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Results: 1-9 |
Results: 9
Effect of vitamin E supplementation in patients with ataxia with vitamin Edeficiency
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
Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families
Authors: Marzouki, N Belal, S Benhamida, C Benlemlih, M Hentati, F
Citation: N. Marzouki et al., Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families, CLIN GENET, 59(4), 2001, pp. 257-262
Intrafamilial phenotypic variability of Hallervorden-Spatz syndrome in a Tunisian family
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
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Authors: Bomont, P Cavalier, L Blondeau, F Hamida, CB Belal, S Tazir, M Demir, E Topaloglu, H Korinthenberg, R Tuysuz, B Landrieu, P Hentati, F Koenig, M
Citation: P. Bomont et al., The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy, NAT GENET, 26(3), 2000, pp. 370-374
Giant axonal neuropathy locus refinement to a < 590 kb critical interval
Authors: Cavalier, L BenHamida, C Amouri, R Belal, S Bomont, P Lagarde, N Gressin, L Callen, D Demir, E Topaloglu, H Landrieu, P Ioos, C Ben Hamida, M Koenig, M Hentati, F
Citation: L. Cavalier et al., Giant axonal neuropathy locus refinement to a < 590 kb critical interval, EUR J HUM G, 8(7), 2000, pp. 527-534
Clinical and genetic study of familial Parkinson's disease in Tunisia
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
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxiain a Tunisian family
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
Linkage disequilibrium at the SCA2 locus
Authors: Didierjean, O Cancel, G Stevanin, G Durr, A Burk, K Benomar, A Lezin, A Belal, S Abada-Bendid, M Klockgether, T Brice, A
Citation: O. Didierjean et al., Linkage disequilibrium at the SCA2 locus, J MED GENET, 36(5), 1999, pp. 415-417
Juvenile form of dihydropteridine reductase deficiency in 2 tunisian patients
Authors: Larnaout, A Belal, S Miladi, N Kaabachi, N Mebazza, A Dhondt, JL Hentati, F
Citation: A. Larnaout et al., Juvenile form of dihydropteridine reductase deficiency in 2 tunisian patients, NEUROPEDIAT, 29(6), 1998, pp. 322-323
Risultati: 1-9 |