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Laboratory Medicine|January 6, 2025
Detection of multiple myositis-specific antibodies: prevalence and clinical significanceAmeni Jerbi, Sahar Karoui, Mouna Snoussi, et al.
Romanian Journal of Internal Medicine = Revue Roumaine De Medecine Interne|November 10, 2023
Clinical features and outcomes in patients with human immunodeficiency virus-negative, Castleman's disease: a single medical center study in TunisiaImen Chabchoub, Raida Ben Salah, Rim Kallel, et al.
La Tunisie Medicale|September 19, 2012
[Pregnancy in dermatomyositis and polymyositis]Neila Kaddour, Mouna Snoussi, Sameh Marzouk, et al.
The Pan African Medical Journal|February 4, 2017
[Liver involvement in Rendu-Osler disease: a case report and review of literature]Hanen Loukil, Mouna Snoussi, Hela Fourati, et al.
Caspian Journal of Internal Medicine|December 5, 2017
A challenging entity: multiple sclerosis or collagen tissue disorders: A case series of 6 patientsRaida Ben Salah, Yosra Cherif, Faten Frikha, et al.
International Journal of Immunogenetics|June 20, 2023
ICOS gene polymorphisms in systemic lupus erythematosus: A case-control studyHana Houssaini, Emna Bouallegui, Olfa Abida, et al.
Clinical Case Reports|August 22, 2022
Cavitary lung opacity of unusual cause during Behçet diseaseDonia Chebbi, Chifa Damak, Faten Frikha, et al.
Presse Medicale (Paris, France : 1983)|October 27, 2019
Clinical and serological profile of systemic sclerosis in Tunisia: A retrospective observational studyRaida Ben Salah, Faten Frikha, Hend Hachicha, et al.
European Journal of Drug Metabolism and Pharmacokinetics|June 17, 2015
Genetic Determinants of Methotrexate Toxicity in Tunisian Patients with Rheumatoid Arthritis: A Study of Polymorphisms Involved in the MTX Metabolic PathwaySouhir Chaabane, Sameh Marzouk, Rim Akrout, et al.
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