1. Acquired demyelinating syndromes of the central nervous system in children: study of a cohort of 47 cases. (June 2017) Authors: Ben Achour, N.; Raddadi, S.; Benrhouma, H.; Klaa, H.; Rouissi, A.; Kraoua, I.; Ben Youssef Turki, I. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical presentations of Guillain-Barré Syndrome in children. (June 2017) Authors: El Mabrouk, E.; Ben Achour, N.; Turki, A.; Benrhouma, H.; Klaa, H.; Kraoua, I.; Ben Youssef-Turki, I. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e230 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Infantile and childhood onset PLA2G6‐associated neurodegeneration in a large North African cohort. (27th August 2014) Authors: Romani, M.; Kraoua, I.; Micalizzi, A.; Klaa, H.; Benrhouma, H.; Drissi, C.; Turki, I.; Castellana, S.; Mazza, T.; Valente, E. M.; Gouider‐Khouja, N. Journal: European journal of neurology Issue: Volume 22:Number 1(2015:Jan.) Page Start: 178 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. SQSTM1 mutation: Description of the first Tunisian case and literature review. Issue 12 (2nd November 2020) Authors: Akkari, M.; Kraoua, I.; Klaa, H.; Benrhouma, H.; Ben Younes, T.; Rouissi, A.; Chaabouni, M.; Ben Youssef‐Turki, I. Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗