Mirror Movements and Myelomeningocele: Report of A Single Case and Review of Literature

por RéBAI, Ibtihel, BENRHOUMA, Hanene, KRAOUA, Ichraf, DRISSI, Cyrine, Ben HAMMOUDA, Mohammed, GOUIDER-KHOUJA, Neziha
Publicado 2013

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

por Khadija, Bochra, Rjiba, Khouloud, Dimassi, Sarra, Dahleb, Wafa, Kammoun, Molka, Hannechi, Hanen, Miladi, Najoua, Gouider-khouja, Neziha, Saad, Ali, Mougou-Zerelli, Soumaya
Publicado 2022

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

por Romani, Marta, Micalizzi, Alessia, Kraoua, Ichraf, Dotti, Maria Teresa, Cavallin, Mara, Sztriha, László, Ruta, Rosario, Mancini, Francesca, Mazza, Tommaso, Castellana, Stefano, Hanene, Benrhouma, Carluccio, Maria Alessandra, Darra, Francesca, Máté, Adrienn, Zimmermann, Alíz, Gouider-Khouja, Neziha, Valente, Enza Maria
Publicado 2014