The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly

by Chograni, Manèl, Rejeb, Imen, Jemaa, Lamia Ben, Châabouni, Myriam, Bouhamed, Habiba Chaabouni
Published 2011

First case report of Cohen syndrome in the Tunisian population caused by VPS13B mutations

by Rejeb, Imen, Jilani, Houweyda, Elaribi, Yasmina, Hizem, Syrine, Hila, Lamia, Zillahrdt, Julia Lauer, Chelly, Jamel, Benjemaa, Lamia
Published in BMC Med Genet (2017)

Stroke knowledge among emergency centre visitors: A cross-sectional multicenter survey

by Chakroun-Walha, Olfa, Samet, Amal, Ben Abdallah, Marwa, Benmansour, Sana, Issaoui, Fadhila, Rebai, Manel, Ben Messaoud, Karama, Benali, Cyrine, Mokni, Wassel, Nasri, Abdennour, Rejeb, Imen, Rekik, Noureddine
Published in Afr J Emerg Med (2021)

New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 gene

by Rejeb, Imen, Jerbi, Mouna, Jilani, Houweyda, Gaied, Hanène, Elaribi, Yasmina, Hizem, Syrine, Aoudia, Raja, Hedri, Hafedh, Zaied, Chiraz, Abid, Salwa, Bacha, Hassen, BenAbdallah, Taieb, BenJemaa, Lamia, Goucha, Rim
Published in BMC Med Genomics (2021)

Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

by Zillhardt, Julia Lauer, Poirier, Karine, Broix, Loïc, Lebrun, Nicolas, Elmorjani, Adrienne, Martinovic, Jelena, Saillour, Yoann, Muraca, Giuseppe, Nectoux, Juliette, Bessieres, Bettina, Fallet-Bianco, Catherine, Lyonnet, Stanislas, Dulac, Olivier, Odent, Sylvie, Rejeb, Imen, Jemaa, Lamia Ben, Rivier, Francois, Pinson, Lucile, Geneviève, David, Musizzano, Yuri, Bigi, Nicole, Leboucq, Nicolas, Giuliano, Fabienne, Philip, Nicole, Vilain, Catheline, Van Bogaert, Patrick, Maurey, Hélène, Beldjord, Cherif, Artiguenave, François, Boland, Anne, Olaso, Robert, Masson, Cécile, Nitschké, Patrick, Deleuze, Jean-François, Bahi-Buisson, Nadia, Chelly, Jamel
Published in Eur J Hum Genet (2016)