Authors: Barhoumi, C Amouri, R Ben Hamida, C Ben Hamida, M Machghoul, S Gueddiche, M Hentati, F

Citation: C. Barhoumi et al., Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3, NEUROMUSC D, 11(1), 2001, pp. 27-34

Authors: Nicole, S Davoine, CS Topaloglu, H Cattolico, L Barral, D Beighton, P Ben Hamida, C Hammouda, H Cruaud, C White, PS Samson, D Urtizberea, JA Lehmann-Horn, F Weissenbach, J Hentati, F Fontaine, B

Citation: S. Nicole et al., Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia), NAT GENET, 26(4), 2000, pp. 480-483

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: Decary, S Ben Hamida, C Mouly, V Barbet, JP Hentati, F Butler-Browne, GS

Citation: S. Decary et al., Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children, NEUROMUSC D, 10(2), 2000, pp. 113-120

Authors: Mrissa, N Belal, S Ben Hamida, C Amouri, R Turki, I Mrissa, R Ben Hamida, M Hentati, F

Citation: N. Mrissa et al., Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxiain a Tunisian family, NEUROLOGY, 54(7), 2000, pp. 1408-1414