 1, 2024
Gardner syndrome in a Tunisian family: Identification of a rare APC mutation through targeted NGSRania Abdelmaksoud-Dammak, Nihel Ammous-Boukhris, Souhir Guidara, et al.
Seizure|November 11, 2017
HLA-A*31:01 and carbamazepine-induced DRESS syndrom in a sample of North African populationKamilia Ksouda, Hanen Affes, Nedia Mahfoudh, et al.
Indian Journal of Nephrology|January 4, 2024
Dorfman-Chanarin Syndrome with Renal Involvement: A Rare Case Report and Literature ReviewIkram Agrebi, Achraf Jaziri, Houda Kanoun, et al.
Future Science OA|June 6, 2024
Effect of long-term proton pump inhibitors on phosphocalcium metabolism and bone mineral densityHend Smaoui, Lassaad Chtourou, Dana Jallouli, et al.
Acta Histochemica|December 3, 2011
Expression of COX-2 and E-cadherin in Tunisian patients with colorectal adenocarcinomaImen Miladi-Abdennadher, Rania Abdelmaksoud-Dammak, Dorra Ben Ayed-Guerfali, et al.
Laboratory Medicine|February 17, 2023
Biclonal Gammopathies in South Tunisia: Clinical and Biological CharacteristicsAmeni Jerbi, Hend Hachicha, Aida Charfi, et al.
F1000Research|September 28, 2023
EncephalApp Stroop Test for covert hepatic encephalopathy screening in Tunisian cirrhotic patientsLamine Hamzaoui, Moufida Mahmoudi, Ghanem Mohamed, et al.
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