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

by Imen Rejeb, Houweyda Jilani, Yasmina Elaribi, Syrine Hizem, Lamia Hila, Julia Lauer Zillahrdt, Jamel Chelly, Lamia Benjemaa
Published 2017-11-01

The phenotypic spectrum in a patient with Glycine to Serine mutation in the COL2A1 gene: overview study

by Mohammad Shboul, Hela Sassi, Houweyda Jilani, Imen Rejeb, Yasmina Elaribi, Syrine Hizem, Lamia Ben Jemaa, Marwa Hilmi, Susanna Gerit Kircher, Ali Al Kaissi
Published 2021-02-01

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

by Imen Rejeb, Mouna Jerbi, Houweyda Jilani, Hanène Gaied, Yasmina Elaribi, Syrine Hizem, Raja Aoudia, Hafedh Hedri, Chiraz Zaied, Salwa Abid, Hassen Bacha, Taieb BenAbdallah, Lamia BenJemaa, Rim Goucha
Published 2021-06-01