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

Autor Chograni, Manèl, Rejeb, Imen, Jemaa, Lamia Ben, Châabouni, Myriam, Bouhamed, Habiba Chaabouni
Vydáno 2011

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

Autor Rejeb, Imen, Jilani, Houweyda, Elaribi, Yasmina, Hizem, Syrine, Hila, Lamia, Zillahrdt, Julia Lauer, Chelly, Jamel, Benjemaa, Lamia
Vydáno v BMC Med Genet (2017)

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

Autor 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
Vydáno v Afr J Emerg Med (2021)

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

Autor 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
Vydáno v BMC Med Genomics (2021)

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

Autor 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
Vydáno v Eur J Hum Genet (2016)