Ngā hua rapu - Lobna Boussofara

Recurrent acute generalized exanthematous pustulosis to two different drugs: Oxacillin and Dextromethorphan confirmed by patch test mā zied kenani, Rima Gammoudi, Neila Fathallah, Amina Aounallah, Sana Mokni, Nejet Ghariani, Colandane Belajouza, Chaker Ben Salem, Mohamed Denguezli, Lobna Boussofara

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Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene mā Hamza Chouk, Mohamed Ben Rejeb, Lobna Boussofara, Haїfa Elmabrouk, Najet Ghariani, Badreddine Sriha, Ali Saad, Dorra H’Mida, Mohamed Denguezli

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Diagnostic challenge in a series of eleven patients with hyper IgE syndromes mā Roukaya Yaakoubi, Roukaya Yaakoubi, Najla Mekki, Najla Mekki, Imen Ben-Mustapha, Imen Ben-Mustapha, Leila Ben-Khemis, Asma Bouaziz, Ilhem Ben Fraj, Jamel Ammar, Agnès Hamzaoui, Hamida Turki, Lobna Boussofara, Mohamed Denguezli, Samir Haddad, Monia Ouederni, Mohamed Bejaoui, Koon Wing Chan, Yu Lung Lau, Fethi Mellouli, Mohamed-Ridha Barbouche, Mohamed-Ridha Barbouche, Meriem Ben-Ali

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