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

door Chograni, Manèl, Rejeb, Imen, Jemaa, Lamia Ben, Châabouni, Myriam, Bouhamed, Habiba Chaabouni
Gepubliceerd in 2011

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

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

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

door 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
Gepubliceerd in Afr J Emerg Med (2021)

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

door 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
Gepubliceerd in BMC Med Genomics (2021)

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

door 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
Gepubliceerd in Eur J Hum Genet (2016)