Craniosynostosis, Scheuermann's disease, and intellectual disability resembling Shprintzen–Goldberg syndrome: a report on a family over 4 generations: Case report

por Al Kaissi, Ali, Marrakchi, Zahra, Nassib, Nabil M., Hofstaetter, Jochen, Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2017

Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar Syndrome

por Najjar, Dorra, Chikhaoui, Asma, Zarrouk, Sinda, Azouz, Saifeddine, Kamoun, Wafa, Nassib, Nabil, Bouchoucha, Sami, Yacoub-Youssef, Houda
Publicado 2022

Torticollis in Connection with Spine Phenotype

por Al Kaissi, Ali, Nassib, Nabil, Bouchoucha, Sami, Shboul, Mohammad, Grill, Franz, Kircher, Susanne Gerit, Ochirova, Polina, Ryabykh, Sergey
Publicado 2022

Are parents of children with Cockayne syndrome manifesting features of the disorder?: Case reports

por Al Kaissi, Ali, Kuranova, Mirya, Pleskach, Nadezhda, Kenis, Vladimir, Nassib, Nabil M., Grill, Franz, Ganger, Rudolf, Gerit Kircher, Susanne
Publicado 2017

Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities

por Al Kaissi, Ali, Ryabykh, Sergey, Nassib, Nabil, Bouchoucha, Sami, Benjemaa, Lamia, Rejeb, Imen, Hizem, Syrine, Kenis, Vladimir, Grill, Franz, Kircher, Susanne Gerit, Shboul, Mohammad, Ben Chehida, Farid
Publicado 2022

How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports

por Al Kaissi, Ali, Windpassinger, Christian, Chehida, Farid Ben, Ghachem, Maher Ben, Nassib, Nabil M., Kenis, Vladimir, Melchenko, Eugene, Morenko, Ekatrina, Ryabykh, Sergey, Hofstaetter, Jochen G., Grill, Franz, Ganger, Rudolf, Kircher, Susanne Gerit
Publicado 2017