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American Journal of Human Genetics|June 3, 2017
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in HumansLisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, et al.
Experimental Dermatology|April 28, 2023
miRNA implication in the pathogenesis and the outcome of Tunisian endemic pemphigus foliaceusBoudour Khabou, Raouia Fakhfakh, Safa Tahri, et al.
Molecular Genetics & Genomic Medicine|November 9, 2022
Evaluation of X chromosome inactivation in endemic Tunisian pemphigus foliaceusOlfa Abida, Nesrine Elloumi, Emna Bahloul, et al.
Immunology Letters|February 21, 2017
Role of FOXP3 gene polymorphism in the susceptibility to Tunisian endemic Pemphigus FoliaceusMariem Ben Jmaa, Olfa Abida, Emna Bahloul, et al.
Steroids|June 15, 2024
Unraveling the role of the vitamin D-VDR pathway in pemphigus vulgaris from Tunisian patientsFatma Dhaffouli, Nesrine Elloumi, Safa Tahri, et al.
International Journal of Dermatology|July 17, 2018
Pemphigus herpetiformis in South Tunisia: a clinical expression of pemphigus foliaceus?Ameni Jerbi, Hend Hachicha, Sawsan Feki, et al.
Nephrologie & Therapeutique|July 1, 2022
[Cutaneous leishmaniasis after renal transplantation: Report of 7 cases and review of the literature]Soumaya Yaich, Hanen Abid, Salma Toumi, et al.
Clinical Case Reports|January 26, 2022
Compound blue nevus: A misleading pigmented melanocytic tumorMassara Baklouti, Khadija Sellami, Neila Elleuch, et al.
Orphanet Journal of Rare Diseases|May 24, 2019
Thyroid involvement in Chanarin-Dorfman syndrome in adults in the largest series of patients carrying the same founder mutation in ABHD5 geneNacim Louhichi, Emna Bahloul, Slaheddine Marrakchi, 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.
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