I. Rebai

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood

N. Gouider-Khouja, H. Klaa, A. Rouissi, 2015, Brain and Development.

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

H. Benrhouma, H. Klaa, A. Rouissi, 2017, BioMed research international.

Childhood opsoclonus–myoclonus syndrome: A case series from Tunisia

I. Turki, S. Mrabet, H. Benrhouma, 2017, Brain and Development.

Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review.

M. Ben Ahmed, I. Kraoua, I. Rebai, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review

C. Drissi, O. Boespflug-Tanguy, S. Abdelhak, 2021, Neuropediatrics.

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

C. Drissi, N. Gouider-Khouja, H. Benrhouma, 2013, Iranian journal of child neurology.

Seronegative myasthenia gravis with bladder dysfunction.

I. Marouani, N. Gouider-Khouja, I. Turki, 2012, Revue neurologique (Paris).