M. Miladi

Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity

N. Elleuch, A. Brice, G. Stevanin, 2009, Clinical genetics.

[A novel mutation in ATP7B gene associated with severe neurological impairment in Wilson's disease].

F. Woimant, A. Boukhris, C. Mhiri, 2010, Revue neurologique.

Sacral meningeal arteriovenous fistula supplied by branches of the hypogastric artery revealed by conus medullaris infarction

C. Mhiri, C. Triki, M. Kechaou, 2000, Spinal Cord.

Selective bilateral thalamic necrosis following carbon monoxide poisoning: Case report

A. Boukhris, C. Mhiri, I. Fki, 2013, Journal of Neurological Sciences.