Authors: Gabsi, S Gouider-Khouja, N Belal, S Fki, M Kefi, M Turki, I Ben Hamida, M Kayden, H Mebazaa, R Hentati, F

Citation: S. Gabsi et al., Effect of vitamin E supplementation in patients with ataxia with vitamin Edeficiency, EUR J NEUR, 8(5), 2001, pp. 477-481

Authors: Gouider-Khouja, N Miladi, N Belal, S Hentati, F

Citation: N. Gouider-khouja et al., Intrafamilial phenotypic variability of Hallervorden-Spatz syndrome in a Tunisian family, PARKINS R D, 6(3), 2000, pp. 175-179

Authors: Gouider-Khouja, N Gabsi, S Khouja, N Hentati, F

Citation: N. Gouider-khouja et al., Hemiparkinsonian syndrome due to a cerebral tumor infiltrating the substantia nigra, PARKINS R D, 6(2), 2000, pp. 115-117

Authors: Driss, A Amouri, R Ben Hamida, C Souilem, S Gouider-Khouja, N Ben Hamida, M Hentati, F

Citation: A. Driss et al., A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3, NEUROMUSC D, 10(4-5), 2000, pp. 240-246

Authors: Gouider-Khouja, N Belal, S Ben Hamida, M Hentati, F

Citation: N. Gouider-khouja et al., Clinical and genetic study of familial Parkinson's disease in Tunisia, NEUROLOGY, 54(8), 2000, pp. 1603-1609