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

بواسطة Chograni, Manèl, Rejeb, Imen, Jemaa, Lamia Ben, Châabouni, Myriam, Bouhamed, Habiba Chaabouni
منشور في 2011

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

بواسطة Rejeb, Imen, Jilani, Houweyda, Elaribi, Yasmina, Hizem, Syrine, Hila, Lamia, Zillahrdt, Julia Lauer, Chelly, Jamel, Benjemaa, Lamia
الحاوية / القاعدة BMC Med Genet (2017)

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

بواسطة 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
الحاوية / القاعدة Afr J Emerg Med (2021)

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

بواسطة 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
الحاوية / القاعدة BMC Med Genomics (2021)

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

بواسطة 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
الحاوية / القاعدة Eur J Hum Genet (2016)