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

Mixed movement disorders revealing an atypical form of creatine deficiency syndrome

por Nasrallah, Fahmi, Benrhouma, Hanene, Kraoua, Ichraf, Briand, Gilbert, Omar, Souheil, Turki Ben Youssef, Ilhem, Kaabachi, Naziha
Publicado 2015

Rasmussen's Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review

por Klaa, Hedia, Ben Younes, Thouraya, Benrhouma, Hanene, Nagi, Sonia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef-Turki, Ilhem
Publicado 2020

Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years

por Ben Achour, Nedia, Rebai, Ibtihel, Raddadi, Sarra, Benrhouma, Hanene, Klaa, Hedia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef Turki, Ilhem
Publicado 2017

Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort

por Douma, Bissene, Ben Younes, Thouraya, Benrhouma, Hanene, Miladi, Zouhour, Zamali, Imen, Rouissi, Aida, Klaa, Hedia, Kraoua, Ichraf, Ben Ahmed, Melika, Ben Youssef Turki, Ilhem
Publicado 2021

Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia

por Kraoua, Ichraf, Karkar, Adnane, Drissi, Cyrine, Benrhouma, Hanene, Klaa, Hedia, Samaan, Simon, Renaldo, Florence, Elmaleh, Monique, Ben Hamouda, Mohamed, Abdelhak, Sonia, Boespflug‐Tanguy, Odile, Ben Youssef‐Turki, Ilfghem, Dorboz, Imen
Publicado 2019