ACETAMINOPHEN-INDUCED CELLULITIS-LIKE FIXED DRUG ERUPTION

por Fathallah, Neila, Salem, Chaker Ben, Slim, Raoudha, Boussofara, Lobna, Ghariani, Najet, Bouraoui, Kamel
Publicado 2011

Co-amoxiclav-induced Stevens Johnson Syndrome in a child

por Fathallah, Neila, Hanen, Zayani, Slim, Raoudha, Boussofara, Lobna, Najet, Ghariani, Bouraoui, Kamel, Salem, Chaker Ben
Publicado 2013

Recurrent Acute Generalized Exanthematous Pustulosis to Two Different Drugs: Oxacillin and Dextromethorphan Confirmed by Patch Test

por Kenani, Zied, Gammoudi, Rima, Fathallah, Neila, Aounallah, Amina, Mokni, Sana, Boussofara, Lobna, Ghariani, Nejet, Belajouza, Colandane, Ben Salem, Chaker, Denguezli, Mohamed
Publicado 2022

Forme particulière de Pemphigoide cicatricielle à dépôt unique d'IgA

por Aounallah, Amina, Jrad, Mariem, Ksiaa, Mehdi, Mokni, Sana, Saidi, Wafa, Boussofara, Lobna, Sriha, Badreddine, Denguezli, Mohamed, Ghariani, Najet, Belajouza, Colandane, Nouira, Rafia
Publicado 2017

Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

por Chouk, Hamza, Ben Rejeb, Mohamed, Boussofara, Lobna, Elmabrouk, Haїfa, Ghariani, Najet, Sriha, Badreddine, Saad, Ali, H’Mida, Dorra, Denguezli, Mohamed
Publicado 2021

A novel AIRE gene mutation in a patient with autoimmune polyendocrinopathy candidiasis and ectodermal dystrophy revealed by alopecia areata

por Arousse, Aycha, Boussofara, Lobna, H'mida-Ben Brahim, Dorra, Migaud, Mélanie, Aounallah, Amina, Ghariani, Najet, Casanova, Jean-Laurent, Nouira, Rafiaa, Puel, Anne, Denguezli, Mohamed
Publicado 2018

Multiple Self-Healing Palmoplantar Carcinoma: A Familial Predisposition to Skin Cancer with Primary Palmoplantar and Conjunctival Lesions

por Mamaï, Ons, Boussofara, Lobna, Denguezli, Mohamed, Escande-Beillard, Nathalie, Kraeim, Wahiba, Merriman, Barry, Ben Charfeddine, Ilhem, Stevanin, Giovanni, Bouraoui, Sana, Amara, Abdelbasset, Mili, Amira, Nouira, Rafiaa, H'mida, Dorra, Sriha, Badreddine, Gribaa, Moez, Saad, Ali, Reversade, Bruno
Publicado 2015

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

por Yaakoubi, Roukaya, Mekki, Najla, Ben-Mustapha, Imen, Ben-Khemis, Leila, Bouaziz, Asma, Ben Fraj, Ilhem, Ammar, Jamel, Hamzaoui, Agnès, Turki, Hamida, Boussofara, Lobna, Denguezli, Mohamed, Haddad, Samir, Ouederni, Monia, Bejaoui, Mohamed, Chan, Koon Wing, Lau, Yu Lung, Mellouli, Fethi, Barbouche, Mohamed-Ridha, Ben-Ali, Meriem
Publicado 2023

Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma

por Pohler, Elizabeth, Mamai, Ons, Hirst, Jennifer, Zamiri, Mozheh, Horn, Helen, Nomura, Toshifumi, Irvine, Alan D., Moran, Benvon E., Wilson, Neil J., Smith, Frances J. D., Goh, Christabelle S. M, Sandilands, Aileen, Cole, Christian, Barton, Geoffrey J., Evans, Alan T., Shimizu, Hiroshi, Akiyama, Masashi, Suehiro, Akihiro, Konohana, Izumi, Shboul, Mohammad, Teissier, Sebastien, Boussofara, Lobna, Denguezli, Mohamed, Saad, Ali, Gribaa, Moez, Dopping-Hepenstal, Patricia J., McGrath, John A, Brown, Sara J., Goudie, David R., Reversade, Bruno, Munro, Colin S., McLean, W. H. Irwin
Publicado 2012