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

Por Chograni, Manèl, Rejeb, Imen, Jemaa, Lamia Ben, Châabouni, Myriam, Bouhamed, Habiba Chaabouni
Publicado em 2011

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

Por Rejeb, Imen, Jilani, Houweyda, Elaribi, Yasmina, Hizem, Syrine, Hila, Lamia, Zillahrdt, Julia Lauer, Chelly, Jamel, Benjemaa, Lamia
Publicado no BMC Med Genet (2017)

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

Por 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
Publicado no Afr J Emerg Med (2021)

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

Por 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
Publicado no Eur J Hum Genet (2016)